CA2501984C - Erythropoietin receptor binding antibodies - Google Patents

Abstract

The present invention relates to antibodies and antibody fragments thereof that bind to and activate an erythropoietin receptor. The present invention also relates to methods of modulating the endogenous activity of an erythropoietin receptor in a mammal using said antibodies as well as pharmaceutical compositions containing said antibodies.

Description

ERYTHROPOIETIN RECEPTOR BINDING ANTIBODIES

Technical Field of the Invention The present invention relates to antibodies that recognize, bind to and, preferably, activate the erythropoietin receptor.

Background of the Invention Erythropoietin ("EPO") is a glycoprotein that is the primary regulator of erythropoiesis.
Specifically, EPO is responsible for promoting the growth, differentiation and survival of erythroid progenitors, which give rise to mature red blood cells. In response to changes in the level of oxygen in the blood and tissues, erythropoietin appears to stimulate both proliferation and differentiation of immature erythroblasts. It also functions as a growth factor, stimulating the mitotic activity of erythroid progenitor. cells, such as erythrocyte burst forming and colony-forming units. It also acts as a differentiation factor, triggering transformation of an erythrocyte colony-forming-unit into a proerythroblast (See Erslev, A., New Eng. J. Med., 316:101-103 (1987)).

EPO has a molecular weight of about 34,000 daltons and can occur in three forms -alpha, beta and asialo. During mid- to late gestation, EPO is synthesized in the fetal liver.
Subsequently, EPO is synthesized in the kidney, circulates in the plasma and is excreted in the urine.

Human urinary EPO has been isolated and purified (See, Miyake et al., J. Biol.
Chem., 252:5558 (1977)). Moreover, methods for identifying, cloning and expressing genes encoding EPO (See U.S. Patent 4,703,008) as well as purifying recombinant EPO from a cell medium (See U.S. Patent 4,667,016) are known in the art.

The activity of EPO is mediated through the binding and activation of a cell surface receptor referred to as the erythropoietin receptor. The EPO receptor belongs to the cytokine receptor superfamily and is believed to contain at least two distinct polypeptides, a 55-72 kDa species and a 85-100 kDa species (See U.S. Patent 6,319,499, Mayeux et al., J.
Biol. Chem, 266:23380 (1991), McCaffery et al., J Biol. Chem., 264:10507 (1991)). Other studies have revealed other polypeptide complexes of EPO receptor having molecular weights such as 110, 130 and 145 kDa (See U.S. Patent 6,319,499).

Both the murine and human EPO receptors have been cloned and expressed (See D'Andrea et al., Cell, 57:277 (1989); Jones et al., Blood, 76:31 (1990);
Winkelmann et al., Blood, 76:24 (1990); WO 90/08822/ U.S. Patent 5,278,065). The full length human EPO
receptor is a 483 amino acid transmembrane protein with an approximately 25 amino acid signal peptide (See U.S. Patent 6,319,499). The human receptor demonstrates about a 82%
amino acid sequence homology with the murine receptor. Id.
In the absence of ligand the EPO receptor exists in a preformed dimer. The binding of EPO to its receptor causes a conformational change such that the cytoplasmic domains are placed in close proximity. While not completely understood, it is believed that this "dimerization" plays a role in the activation of the receptor. The activation of the EPO receptor results in a number of biological effects. Some of these activities include stimulation of proliferation, stimulation of differentiation and inhibition of apoptosis (See U.S. Patent 6,319,499, Liboi et al., PNAS USA, 90:11351 (1993), Koury, Science, 248:378 (1990)).

It is the relationship between the EPO receptor dimerization and activation that can be used to identify compounds (i.e. such as antibodies) other than EPO that are capable of: (1) dimerizing the EPO receptor; and (2) activating the receptor. These compounds would be useful in treating mammals suffering from anemia and in identifying mammals having a dysfunctional EPO receptor.

Summary of the Invention In one embodiment, the invention relates to antibodies that bind to the human erythropoietin receptor. In one embodiment, the antibodies comprise a heavy chain variable region that is selected from the group consisting of SEQ ID NOS: 3, 7, 11, 15, 19, 31, 35, 39, 43, 47, 51, 55 and fragments thereof. In another embodiment, the antibodies comprise a light chain variable region that is selected from the group consisting of SEQ ID
NOS: 5, 9, 13, 17, 21, 23, 25, 27, 29, 33, 37, 41, 45, 49, 53, 57 and fragments thereof.

In another embodiment, the present invention relates to an isolated antibody that is capable of binding a human erythropoietin receptor in a mammal. Such an antibody comprises a heavy chain variable region or a light chain variable region that comprises a continuous sequence from CDRl through CDR3. The amino acid sequence of the heavy chain variable region comprising the continuous sequence from CDRl through CDR3 is selected from the group consisting of: SEQ ID NO:58, SEQ ID NO:59, SEQ ID NO:60, SEQ ID NO:61 and fragments thereof. The amino acid sequence of the light chain variable region comprising the continuous sequence from CDRl through CDR3 is selected from the group consisting of. SEQ
ID NO:62, SEQ ID NO:63, SEQ ID NO:64, SEQ ID NO:65, SEQ ID NO:66, SEQ ID
NO:67, SEQ ID NO:68 and fragments thereof.

In another embodiment, the present invention relates to an antibody that activates an endogenous activity of a human erythropoietin receptor in a mammal but does not interact with a peptide having an amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV
(SEQ ID NO:1).

In another embodiment, the present invention relates to an antibody that is capable of activating an endogenous activity of a human erythropoietin receptor in a mammal, wherein said antibody or antibody fragment thereof exhibits a binding affinity within one hundred fold of the binding affinity of endogenous human erythropoietin to the erythropoietin receptor.

In yet another embodiment, the present invention relates to an antibody or antibody fragment thereof that activates an endogenous activity of a human erythropoietin receptor in a mammal. The antibody or antibody fragment thereof comprises at least one human heavy chain variable region having the amino acid sequence of SEQ ID NO:3 or antibody fragment thereof, and/or at least one human light chain variable region having the amino acid sequence of SEQ ID NO:5 or antibody fragment thereof, provided that said antibody or antibody fragment thereof does not interact with a peptide having an amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV (SEQ ID NO:1).

In yet another embodiment, the present invention relates to an antibody or antibody fragment thereof that activates an endogenous activity of a human erythropoietin receptor in a mammal. The antibody or antibody fragment thereof comprises at least one heavy chain variable region having the amino acid sequence of SEQ ID NO:7 or antibody fragment thereof, and/or at least one light chain variable region having the amino acid sequence of SEQ ID NO:9 or antibody fragment thereof, provided that said antibody or antibody fragment thereof does not interact with a peptide having an amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV (SEQ ID NO:1).

This embodiment also includes other heavy chain variable regions selected from the group consisting of SEQ ID NO: 11, 15, 19, 31, 35, 39, 43, 47, 51, and 55 or an antibody fragment of any of these aforementioned SEQ ID NOS, wherein said antibody or antibody fragment thereof does not interact with a peptide having an amino acid sequence of SEQ ID
NO: 1. Other light chain variable regions included in this embodiment may be selected from the group consisting of SEQ ID NO: 13, 17, 21, 23, 25, 27, 29, 33, 37, 41, 45, 49, 53 and 57 or an antibody fragment of any of these aforementioned SEQ ID NOS, wherein said antibody or antibody fragment thereof does not interact with a peptide having an amino acid sequence of SEQ ID NO: 1.

In yet another embodiment, the invention provides an antibody or antibody fragment thereof that activates an endogenous activity of a human erythropoietin receptor in a mammal, the antibody comprising the amino acid sequences of at least one heavy chain variable region and at least one light chain variable region selected from the group consisting of SEQ ID
NO:11/SEQ ID NO:13, SEQ ID NO:15/SEQ ID NO:17, SEQ ID NO:19/SEQ ID NO:21, SEQ
ID NO:11/SEQ ID NO:23,'SEQ ID NO: 11/SEQ ID NO:25, SEQ ID NO:11/SEQ ID NO:27, SEQ ID NO:11/SEQ ID NO:29, SEQ ID NO:31/SEQ ID NO:33, SEQ ID NO:35/SEQ ID
NO:37, SEQ ID NO:39/SEQ ID NO:41, SEQ ID NO:43/SEQ ID NO:45, SEQ ID NO:47/SEQ
ID NO:49, SEQ ID NO:51/SEQ ID NO:53 and SEQ ID NO:55/SEQ ID NO:57 or antibody fragment thereof, wherein said antibody or antibody fragment thereof does not interact with a peptide having an amino acid sequence of SEQ ID NO: 1.

In yet another embodiment, the present invention relates to a method of activating an endogenous activity of a human erythropoietin receptor in a mammal. The method involves the step of administering to a mammal a therapeutically effective amount of an antibody or antibody fragment thereof to activate the EPO receptor. The antibody or antibody fragment thereof does not interact with a peptide having an amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV (SEQ ID NO:1).
In yet a further embodiment, the present invention relates to a method of modulating an endogenous activity of a human erythropoietin receptor in a mammal. The method involves administering to a mammal a therapeutically effective amount of an antibody or antibody fragment thereof to modulate the endogenous activity of a human erythropoietin receptor in a mammal but does not interact with a peptide having an amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV (SEQ ID NO:1).

In yet a further embodiment, the present invention relates to a method of treating a mammal suffering from pure red cell aplasia induced by neutralizing anti-erythropoietin antibodies. The method involves administering to a mammal in need of treatment a therapeutically effective amount of an antibody or antibody fragment thereof to activate said receptor, wherein said antibody or antibody fragment thereof does not interact with a peptide having an amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV (SEQ ID NO:1).
In yet a further embodiment, the present invention relates to pharmaceutical compositions. The pharmaceutical compositions of the present invention contain a therapeutically effective amount of an antibody or antibody fragment thereof and a pharmaceutically acceptable excipient. The antibody or antibody fragment contained in the pharmaceutical composition activates an endogenous activity of a human erythropoietin receptor in a mammal but does not interact with a peptide having an amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV (SEQ ID NO:1).

In yet a further embodiment, the present invention relates to an IgG2 antibody or antibody fragment that binds to and activates the erythropoietin receptor. The IgG2 antibodies or antibody fragments of this embodiment bind to and interact with any epitope that is involved in activating the EPO receptor. Such antibodies may be polyclonal or monoclonal antibodies or any antibody fragment thereof. The IgG2 antibodies may be chimeric, humanized or human antibodies.

In yet a further embodiment, the present invention provides a method of activating an endogenous activity of a human erythropoietin receptor in a mammal comprising the step of administering to a mammal a therapeutically effective amount of an IgG2 antibody or antibody fragment of the invention to activate the receptor.

In yet a further embodiment, the present invention provides a method of modulating an endogenous activity of a human erythropoietin receptor in a mammal comprising the step of administering to a mammal a therapeutically effective amount of an IgG2 antibody or antibody fragment of the invention to modulate the receptor.

In yet another embodiment, the present invention provides a method of treating a mammal suffering aplasia, the method comprising the step of administering to a mammal in need of treatment a therapeutically effective amount of an IgG2 antibody or antibody fragment of the invention to activate the receptor.

In yet another embodiment, the present invention provides a method of treating a mammal suffering aplasia, the method comprising the step of administering to a mammal in need of treatment a therapeutically effective amount of an IgG2 antibody or antibody fragment of the invention to modulate the receptor.

In yet another embodiment, the present invention provides a pharmaceutical composition comprising a therapeutically effective amount of an IgG2 antibody or antibody fragment of the invention and a pharmaceutically acceptable excipient.

Finally, the present invention relates to isolated and purified polynucleotide and amino acid sequences. The isolated and purified polynucleotide sequences can be selected from the group consisting of. SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ
ID
NO:10, SEQ ID NO:12, SEQ ID NO:14, SEQ ID NO:16, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID
NO:32, SEQ ID NO:34, SEQ ID NO:36, SEQ ID NO:38, SEQ ID NO:40, SEQ ID NO:42, SEQ ID NO:44, SEQ ID NO:46, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID
NO:54, SEQ ID NO:56 and fragments, complements and degenerate codon equivalents thereof.

The present invention further relates to isolated and purified amino acid sequences selected from the group consisting of. SEQ ID NO:3, SEQ ID NO:5, SEQ ID NO:7, SEQ ID
NO:9, SEQ ID NO: 11, SEQ ID NO:13, SEQ ID NO:15, SEQ ID NO:17, SEQ ID NO:19, SEQ
ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:29, SEQ ID NO:31, SEQ ID
NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID
NO:45, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:58, SEQ ID NO:59, SEQ ID NO:60, SEQ ID NO:61, SEQ ID
NO:62, SEQ ID NO:63, SEQ ID NO:64, SEQ ID NO:65, SEQ ID NO:66, SEQ ID NO:67, SEQ ID NO:68 and fragments and complements and thereof.

Brief Description of the Figures Figure 1 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:69 and SEQ ID NO:70, respectively) and amino acid sequence of the heavy chain of human antibody Ab12. The amino acid sequence comprises SEQ ID NOS:71 through 74.
The sequence of the constant region alone is shown as SEQ ID NO:75. The variable chain ends at nucleotide 1283. The variable/constant joining region (underlined) is at nucleotides 1284-1289. The constant region is from nucleotides 1290-2826.

Figure 2 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:76 and SEQ ID NO:77, respectively) and amino acid sequence of the light chain of human antibody Ab12. The amino acid sequence comprises SEQ ID NOS:78. The sequence of the constant region alone is shown as SEQ ID NO: 79. The variable chain ends at nucleotidel363. The variable/constant joining region (underlined) is at nucleotides 1364-1369.
The constant region is from nucleotides 1370-1618.

Figure 3 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:80 and SEQ ID NO:81, respectively) and amino acid sequence of the heavy chain of human antibody Ab198. The amino acid sequence comprises SEQ ID NOS:82 and SEQ ID
NOS 72 through 74. The variable chain ends at nucleotide 1304. The variable/constant joining region (underlined) is at nucleotides 1305-1310. The constant region is from nucleotides 1311-2847.

Figure 4 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:83 and SEQ ID NO:84, respectively) and amino acid sequence of the light chain of human antibody Ab198. The amino acid sequence comprises SEQ ID NOS:78. The variable chain ends at nucleotide 1351. The variable/constant joining region (underlined) is at nucleotides 1352-1357. The constant region is from nucleotides 1358-1606.

Figure 5 shows the competition of Ab12 with 125I-labeled EPO for binding to Chinese Hamster Ovary cells expressing recombinant EPO receptor.

Figure 6 shows the results of an EPO dependent human cell proliferation assay using Abl2 and Ab198.

Figure 7 shows that Ab12 remains active in inducing the proliferation of F36E
cells after storage at 4 C for up to 20 days.

Figure 8 shows that Ab 12 induces the formation of CFU-E (colony forming unit-erythroid) from human 36+ progenitor cells.
Figure 9 shows the induction of proliferation of human erythroid producing cells with Ab198.

Figure 10 shows that Ab198 induces the formation of CFU-E colonies from cynomologous bone marrow-derived erythroid progenitor cells.

Figure 11 shows that Ab 12 does not interact with the peptide SE-3. Ab71A
interacts with the SE-3 peptide.

Figure 12 shows that human Abs secreted by primary hybridomas induce the proliferation of F36E cells.

Figure 13 shows that human Ab supernatants secreted by primary hybridomas interact with intact EPO receptor, but not with peptide SE-3.

Figure 14 shows the activity of various concentrations of Ab12 on the proliferation of UT7/EPO cells.
Figure 15 shows the activity of various concentrations of Ab198 on the proliferation of UT7/EPO cells.

Figure 16 shows the activity of various concentrations of Ab198 (with or without the addition of a secondary goat anti-human FC antibody) on the growth and proliferation of UT7/EPO cells.

Figure 17 shows the activity of various concentrations of Ab12 (with or without the addition of a secondary goat anti-human FC antibody) on the growth and proliferation of UT7/EPO cells.

Figure 18 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-003 of the invention, with Figure 18A (SEQ
ID NO: 10) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 18B (SEQ ID NO:11) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 18A, Figure 18C (SEQ ID NO:12) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 18D (SEQ
ID NO:13) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 18C.

Figure 19 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-012 (also referred to herein as Ab12) of the invention, with Figure 19A (SEQ ID NO:2) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 19B (SEQ ID NO:3) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 19A, Figure 19C (SEQ ID NO:4) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 19D (SEQ ID
NO:5) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 19C.

Figure 20 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-022 of the invention, with Figure 20A (SEQ
ID NO:14) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 20B (SEQ ID NO: 15) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 20A, Figure 20C (SEQ ID NO: 16) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 20D (SEQ
ID NO:17) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 20C.

Figure 21 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-054 of the invention, with Figure 21A (SEQ
ID NO:18) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 21B (SEQ ID NO:19) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 21A, Figure 21C (SEQ ID NO:20) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 21D (SEQ
ID NO:21) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 21 C.

Figure 22 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-060 of the invention, with Figure 22A (SEQ
ID NO:10) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 22B (SEQ ID NO: 11) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 22A, Figure 22C (SEQ ID NO:22) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 22D (SEQ
ID NO:23) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 22C.
Figure 23 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-102 of the invention, with Figure 23A (SEQ
ID NO:10) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 23B (SEQ ID NO: 11) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 23A, Figure 23C (SEQ ID NO:24) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 23D (SEQ
ID NO:25) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 23C.
Figure 24 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-135 of the invention, with Figure 24A (SEQ
ID NO:10) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 24B (SEQ ID NO: 11) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 24A, Figure 24C (SEQ ID NO:26) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 24D (SEQ
ID NO:27) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 24C.
Figure 25 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-145 of the invention, with Figure 25A (SEQ
ID NO:10) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 25B (SEQ ID NO: 11) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 25A, Figure 25C (SEQ ID NO:28) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 25D (SEQ
ID NO:29) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 25C.

Figure 26 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-198 (also referred to herein as Ab198) of the invention, with Figure 26A (SEQ ID NO:6) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 26B (SEQ ID NO:7) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 26A, Figure 26C (SEQ ID
NO:8) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 26D (SEQ ID NO:9) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 26C.

Figure 27 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-254 of the invention, with Figure 27A (SEQ
ID NO:30) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 27B (SEQ ID NO:3 1) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 27A, Figure 27C (SEQ ID NO:32) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 27D (SEQ
ID NO:33) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 27C.

Figure 28 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-267 of the invention, with Figure 28A (SEQ
ID NO:34) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 28B (SEQ ID NO:35) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 28A, Figure 28C (SEQ ID NO:36) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 28D (SEQ
ID NO:37) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 28C.

Figure 29 is a table showing amino acid sequence alignments of heavy chain variable regions of anti-EPOr mAbs generated according to the invention with their associated germline variable region sequences and identifying framework regions and complementarity determining regions.
Figure 30 is a table showing amino acid sequence alignments of light chain variable regions of anti-EPOr mAbs generated according to the invention with their associated germline variable region sequences and identifying framework regions and complementarity determining regions.

Figure 31 is a graph comparing the erythropoietic activity, at various concentrations, of a gamma-1 Ab 12 monoclonal antibody (Mab) and a gamma-2 Ab 12 Mab on an F36e human erythroleukemic cell line.

Figure 32 is a graph showing the increase in percent reticulocyte and percent hematocrit in trangenic mice subjected to a multiple dosing regimen of vehicle, Epogen (5U) or Ab 12 antibody (5 or 50 g).

Figure 33 is a graph showing the increase in percent hematocrit in transgenic mice subjected to a weekly dosing regimen (over 3 weeks) of various concentrations of AranespTM
or Ab 12.

Figure 34 is a graph showing the increase in percent hematocrit in transgenic mice subjected to single versus weekly dosing regimens of various concentrations of AranespTM or Ab 12.

Figure 35 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-390 of the invention, with Figure 35A (SEQ
ID NO:38) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 35B (SEQ ID NO:39) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 35A, Figure 35C (SEQ ID NO:40) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 35D (SEQ
ID NO:41) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 35C.

Figure 36 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-412 of the invention, with Figure 36A (SEQ
ID NO:42) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 36B (SEQ ID NO:43) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 36A, Figure 36C (SEQ ID NO:44) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 36D (SEQ
ID NO:45) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 36C.

Figure 37 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-430/432 of the invention, with Figure 37A
(SEQ ID
NO:46) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 37B (SEQ ID NO:47) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 37A, Figure 37C (SEQ ID NO:48) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 37D (SEQ
ID NO:49) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 37C.

Figure 38 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-467 of the invention, with Figure 38A (SEQ
ID NO:50) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 38B (SEQ ID NO:51) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 38A, Figure 38C (SEQ ID NO:52) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 38D (SEQ
ID NO:53) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 38C.

Figure 39 is a series of representations of the heavy chain and light chain variable region nucleotide and amino acid sequences of the human anti-EPO-R antibody expressed by the cell line designated ABT2-SCX-484 of the invention, with Figure 39A (SEQ
ID NO:54) representing the nucleotide sequence encoding the variable region of the heavy chain, Figure 39B (SEQ ID NO:55) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 39A, Figure 39C (SEQ ID NO:56) representing the nucleotide sequence encoding the variable region of the light chain, and Figure 39D (SEQ
ID NO:57) representing the amino acid sequence encoded by the nucleotide sequence shown in Figure 39C.

Figure 40 is a table showing amino acid sequence alignments of heavy chain variable regions of anti-EPOr mAbs generated according to the invention with their associated germline variable region sequences and identifying framework regions and complementarity determining regions.

Figure 41 is a table showing amino acid sequence alignments of light chain variable regions of anti-EPOr mAbs generated according to the invention with their associated germline variable region sequences and identifying framework regions and complementarity determining regions.

Figure 42 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:86 and SEQ ID NO:87, respectively) and amino acid sequence of the heavy chain of human antibody Ab390. The amino acid sequence comprises SEQ ID
NOS:88 and SEQ ID NOS 72 through 74. The variable chain ends at nucleotide 463. The variable/constant joining region (underlined) is at nucleotides 464-469. The constant region is from nucleotides 470-2006.

Figure 43 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:89 and SEQ ID NO:90, respectively) and amino acid sequence of the light chain of human antibody Ab390. The amino acid sequence comprises SEQ ID
NOS:91. The variable chain ends at nucleotide 463. The variable/constant joining region (underlined) is at nucleotides 464-469. The constant region is from nucleotides 470-718.

Figure 44 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:92 and SEQ ID NO:93, respectively) and amino acid sequence of the heavy chain of human antibody Ab412. The amino acid sequence comprises SEQ ID
NOS:94 and SEQ ID NOS 72 through 74. The variable chain ends at nucleotide 469. The variable/constant joining region (underlined) is at nucleotides 470-475. The constant region is from nucleotides 476-2012.

Figure 45 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:95 and SEQ ID NO:96, respectively) and amino acid sequence of the light chain of human antibody Ab412. The amino acid sequence comprises SEQ ID
NOS:97. The variable chain ends at nucleotide 463. The variable/constant joining region (underlined) is at nucleotides 464-469. The constant region is from nucleotides 470-718.

Figure 46 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:98 and SEQ ID NO:99, respectively) and amino acid sequence of the heavy chain of human antibody Ab432. The amino acid sequence comprises SEQ ID
NOS: 100 and SEQ ID NOS 72 through 74. The variable chain ends at nucleotide 463. The variable/constant joining region (underlined) is at nucleotides 464-469. The constant region is from nucleotides 470-2006.

Figure 47 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:101 and SEQ ID NO:102, respectively) and amino acid sequence of the light chain of human antibody Ab430. The amino acid sequence comprises SEQ ID
NOS:103.
The variable chain ends at nucleotide 463. The variable/constant joining region (underlined) is at nucleotides 464-469. The constant region is from nucleotides 470-718.

Figure 48 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:104 and SEQ ID NO:105, respectively) and amino acid sequence of the heavy chain of human antibody Ab467. The amino acid sequence comprises SEQ ID
NOS:106 and SEQ ID NOS 72 through 74. The variable chain ends at nucleotide 463. The variable/constant joining region (underlined) is at nucleotides 464-469. The constant region is from nucleotides 470-2006.

Figure 49 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:107 and SEQ ID NO:108, respectively) and amino acid sequence of the light chain of human antibody Ab467. The amino acid sequence comprises SEQ ID
NOS:109.
The variable chain ends at nucleotide 463. The variable/constant joining region (underlined) is at nucleotides 464-469. The constant region is from nucleotides 470-718.

Figure 50 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:110 and SEQ ID NO: 111, respectively) and amino acid sequence of the heavy chain of human antibody Ab484. The amino acid sequence comprises SEQ ID
NOS: 112 and SEQ ID NOS 72 through 74. The variable chain ends at nucleotide 469. The variable/constant joining region (underlined) is at nucleotides 470-475. The constant region is from nucleotides 470-2012.' Figure 51 shows the isolated and purified polynucleotide (top strand and bottom strands, SEQ ID NO:113 and SEQ ID NO: 114, respectively) and amino acid sequence of the light chain of human antibody Ab484. The amino acid sequence comprises SEQ ID
NOS: 115.
The variable chain ends at nucleotide 463. The variable/constant joining region (underlined) is at nucleotides 464-469. The constant region is from nucleotides 470-718.

Detailed Description of the Invention Definitions As used herein, the term "antibody" or "immunoglobulin" refers to single chain, two-chain, and multi-chain proteins and glycoproteins that belong to the classes of polyclonal, monoclonal, chimeric and human or humanized. The term "antibody" also includes synthetic and genetically engineered variants thereof.

As used herein, the term "antibody fragment" refers to Fab, Fab', F(ab')2 and Fv fragments, as well as any portion of an antibody having specificity toward at least one desired epitope.
As used herein, the term "gamma-2", "gamma-2 isotype" or "IgG2" refers to subclass 2 of immunoglobulin G (IgG), as well as any antibody fragment thereof. The four subclasses of IgG molecules are well characterized and well known to those of ordinary skill in the art. (See for example, Molecular Biology of the Cell, 2nd Edition by Bruce Alberts et al., 1989) Panels of monoclonal antibodies are available that recognize all human isotypes (IgA,IgG, IgD IgE, and IgM) and subisotypes (IgA1,IgA2, IgGI, IgG2, IgG3, and IgG4) of human immunoglobulins.
As used herein, the term "humanized antibody" refers to an antibody that is derived from a non-human antibody (i.e marine) that retains or substantially retains the antigen-binding properties of the parent antibody but is less immunogenic in humans.

As used herein, the term "human antibody" refers to an antibody that possesses a sequence that is derived from a human germ-line immunoglobulin sequence, such as antibodies derived from transgenic mice having human immunoglobulin genes (e.g., XenoMouse(M mice), human phage display libraries, or human B cells.

As used herein, the term "epitope" refers to any protein determinate capable of specifically binding to an antibody or T-cell receptors. Epitopic determinants usually consist of chemically active surface groupings of molecules such as amino acids or sugar side chains and usually have specific three dimensional structural characteristics, as well as specific charge characteristics.
As used herein, the term "endogenous" refers to a product or activity arising in the body or cell as opposed to a product or activity coming from outside.

As used herein the phrase, a polynucleotide "derived from" or "specific for a designated sequence refers to a polynucleotide sequence that comprises a contiguous sequence of approximately at least 6 nucleotides, preferably at least about 8 nucleotides, more preferably at least about 10-12 nucleotides, and even more preferably at least about 15-20 nucleotides corresponding, i.e., identical or complementary to, a region of the designated nucleotide sequence. The sequence may be complementary or identical to a sequence that is unique to a particular polynucleotide sequence as determined by techniques known in the art. Regions from which sequences may be derived, include but are not limited to, regions encoding specific epitopes, as well as non-translated and/or non-transcribed regions.

The derived polynucleotide will not necessarily be derived physically from the nucleotide sequence of interest under study, but may be generated in any manner, including, but not limited to, chemical synthesis, replication, reverse transcription or transcription, that is based on the information provided by the sequence of bases in the region(s) from which the polynucleotide is derived. As such, it may represent either a sense or an antisense orientation of the original polynucleotide. In addition, combinations of regions corresponding to that of the designated sequence may be modified in ways known in the art to be consistent with the intended use.

As used herein, the phrase "encoded by" refers to a nucleic acid sequence that codes for a polypeptide sequence, wherein the polypeptide sequence or a portion thereof contains an amino acid sequence of at least 3 to 5 amino acids, more preferably at least 8 to 10 amino acids, and even more preferably at least 15 to 20 amino acids from a polypeptide encoded by the nucleic acid sequence. Also encompassed are polypeptide sequences that are immunologically identifiable with a polypeptide encoded by the sequence. Thus, a "polypeptide," "protein" or "amino acid" sequence has at least about 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95% or more identity to the antibodies of the present invention. Further, the antibodies of the present invention may have at least about 60%, 70%, 75%, 80%, 85%, 90%
or 95% similarity to a polypeptide or amino sequences of the antibodies of the present invention. The amino acid sequences of the antibodies of the present invention can be selected from the group consisting of SEQUENCE ID NOS: 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, 39, 41, 43, 45, 47, 49, 51, 53, 55 and 57. Preferred amino acid sequences of the antibodies of the present invention are selected from the group consisting of SEQ ID
NOS: 3, 5, 7, 9, 51 and 53.
As used herein, the phrase "recombinant polypeptide," "recombinant protein,"
or "a polypeptide produced by recombinant techniques", which terms may be used interchangeably herein, describes a polypeptide that by virtue of its origin or manipulation is not associated with all or a portion of the polypeptide with which it is associated in nature and/or is linked to a polypeptide other than that to which it is lined in nature. A recombinant or encoded polypeptide or protein is not necessarily translated from a designated nucleic acid sequence. It also may be generated in any manner, including chemical synthesis or expression of a recombinant expression system.

As used herein, the phrase "synthetic peptide" refers to a polymeric form of amino acids of any length, which may be chemically synthesized by methods well known in the art (See U.S. Patents 4,816,513, 5,854,389, 5,891,993 and 6,184,344).
As used herein, the term "polynucleotide" refers to a polymeric form of nucleotides of any length, either ribonucleotides or deoxyribonucleotides. This term refers only to the primary structure of the molecule. Thus, the term includes double and single-stranded DNA as well as double- and single-stranded RNA. It also includes modifications, such as methylation or capping and unmodified forms of the polynucleotide. The terms "polynucleotide", "oligomer," "oligonucleotide," and "oligo," are used interchangeably herein.

As used herein the phrase "purified polynucleotide" refers to a polynucleotide of interest or fragment thereof that is essentially free, e.g. contains less than about 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95% of the protein with which the polynucleotide is naturally associated. Techniques for purifying polynucleotides of interest are well known in the art and include, for example, disruption of the cell containing the polynucleotide with a chaotropic agent and separation of the polynucleotide(s) and proteins by ion-exchange chromatography, affinity chromatography and sedimentation according to density.
As used herein, the phrase "purified polypeptide" or "purified protein" means a polypeptide of interest or fragment thereof which is essentially free of, e.g., contains less than about 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95%, cellular components with which the polypeptide of interest is naturally associated. Methods for purifying polypeptides of interest are known in the art.

As used herein, the term "isolated" refers to material that is removed from its original environment (e.g., the natural environment if it is naturally occurring). For example, a naturally occurring polynucleotide or polypeptide present in a living animal is not isolated, but the same polynucleotide or DNA or polypeptide, separated from some or all of the coexisting materials in the natural system, is isolated. Such polynucleotide could be part of a vector and/or such polynucleotide or polypeptide could be part of a composition, and still be isolated in that the vector or composition is not part of its natural environment.

As used herein, the term "polypeptide" and "protein" are used interchangeably and refer to at least one molecular chain of amino acids linked through covalent and/or non-covalent bonds. The terms do not refer to a specific length of the product.
Thus, peptides, oligopeptides and proteins are included within the definition of polypeptide.
The terms include post-translational modifications of the polypeptide, including, but not limited to, glycosylations, acetylations, phosphorylations and the like. In addition, protein fragments, analogs, mutated or variant proteins, fusion proteins and the like are included within the meaning of polypeptide.
As used herein, the phrase "recombinant host cells," "host cells," "cells,"
"cell lines,"
"cell cultures," and other such terms denoting microorganisms or higher eukaryotic cell lines cultured as unicellular entities refer to cells that can be, or have been, used as recipients for recombinant vector or other transferred DNA, and include the original progeny of the original cell that has been transfected.

As used herein, the term "replicon" refers to any genetic element, such as a plasmid, a chromosome or a virus, that behaves as an autonomous unit of polynucleotide replication within a cell.
As used herein, the term "operably linked" refers to a situation wherein the components described are in a relationship permitting them to function in their intended manner. Thus, for example, a control sequence "operably linked" to a coding sequence is ligated in such a manner that expression of the coding sequence is achieved under conditions compatible with the control sequence.

As used herein, the term "vector" refers to a replicon in which another polynucleotide segment is attached, such as to bring about the replication and/or expression of the attached segment.
As used herein, the term "control sequence" refers to a polynucleotide sequence that is necessary to effect the expression of a coding sequence to which it is ligated. The nature of such control sequences differs depending upon the host organism. In prokaryotes, such control sequences generally include a promoter, a ribosomal binding site and terminators and, in some instances, enhancers. The term "control sequence" thus is intended to include at a minimum all components whose presence is necessary for expression, and also may include additional components whose presence is advantageous, for example, leader sequences.
The term "transfection" refers to the introduction of an exogenous polynucleotide into a prokaryotic or eucaryotic host cell, irrespective of the method used for the introduction. The term "transfection" refers to both stable and transient introduction of the polynucleotide, and encompasses direct uptake of polynucleotides, transformation, transduction and f-mating. -Once introduced into the host cell, the exogenous polynucleotide may be maintained as a non-integrated replicon, for example, a plasmid, or alternatively, may be integrated into the host genome.

As used herein, the term "treatment" refers to prophylaxis and/or therapy.
As used herein, the term "purified product" refers to a preparation of the product which has been isolated from the cellular constituents with which the product is normally associated and from other types of cells that may be present in the sample of interest.

As used herein, the phrase "activation of an erythropoietin (EPO) receptor"
refers to one or more molecular processes which an EPO receptor undergoes that result in the transduction of a signal to the interior of a receptor-bearing cell.
Ultimately, this signal brings about one or more changes in cellular physiology. Activation of the EPO
receptor typically results in the proliferation or differentiation of EPO receptor-bearing cells, such as, but not limited to, erythroid progenitor cells. A number of events are involved in the activation of the EPO receptor, such as, but not limited to, the dimerization of the receptor.

The structural unit of an antibody is a tetramer. Each tetramer is composed of two identical pairs of polypeptide chains, each pair having one "light" (25 kDa) and one "heavy"
chain (about 50-70 kDa). The amino-terminal portion of each chain includes a variable region that is primarily responsible for antigen recognition. The carboxy-terminal portion of the chain defines a constant region that is responsible for the effector function of the antibody. Human light chains are classified as kappa and lambda light chains. Heavy chains are classified as mu, delta, gamma, alpha, or epsilon and define the antibody's isotype as IgM, IgD, IgG, IgA, and IgE. IgG immunoglobulins are classified further into four subclasses (IgGi, IgG2, IgG3 and IgG4) having gamma-1, gamma-2, gamma-3 and gamma-4 heavy chains, respectively.
Most of the therapeutic human, chimeric or humanized antibodies available are of the IgGi antibody type including Herceptin for breast cancer, Rituxan for Non-Hodgkins lymphoma and Humira and Remicade for rheumatoid arthritis (See Glennie, M.J. et al., Drug Discovery Today, 8:503 (2003).

Within the light and heavy chains, the variable and constant regions are joined by a "J"
region with the heavy chain also include a "D" region. The variable regions of each light/heavy chain pair form the antigen binding site. Thereupon, an intact antibody has two binding sites, which, except in bifunctional or bispecific antibodies, are the same. Bifunctional or bispecific antibodies are artificial hybrid antibodies that have two different heavy/light chain pairs and two different binding sites. Bifunctional or bispecific antibodies can be produced using routine techniques known in the art.

The structure of the chains of an antibody exhibit the same general structure of relatively conserved framework regions (FR) joined by three hyper variable regions, also called complementarity determining regions or CDRs. The CDRs from the two chains of each pair are aligned by the framework regions, enabling binding to a specific epitope. From N-terminal to C-terminal, both the light and heavy chains comprise the domains FR1, CDR1, FR2, CDR2, FR3, CDR3 and FR4.

U.S. Patent 6,319,499 describes antibodies that bind to and activate an erythropoietin receptor (EPO-R). The antibodies specifically identified in this patent are Mabs 71 and 73.
Mab 71 binds to a peptide designated "SE-3" having the amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV (SEQ ID NO:1) (See Example 3). SE-3 is located on the human EPO-R between amino acid residues 49-78. According to U.S. Patent 6,319,499, when this region of the EPO-R (i.e. amino acid residues 49-79) is bound with a cross linker such as Mab 71, this results in the activation of the EPO
receptor. Example 6 in U.S. Patent 6,319,499 states that Mab 71 binds "significant amounts of peptide SE-3"
compared to other peptides tested. This example further states that this "indicates that Mab 71 binds to a region of the human EPO-R containing or overlapping residues 49 to 78." Mabs 71 and 73 are murine antibodies. Although rodent and human antibodies may both provide precision for target specificity, human antibodies interact far more effectively with the natural defenses of the body and do not elicit anti-antibody responses to the same extent as rodent antibodies (Winter, G. and Milstein, C. Nature 349: 293 (1991). Additionally, the flexibility of human IgG subclasses differ (Roux, K.H. et al., J. Immunol. 159: 3372 (1997) and this difference also extends to rodent IgG isotypes since rodent IgG isotypes differ from their human counterparts. Since protein flexibility may affect antibody-antigen recognition (Jimenez, R., et al. Proc. Natl. Acad Sci. USA, 100: 92 (2003), human IgG2 isotypes may result in antigen recognition mechanisms distinct from those of murine antibodies. Murine IgG
isotypes generally differ from those of humans.

In one embodiment, the present invention relates to an antibody or antibody fragment that binds to the erythropoietin receptor. The antibody or antibody fragment that binds to the erythropoietin receptor comprises at least one heavy chain having an amino acid sequence selected from the group consisting of. SEQ ID NOS: 3, 7, 11, 15, 19, 31, 35, 39, 43, 47, 51, 55 and fragments thereof. In a second embodiment, the antibody or antibody fragment that binds to the erythropoietin receptor comprises at least one light chain having an amino acid sequence selected from the group consisting of. SEQ ID NOS: 5, 9, 13, 17, 21, 23, 25, 27, 29, 33, 37, 41, 45, 49, 53, 57 and fragments thereof.
In a third embodiment, the present invention relates to an isolated antibody that is capable of binding a human erythropoietin receptor in a mammal. More specifically, the antibody comprises a heavy chain variable region or a light chain variable region which comprises a continuous sequence from CDR1 through CDR3. The amino acid sequence of the heavy chain variable region comprising the continuous sequence from CDR1 through CDR3 is selected from the group consisting of. SEQ ID NO:58, SEQ ID NO:59,, SEQ ID
NO:60 and SEQ ID NO:61, and fragments thereof. The amino acid sequence of the light chain variable region comprising the continuous sequence from CDR1 through CDR3 is selected from the group consisting of. SEQ ID NO:62, SEQ ID NO:63, SEQ ID NO:64, SEQ ID NO:65, SEQ
ID NO:66, SEQ ID NO:67, and SEQ ID NO:68, and fragments thereof. In addition, the present invention relates to an isolated antibody which comprises a heavy chain variable region or a light chain variable region which comprises at least one CDR. More specifically, the antibody comprises a heavy chain variable region comprising at least one CDR
selected from the group consisting of amino acid residues 99-112 of SEQ ID NO: 11, 26-35 of SEQ ID NO:3, 50-65 of SEQ ID NO:3, 98-105 of SEQ ID NO:3, 26-35 of SEQ ID NO:19, 50-66 of SEQ ID
NO:19, 99-105 of SEQ ID NO:19, 50-66 of SEQ ID NO:31, 99-105 of SEQ ID NO:31, of SEQ ID NO:39, 50-65 of SEQ ID NO:39, 98-105 of SEQ ID NO:39, 26-37 of SEQ
ID
NO:43, 52-67 of SEQ ID NO:43, 100-107 of SEQ ID NO:43, 26-35 of SEQ ID NO:47, of SEQ ID NO:47, 26-35 of SEQ ID NO:51, 50-65 of SEQ ID NO:51, 98-105 of SEQ
ID
NO:51, 26-37 of SEQ ID NO:55 and 52-67 of SEQ ID NO:55 or a light chain variable region comprising at least one CDR selected from the group consisting of amino acid residues 24-34 of SEQ ID NO:13, 50-56 of SEQ ID NO:13, 89-97 of SEQ ID NO:5, 24-34 of SEQ ID
NO:27, 50-56 of SEQ ID NO:9, 24-39 of SEQ ID NO:33, 55-61 of SEQ ID NO:33, 24-34 of SEQ ID
NO:41, 89-97 of SEQ ID NO:41, 24-34 of SEQ ID NO:45, 50-56 of SEQ ID NO:45, 89-97 of SEQ ID NO:45, 89-97 of SEQ ID NO:49 and 24-34 of SEQ ID NO:57.

In a fourth embodiment, the present invention relates to an antibody or antibody fragment that binds to and activates the erythropoietin receptor. The antibodies of the present invention bind to at least one epitope that is involved in activating the EPO
receptor (Example 4). Unlike other antibodies or fragments known in the art that bind to and activate an erythropoietin receptor, such as the antibodies described in U.S. Patent 6,319,499, the antibodies of the present invention do not interact with the peptide designated SE-3.
Surprisingly, the antibodies of the present invention are erythropoietic even though the antibodies do not bind to the SE-3 peptide. Therefore, the human antibodies of the present invention interact with at least one different epitope on the human EPO
receptor than the antibodies described in U.S. Patent 6,319,499.

In a fifth embodiment, the present invention relates to an IgG2 antibody or antibody fragment that binds to and activates the erythropoietin receptor. The IgG2 antibodies or antibody fragments of this embodiment bind to and interact with any epitope that is involved in activating the EPO receptor.

Additionally, as demonstrated by the BlAcore results shown in Example 1, the antibodies of the present invention exhibit a binding affinity to the erythropoietin receptor within one hundred fold of the binding affinity of endogenous human erythropoietin to the erythropoietin receptor. A high (-InM) and low (-l M) affinity of the EPO
receptor for EPO

has been reported resulting from two nonequivalent receptor binding sites on EPO (See Philo, J.S. et al., Biochemistry, 35:1681 (1996)).

The antibodies of the present invention can be polyclonal antibodies, monoclonal antibodies, chimeric antibodies (See U.S. Patent 6,020,153) or human or humanized antibodies or antibody fragments thereof. Synthetic and genetically engineered variants (See U.S. Patent 6,331,415) of any of the foregoing are also contemplated by the present invention. Preferably, however, the antibodies of the present invention are human or humanized antibodies. The advantage of human or humanized antibodies is that they potentially decrease or eliminate the immunogenicity of the antibody in a host recipient, thereby permitting an increase in the bioavailability and a reduction in the possibility of adverse immune reaction, thus potentially enabling multiple antibody administrations.

Humanized antibodies include chimeric or CDR-grafted antibodies. Also, human antibodies can be produced using genetically engineered strains of animals in which the antibody gene expression of the animal is suppressed and functionally replaced with human antibody gene expression.

Methods for making humanized and human antibodies are known in the art. One method for making human antibodies employs the use of transgenic animals, such as a transgenic mouse. These transgenic animals contain a substantial portion of the human antibody producing genome inserted into their own genome and the animal's own endogenous antibody production is rendered deficient in the production of antibodies.
Methods for making such transgenic animals are known in the art. Such transgenic animals can be made using XenoMouse technology or by using a "minilocus" approach. Methods for making XenomiceTM are described in U.S. Patent Nos. 6,162,963, 6,150,584, 6,114,598 and 6,075,181.
Methods for making transgenic animals using the "minilocus" approach are described in U.S.
Patents 5,545,807, 5,545,806 and 5,625,825. Also see International Publication No.
W093/12227.
Using the XenoMouse technology, human antibodies can be obtained by immunizing a XenoMouse mouse (Abgenix, Fremont, California) with an antigen of interest.
The lymphatic cells (such as B-cells) are recovered from the mice that express antibodies. These recovered cells can be fused with myeloid-type cell line to prepare immortal hybridoma cell lines. These hybridoma cell lines can be screened and selected to identify hybridoma cell lines that produce antibodies specific to the antigen of interest. Alternatively, the antibodies can be expressed in cell lines other than hybridoma cell lines. More specifically, sequences encoding particular antibodies can be cloned from cells producing the antibodies and used for transformation of a suitable mammalian host cell.

Transformation can be by any known method for introducing polynucleotides into a host cell, including, for example, packaging the polynucleotide in a virus or into a viral vector and transducing a host cell with a virus or vector or by transfection procedures known in the art such as those described in U.S. Patents 4,399,216, 4,912,040, 4,740,461 and 4,959,455. For example, one or more genes encoding the heavy chain can be expressed in a cell and one or more genes encoding the light chain can be expressed in a second cell. The resulting heavy and light chains can then be fused together to form the antibodies of the present invention using techniques known in the art. Alternatively, genes encoding for parts of the heavy and light chains can be ligated using restriction endonucleases to reconstruct the gene coding for each chain. Such a gene can then be expressed in a cell to produce the antibodies of the present invention.

The transformation procedure used will depend upon the host to be transformed.
Methods for introducing heterologous polynucleotides into mammalian cells are well known in the art and include dextran-mediated transfection, calcium phosphate precipitation, polybrene mediated transfection, protoplast fusion, electroporation, encapsulation of the polynucleotide(s) into liposomes and direct microinjection of the DNA
molecule.

Mammalian cell lines that can be used as hosts for expression are well known in the art and include, but are not limited to, Chinese hamster ovary (CHO) cells, HeLa cells, baby hamster kidney (BHK) cells, monkey kidney cells (COS), human hepatocellular carcinoma cells bacterial cells, such as E. coli, yeast cells, such as Saccharomyces cerevisiae, etc.
Humanized antibodies can also be made using a CDR-grafted approach. Such humanized antibodies are well known in the art. Generally, humanized antibodies are produced by obtaining nucleic acid sequences that encode the variable heavy and variable light sequences of an antibody that binds to the EPO receptor, identifying the complementary determining region or "CDR" in the variable heavy and variable light sequences and grafting the CDR nucleic acid sequences on to human framework nucleic acid sequences.
(See, for example, U.S. Patent Nos. 4,816,567 and 5,225,539).
The human framework that is selected is one that is suitable for in vivo administration, meaning that it does not exhibit immunogenicity. For example, such a determination can be made by prior experience with in vivo usage of such antibodies and studies of amino acid similarities.
Methods for cloning nucleic acids are known in the art. These methods involve amplification of the antibody sequences to be cloned using appropriate primers by polymerase chain reaction (PCR). Primers that are suitable for amplifying antibody nucleic acid sequences and specifically murine variable heavy and variable light sequences are known in the art.
Once the CDRs and FRs of the cloned antibody sequences that are to be humanized are identified, the amino acid sequences encoding the CDRs are identified and the corresponding nucleic acid sequences grafted on to selected human FRs. This can be done using known primers and linkers, the selection of which are known in the art.
After the CDRs are grafted onto selected human FRs, the resulting "humanized"
variable heavy and variable light sequences are expressed to produce a humanized Fv or humanized antibody that binds to the EPO receptor. Typically, the humanized variable heavy and light sequences are expressed as a fusion protein with human constant domain sequences so an intact antibody that binds to the EPO receptor is obtained. However, a humanized Fv antibody can be produced that does not contain the constant sequences. Fusion of the human constant sequence to the humanized variable region is preferred.

The EPO receptor that is bound by and preferably activated using the antibodies of the present invention is preferably a mammalian EPO receptor, most preferably a human EPO
receptor. The present invention also contemplates the use of analogs of the EPO receptor, such as those described in U.S. Patent 5,292,654. Human EPO receptor can be purchased from R &
D Systems (Minneapolis, Minnesota).

An example of two (2) antibodies that (1) bind to and activate the EPO
receptor; (2) do not interact with a peptide having an amino acid sequence of PGNYSFSYQLEDEPWKLCRLHQAPTARGAV (SEQ ID NO: 1); and (3) exhibit a binding affinity within one hundred fold of the binding affinity of endogeous human EPO to the EPO
receptor, are the human antibodies designated Ab12 and Ab198. Ab12 and Ab198 are human antibodies that were developed using the XenoMouse XenoMax technology described herein (See Example 1).

In another embodiment, the present invention relates to polynucleotide and polypeptide sequences that encode for the antibodies described herein. Preferably, such polynucleotides encode for both the variable and constant regions of each of the heavy and light chains, although other combinations are also contemplated by the present invention.

The present invention also contemplates oligonucleotide fragments derived from the disclosed polynucleotides and nucleic acid sequences complementary to these polynucleotides.
The polynucleotides can be in the form of RNA or DNA. Polynucleotides in the form of DNA, cDNA, genomic DNA, nucleic acid analogs and synthetic DNA are within the scope of the present invention. The DNA may be double-stranded or single-stranded, and if single stranded, may be the coding (sense) strand or non-coding (anti-sense) strand.
The coding sequence that encodes the polypeptide may be identical to the coding sequence provided herein or may be a different coding sequence which coding sequence, as a result of the redundancy or degeneracy of the genetic code, encodes the same polypeptide as the DNA
provided herein.

Preferably, the polynucleotides encode at least one heavy chain variable region and at least one light chain variable region of the present invention. Examples of such polynucleotides are shown in SEQ ID NOS: 2, 4, 6, 8, 10, 12, 14,16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54 and 56 as well as fragments, complements and degenerate codon equivalents thereof. For example, SEQ ID NO: 2 encodes for the heavy chain of Ab12 (variable region) and SEQ ID NO:4 encodes for the light chain of Ab12 (variable region). SEQ ID NO:6 encodes for the heavy chain of Ab198 (variable region) and SEQ ID NO: 8 encodes for the light chain of Ab 198 (variable region).

The present invention also includes variant polynucleotides containing modifications such as polynucleotide deletions, substitutions or additions, and any polypeptide modification resulting from the variant polynucleotide sequence. A polynucleotide of the present invention may also have a coding sequence that is a naturally occurring variant of the coding sequence provided herein.

It is contemplated that polynucleotides will be considered to hybridize to the sequences provided herein if there is at least 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95%
identity between the polynucleotide and the sequence.
The present invention further relates to polypeptides that encode for the antibodies of the present invention as well as fragments, analogs and derivatives of such polypeptides. The polypeptides of the present invention may be recombinant polypeptides, naturally purified polypeptides or synthetic polypeptides. The fragment, derivative or analogs of the polypeptides of the present invention may be one in which one or more of the amino acid residues is substituted with a conserved or non-conserved amino acid residue (preferably a conserved amino acid residue) and such substituted amino acid residue may or may not be one encoded by the genetic code; or it may be one in which one or more of the amino acid residues includes a substituent group; or it may be on in which the polypeptide is fused with another compound, such as a compound to increase the half-life of the polypeptide (for example, polyethylene glycol); or it may be one in which the additional amino acids are fused to the polypeptide, such as a leader or secretory sequence or a sequence that is employed for purification of the polypeptide or a proprotein sequence. Such fragments, derivatives and analogs are within the scope of the present invention.
A polypeptide of the present invention may have an amino acid sequence that is identical to that of the antibodies described herein or that is different by minor variations due to one or more amino acid substitutions. The variation may be a "conservative change" typically in the range of about 1 to 5 amino acids, wherein the substituted amino acid has similar structural or chemical properties, e.g., replacement of leucine with isoleucine or threonine with serine. In contrast, variations may include nonconservative changes, e.g., replacement of a glycine with a tryptophan. Similar minor variations may also include amino acid deletions or insertions or both. Guidance in determining which and how many amino acid residues may be substituted, inserted, or deleted without changing biological or immunological activity may be found using computer programs well known in the art, for example DNASTAR
software (DNASTAR, Inc., Madison, Wisconsin).

Preferably, the polypeptides encode at least one heavy chain variable region or at least one light chain variable region of the antibodies of the present invention.
More preferably, the polypeptides encode at least one heavy chain variable region and one light chain variable region of the antibodies of the present invention. Examples of such polypeptides are those having the amino acid sequences shown in SEQ ID NOS: 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37, 39, 41, 43, 45, 46, 47, 49, 51, 53, 55, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, and fragments thereof. Specifically, the heavy chain of Ab12 has the amino acid sequence shown in SEQ ID NO: 3 and the light chain has the amino acid sequence shown in SEQ ID NO:5. The amino acid sequence of the heavy chain of Ab198 is shown in SEQ ID
NO:7 and the light chain has the amino acid sequence shown in SEQ ID NO:9.

The present invention also provides vectors that include the polynucleotides of the present invention, host cells which are genetically engineered with vectors of the present invention and the production of the antibodies of the present invention by recombinant techniques.

Host cells are genetically engineered (transfected, transduced or transformed) with vectors, such as, cloning vectors or expression vectors. The vector may be in the form of a plasmid, a viral particle, a phage, etc. The engineered host cells can be cultured in conventional nutrient media modified as appropriate for activating promoters, selecting transfected cells, etc. The culture conditions, such as temperature, pH and the like, are those previously used with the host cell selected for expression, and will be apparent to those of skilled in the art.

The polynucleotides of the present invention can be employed to produce the polypeptides and hence the antibodies of the present invention. The polynucleotide sequences of the present invention can be included in any one of a variety of expression vehicles, in particular, vectors or plasmids for expressing a polypeptide. Such vectors include chromosomal, nonchromosomal and synthetic DNA sequences, derivatives of SV40, bacterial plasmids, phage DNA, yeast plasmids, vectors derived from combinations of plasmids and phage DNA, viral DNA such as vaccinia, adenovirus, fowl pox virus and pseudorabies.
However, any other plasmid or vector may be used so long as it is replicable and viable in the host.
The appropriate DNA sequence may be inserted into the vector by a variety of procedures. In general, the DNA sequence is inserted into appropriate restriction endonuclease sites by procedures known in the art. The polynucleotide sequence in the expression vector is operatively linked to an appropriate expression control sequence (i.e.
promoter) to direct mRNA synthesis. Examples of such promoters include, but are not limited to, the LTR or the SV40 promoter, the E. coli lac or trp, the phage lambda PL promoter and other promoters known to control expression of genes in prokaryotic or eukaryotic cells or their viruses. The expression vector also contains a ribosome binding site for translation initiation and a transcription terminator. The vector may also include appropriate sequences for amplifying expression. For example, the vector can contain enhancers, which are transcription-stimulating DNA sequences of viral origin, such as those derived form simian virus such as SV40, polyoma virus, bovine papilloma virus or Moloney sarcoma virus, or genomic, origin. The vector preferably also contains an origin of replication. The vector can be constructed to contain an exogenous origin of replication or, such an origin of replication can be derived from SV40 or another viral source, or by the host cell chromosomal replication mechanism.

In addition, the vectors preferably contain a marker gene for selection of transfected host cells such as dihydrofolate reductase or antibiotics, such as G-418 (geneticin, a neomycin-derivative) or hygromycin, or genes which complement a genetic lesion of the host cells such as the absence of thymidine kinase, hypoxanthine phosphoribosyl transferase, dihydrofolate reductase, etc.

Suitable vectors for use in the present invention are known in the art. Any plasmid or vector can be used in the present invention as long as it is replicable and is viable in the host.
Examples of vectors that can be used include those that are suitable for mammalian hosts and based on viral replication systems, such as simian virus 40 (SV40), Rous sarcoma virus (RSV), adenovirus 2, bovine papilloma virus (BPV), papovavirus BK mutant (BKV), or mouse and human cytomegalovirus (CVM).

In a further embodiment, the present invention relates to host cells containing the above-described constructs. The host cell can be a higher eukaryotic cell, such as a mammalian cell, or a lower eukaryotic cell, such as a yeast cell, or the host cell can be a prokaryotic cell, such as a bacterial cell. Preferably, the host cells provide a suitable environment for the production of active antibodies, since the biosynthesis of functional tetrameric antibody molecules requires correct nascent polypeptide chain folding, glycosylation, and assembly. Example of suitable host cells, include mammalian cells, such as COS-7 cells, Bowes melanoma cells, Chinese hamster ovary (CHO) cells, embryonic lung cells L-132, and mammalian cells of lymphoid origin, such as myeloma or lymphoma cells.
The host cells can be transfected with a vector containing a polynucleotide sequence encoding the H-chain alone, with a second vector encoding the light chain alone (such as by using two different vectors as discussed previously). Preferably, the host cells are transfected with two different vectors.
Introduction of the vectors into the host cell can be effected by calcium phosphate transfection, DEAE-Dextran mediated transfection or electroporation (L. David et al., Basic Methods in Molecular Biology 2nd Edition, Appleton and Lang, Paramount Publishing, East Norwalk, Conn. (1994)).
In order to obtain the antibodies of the present invention, one or more polynucleotide sequences that encode for the light and heavy chain variable regions and light and heavy chain constant regions of the antibodies of the present invention should be incorporated into a vector.
Polynucleotide sequences encoding the light and heavy chains of the antibodies of the present invention can be incorporated into one or multiple vectors and then incorporated into the host cells.

Cell lines expressing Ab12 and Ab467 antibodies were deposited with the American Type Culture Collection (ATCC), 10801 University Boulevard, Manassas, Virginia 20110, under the terms of the Budapest Treaty, on September 30, 2003 and were accorded accession numbers PTA-5554 and PTA-5555. These deposits are provided for the convenience of those skilled in the art and are neither an admission that such deposits are required to practice the invention nor that equivalent embodiments are not within the skill of the art in view of the present disclosure. The public availability of these deposits is not a grant of a license to make, use or sell the deposited materials under this or any other patents. The nucleic acid sequences of the deposited materials are controlling if in conflict with any sequence described herein.
The antibodies of the present invention have a number of uses. In general, the antibodies may be used to treat any condition treatable by erythropoietin or a biologically active variant or analog thereof. For example, antibodies of the invention are useful for treating disorders characterized by low red blood cell levels and/or decreased hemoglobin levels (e.g. anemia). In addition, the antibodies of the invention may be used for treating disorders characterized by decreased or subnormal levels of oxygen in the blood or tissue, such as, for example, hypoxemia or chronic tissue hypoxia and/or diseases characterized by inadequate blood circulation or reduced blood flow. Antibodies of the invention also may, be useful in promoting wound healing or for protecting against neural cell and/or tissue damage, resulting from brain/spinal cord injury, stroke and the like. Non-limiting examples of conditions that may be treatable by the antibodies of the invention include anemia, such as chemotherapy-induced anemia, cancer associated anemia, anemia of chronic disease, HIV-associated anemia, bone marrow transplant-associated anemia and the like, heart failure, ischemic heart disease and renal failure. As such, the invention includes methods of treating any of the aforementioned diseases or conditions comprising the step of administering to a mammal a therapeutically effective amount of said antibody. Preferably, the mammal is a human.

The antibodies of the present invention also can be used to identify and diagnose mammals that have a dysfunctional EPO receptor. Mammals that have a dysfunctional EPO
receptor are characterized by disorders such as anemia. Preferably, the mammal being identified and diagnosed is a human. Additionally, the antibodies of the present invention can be used in the treatment of anemia in mammals suffering from red blood cell aplasia. Red blood cell aplasia may result from the formation of neutralizing anti-erythropoietin antibodies in patients during treatment with recombinant erythropoietin (Casadevall, N.
et al., n. Eng. J.
Med. 346: 469 (2002)). The method involves the step of administering to a mammal suffering from said aplasia and in need of treatment a therapeutically effective amount of the antibodies of the present invention.

In another embodiment of the invention, the EPO receptor antibodies and antibody fragments of the invention also can be used to detect EPO receptor (e.g., in a biological sample, such as tissue specimens, intact cells, or extracts thereof), using a conventional immunoassay, such as an enzyme linked immunosorbent assay (ELISA), a radioimmunoassay (RIA) or tissue immunohistochemistry. The invention provides a method for detecting EPO
receptor in a biological sample comprising contacting a biological sample with an antibody or antibody fragment of the invention and detecting either the antibody (or antibody portion), to thereby detect EPO receptor in the biological sample. The antibody or antibody fragment is directly or indirectly labeled with a detectable substance to facilitate detection of the bound or unbound antibody or antibody fragment. A variety of immunoassay formats may be practiced (such as competitive assays, direct or indirect sandwich immunoassays and the like) and are well known to those of ordinary skill in the art.

Suitable detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials and radioactive materials. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, B-galactosidase, or acetylcholinesterase;
examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin;
examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine, dansyl chloride or phycoerythrin; and an example of a luminescent material includes luminol; and examples of suitable radioactive material include 1251, 131I335S. or 3H.

In yet another embodiment, the present invention relates to a pharmaceutical composition containing a therapeutically effective amount of the antibody of the present invention along with a pharmaceutically acceptable carrier or excipient. As used herein, "pharmaceutically acceptable carrier" or "pharmaceutically acceptable excipient" includes any and all solvents, dispersion media, coating, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible.
Examples of pharmaceutically acceptable carriers or excipients include one or more of water, saline, phosphate buffered saline, dextrose, glycerol, ethanol and the like as well as combinations thereof. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as mannitol, sorbitol, or sodium chloride in the composition.
Pharmaceutically acceptable substances such as wetting or minor amounts of auxiliary substances such as wetting or emulsifying agents, preservatives or buffers, which enhance the shelf life or effectiveness of the of the antibody or antibody portion also may be included.
Optionally, disintegrating agents can be included, such as cross-linked polyvinyl pyrrolidone, agar, alginic acid or a salt thereof, such as sodium alginate and the like. In addition to the excipients, the pharmaceutical composition can include one or more of the following, carrier proteins such as serum albumin, buffers, binding agents, sweeteners and other flavoring agents;
coloring agents and polyethylene glycol.

The compositions of this invention may be in a variety of forms. They include, for example, liquid, semi-solid and solid dosage forms, such as liquid solutions (e.g. injectable and infusible solutions), dispersions or suspensions, tablets, pills, powders, liposomes and suppositories. The preferred form depends on the intended mode of administration and therapeutic application. Typical preferred compositions are in the form of injectable or infusible solutions, such as compositions similar to those used for passive immunization of humans with other antibodies. The preferred mode of administration is parenteral (e.g., intravenous, subcutaneous, intraperitoneal, intramuscular). In a preferred embodiment, the antibody is administered by intravenous infusion or injection. In another preferred embodiment, the antibody or antibody fragment is administered by intramuscular or subcutaneous injection.
Other suitable routes of administration for the pharmaceutical composition include, but are not limited to, rectal, transdermal, vaginal, transmucosal or intestinal administration.
Therapeutic compositions typically must be sterile and stable under the conditions of manufacture and storage. The composition can be formulated as a solution, microemulsion, dispersion, liposome, or other ordered structure suitable to high drug concentration. Sterile injectable solutions can be prepared by incorporating the active compound (i.e. antibody or antibody fragment) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle that contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying that yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof. The proper fluidity of a solution can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prolonged absorption of injectable compositions can be brought about by including in the composition an agent that delays absorption, for example, monostearate salts and gelatin.

The antibodies and antibody fragments of the invention can be administered by a variety of methods known in the art, although for many therapeutic applications, the preferred route/mode of administration is intravenous injection or infusion. As will be appreciated by the skilled artisan, the route and/or mode of administration will vary depending upon the desired results. In certain embodiments, the active compound may be prepared with a carrier that will protect the compound against rapid release, such as a controlled release formulation, including implants, transdermal patches, and microencapsulated delivery systems.
Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Many methods for the preparation of such formulations are patented or generally known to those skilledin the art. See, e.g. Sustained and Controlled Release Drug Delivery Systems, J. R.
Robinson, ed., Marcel Dekker, Inc., New York, 1978).

In certain embodiments, an antibody or antibody portion of the invention may be orally administered, for example, with an inert diluent or an assimilable edible carrier. The compound (and other ingredients if desired) may also be enclosed in a hard or soft shell gelatin capsule, compressed into tablets, buccal tablets, troches, capsules, elixiers, suspensions, syrups, wafers, and the like. To administer an antibody or antibody fragment of the invention by other than parenteral administration, it may be necessary to coat the compound with, or co-administer the compound with, a material to prevent its inactivation.

Supplementary active compounds also can be incorporated into the compositions.
In certain embodiments, an antibody or antibody fragment of the invention is coformulated with and/or coadministered with one or more additional therapeutic agents. For example, an EPO

receptor antibody or antibody fragment of the invention may be coformulated and/or coadministerd with one or more additional antibodies that bind other targets (e.g. , antibodies that bind other cytokines or that bind cell surface molecules) or one or more cytokines.
Furthermore, one or more antibodies of the invention may be used in combination with two or more of the foregoing therapeutic agents. Such combination therapies may advantageously utilize lower dosages of the administered therapeutic agents, thus avoiding possible toxicities or complications associated with the various monotherapies.

As used herein, the term "therapeutically effective amount" means an amount of antibody or antibody fragment that produces the effects for which it is administered. The exact dose will be ascertainable by one skilled in the art. As known in the art, adjustments based on age, body weight, sex, diet, time of administration, drug interaction and severity of condition may be necessary and will be ascertainable with routine experimentation by those skilled in the art. A therapeutically effective amount is also one in which the therapeutically beneficial effects outweigh any toxic or detrimental effects of the antibody or antibody fragment. A
"prophylactically effective amount" refers to an amount effective, at dosages and for periods of time necessary to achieve the desired prophylactic result. Typically, since a prophylactic dose is used in subjects prior to or at an earlier stage of disease, the prophylactically effective amount will be less than the therapeutically effective amount.
Dosage regimens may be adjusted to provide the optimum desired response (e.g., a therapeutic or prophylactic response). For example, a single bolus may be administered, several divided doses may be administered over time or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation. It is especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the mammalian subjects to be tested; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
The specification for the dosage unit forms of the invention are dictated by and directly dependent on (a) the unique characteristics of the active compound and the particular therapeutic or prophylactic effect to be achieved and (b) the limitations inherent in the art of compounding such an active compound for the treatment of sensitivity in individuals.

An exemplary, non-limiting range for a therapeutically or prophylactically effective amount of an antibody or antibody portion of the invention is 0.1-20 mg/kg, more preferably 1-mg/kg. It is to be noted that dosage values may vary with the type and severity of the 5 condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that dosage ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition.
By way of example, and not of limitation, examples of the present invention shall now be given.

EXAMPLE 1: Generation of human Erythropoietin Receptor antibodies Antigen Preparation. The antigen used for immunization of XenoMouse animals was coupled to a universal T-cell epitope (TCE) (Jlmmunol., 148(5):1499 (1992)) using two different methods. A mixture containing an equal amount of each was used as the immunogen.

1) 2.3 mg of Dithiothreitol (DTT), and 200 mcg of cysteine coupled TCE
(J.Immunol., 148(5):1499 (1992)) are mixed at room temperature for 30 minutes. DTT is removed by centrifugation through a SephadexMG10 (Pharmacia, Upsala, Sweden) chromatography column.
The reduced cysteine coupled TCE is added to 200 mcg soluble extracellular domain of human EpoR (R&D Systems, Minneapolis, MN) re-suspended in Phosphate Buffered Saline (PBS) (8.1 mM Na2HP04, 1.6 mM NaH2PO4i 136 mM NaCl, 2.6 mM KCI, pH 7.4) and 33 mcg of Sulfosuccinimidyl 4-(N-maleimidomethyl)-cyclohexane-l-carboxylate (sulfo SMCC), and mixed 4 C over night. Un-reacted EpoR was removed by centrifugation through a IOKDa cut off Centricon column (Millipore, Bedford, MA).

2) The soluble extracellular domain (200 mcg) of human EpoR (R&D Systems, Minneapolis, MN) was re-suspended in PBS and mixed with 4 mcg of TCE-BPA (p-Benzoyl Phenylalanine) and incubated under UV light (362 nM) at room temperature for 45 minutes.
The un-reacted EpoR was removed by centrifugation through a IOKDa cut off CentriconTM
column (Millipore, Bedford, MA).

Immunization of animals. Monoclonal antibodies of the invention, including Ab12 and Ab198 (also referred to herein as AB-ABT2-XG2-012 and AB-ABT2-XG2-198, respectively) were developed by immunizing XenoMouse mice (XenoMouse XG2, Abgenix, Inc., Fremont, CA and Vancouver, BC) with soluble EpoR coupled to a TCE as described above.
The initial immunization was with 20 mcg of antigen and mixed 1:1 v/v with Complete Freund's Adjuvant (CFA) (Sigma, St Louis, MO) per mouse. The subsequent immunizations were with 20 mcg of antigen mixed 1:1 v/v with incomplete Freund's (IFA). In particular, each animal was immunized at the base of tail and by intraperitoneal injection on days 0, 14, 28 and 42.

Biotinylation of EpoR. 300 mcg of EpoR (Abbott CHO cell derived ref.#
RB69084:4) was re-suspended in 990 mcL of PBS pH 8.6 and added to 100 mcg of biotin-NHS
(Pierce, Rockford, 111) dissolved in DMSO (Dimethyl Sulfoxide) incubated for forty minutes at room temperature (RT). Free biotin and buffer was removed by centrifugation through a 5kDa Centricon column with several washes with PBS pH 7.4 and re-suspended in an appropriate volume to a final concentration was 600 mcg/mL.

Selection of animals for harvest. Anti-EpoR antibody titers were determined by ELISA. 0.7 mcg/ml biotin EpoR (described above) was coated onto streptavadin plates (Sigma, St Louis, MO) at room teperature for 1 hour. The solution containing unbound biotin EpoR
was removed and all plates were washed five times with dH2O. XenoMouse sera from the EpoR immunized animals, or naive XenMouse animals, were titrated in 2%milk/PBS at a 1:2 dilution in duplicate from a 1:100 initial dilution. The last well was left blank, and plates were washed five times with dH2O. A goat anti-human IgG Fe-specific horseradish peroxidase (HRP)(Pierce, Rockford, IL) conjugated antibody was added at a final concentration of 1 mcg/mL for 1 hour at room temperature. The plates were washed five times with dH2O. The plates were developed with the addition of TMB chromogenic substrate (KPL, Gaithersburg, MD) for 30 minutes and the ELISA was stopped by the addition of 1 M phosphoric acid. The specific titers obtained from XenoMouse animals were determined from the optical density at 450 nm and are shown in Table 1. The titer represents the reciprocal dilution of the serum and therefore the higher the number the greater the humoral immune response to EpoR.

Table 1 Mouse I.D. Titer XenoMouse animal 14 was selected for harvest based on the serology data in Table 1.
Culture and selection of B cells. B cells from the harvested animals were cultured and those secreting EpoR-specific antibodies were isolated essentially as described in Babcook et al., Proc. Natl. Acad. Sci. USA, 93:7843-7848 (1996). ELISA, performed as described above for sera titers, was used to identify EpoR-specific wells. Fifty plates cultured at 500 cells/well were screened on biotin EpoR to identify the antigen-specific wells. The data as shown in Table 2 demonstrated the presence of 701 wells with ODs significantly over background (0.05).

Table 2 Optical Density Number of Positives 0.1 701 0.2 273 0.3 163 0.4 130 0.5 102 0.6 91 0.7 76 0.8 70 0.9 67 1.0 65 2.0 25 3.0 7 These data indicated a very low frequency of hits and indicated that the wells were monoclonal for antigen-specificity. These 701 positive wells were re-screened on biotin EpoR
and 137 wells (shown in bold in Table 3 below) were found to repeat as real antigen-specific wells with ODs significantly over background (0.05).

Table 3 Optical Density Number of Positives 0.1 207 0.15 137 0.2 110 0.3 94 0.4 85 0.5 79 0.6 71 0.7 63 0.8 57 0.9 53 1.0 50 2.0 32 3.0 13 Agonist activity assay. Proliferation of an Epo responsive cell line was used as the basis for the agonist screen. These 137 wells were then screened for agonist activity using the human erythroleukemia cell line UT-7/Epo (Abbott ref#.RB29454-174). 12.5 mcL
of supernatant were added to 1 x 105 cells per well in RPMI 1640 (10% FCS) to a final volume of, 50 mcL in a half-area 96 well plate. The well size is half the area of a typical 96 well plate.
Proliferation was identified visually and compared to cells in media containing a titration of human Epo or no Epo as a base line control. Eleven wells with proliferation activity were identified.

EpoR-specific Hemolytic Plaque Assay. A number of specialized reagents are needed to conduct the assay. These reagents were prepared as follows.
Biotinylation of Sheep red blood cells (SRBC): SRBC are stored in RPMI media as a 25% stock. A 250u1 SRBC packed-cell pellet was obtained by aliquoting 1.0 ml of the stock into a 15-m1 falcon tube, spinning down the cells and removing the supernatant. The cell pellet was then re-suspended in 4.75 ml PBS at pH 8.6 in a 50 ml tube. In a separate 50ml tube, 2.5 mg of Sulfo-NHS biotin was added to 45 ml of PBS at pH 8.6. Once the biotin had completely dissolved, 5 ml of SRBCs were added and the tube rotated at RT for 1 hour. The SRBCs were centrifuged at 3000g for 5 min, the supernatant drawn off and 25 mis PBS at pH
7.4 as a wash.
The wash cycle was repeated 3 times, then 4.75 ml immune cell media (RPMI 1640 with 10%
FCS) was added to the 250 ul biotinylated-SRBC (B-SRBC) pellet to gently re-suspend the B-SRBC (5% B-SRBC stock). Stock was stored at 4 C until needed.

Streptavidin (SA) coating of B-SRBC: One ml of the 5% B-SRBC stock was transferred into to a fresh eppendorf tube. The B-SRBC cells were pelleted with a pulse spin at 8000 rpm (6800 ref) in a microfuge, the supernatant drawn off, the pellet re-suspended in 1.0 ml PBS at pH 7.4, and the centrifugation repeated. The wash cycle was repeated 2 times, then the B-SRBC pellet was resuspended in 1.0 ml of PBS at pH 7.4 to give a final concentration of 5%
(v/v). 10 ul of a 10mg/ml streptavidin (CalBiochem, San Diego, CA) stock solution was added and the tube mixed and rotated at RT for 20min. The washing steps were repeated and the SA-SRBC were re-suspended in lml PBS pH 7.4 (5% (v/v)).
EpoR coating of SA-SRBC: The SA-SRBC were coated with biotinylated EpoR at IOug/ml, the mixed and rotated at RT for 20 min. The SRBC were washed twice with 1.0 ml of PBS at pH 7.4 as above. The EpoR-coated SRBC were re-suspended in RPM!
(+10%FCS) to a final concentration of 5% (v/v).

Determination of the quality of EpoR-SRBC by immunofluorescence (In: 10 ul of 5%
SA-SRBC and 10 ul of 5% PTH-coated SRBC were each added to separate fresh 1.5 ml eppendorf tube containing 40u1 of PBS. The murine anti-EpoR antibody (R&D
Systems Cat.#
MAB307) was added to each sample of SRBCs at 20ug/ml. The tubes were rotated at RT for 25 min, and the cells were then washed three times with 100ul of PBS. The cells were re-suspended in 50ul of PBS and incubated with 40 mcg/mL Gt-anti mouse IgG Fc antibody conjugated to A1exa4887(Molecular Probes, Eugene, OR). The tubes were rotated at RT for 25 min, and then washed with 100ul PBS and the cells re-suspended in 10 ul PBS.
lOul of the stained cells were spotted onto a clean glass microscope slide, covered with a glass coverslip, observed under fluorescent light, and scored on an arbitrary scale of 0-4.

Preparation of plasma cells: The contents of a single microculture well identified by the previous assays as containing a B cell clone secreting the immunoglobulin of interest were harvested. Using a 100-1000 ul PipettmanTM, the contents of the well were recovered by adding 37C RPMI (+10% FCS). The cells were re-suspended by pipetting and then transfered to a fresh 1.5 ml eppendorf tube (final vol. approx 500-700u1). The cells were centrifuged in a microfuge at 1500 rpm (240 rcf) for 2 minutes at room temperature, then the tube rotated 180 degrees and spun again for 2 minutes at 1500 rpm. The freeze media was drawn off and the immune cells resuspended in 100 ul RPMI (10% FCS), then centrifuged. This washing with RPMI (10% FCS) was repeated and the cells re-suspended in 60u1 RPMI (FCS) and stored on ice until ready to use.

Plaque assay: Glass slides (2 x 3 inch) were prepared in advance with silicone edges and allowed to cure overnight at RT. Before use the slides were treated with approx. 5u1 of SigmaCoat (Sigma, Oakville, ON) wiped evenly over glass surface, allowed to dry and then wiped vigorously. To a 60u1 sample of cells was added 60u1 each of EpoR-coated SRBC (5%
v/v stock), 4x guina pig complement (Sigma, Oakville, ON) stock prepared in RPMI with 10%
FCS, and 4x enhancing sera stock (1:900 in RPMI with 10% FCS). The mixture (3 -5u1) was spotted onto the prepared slides and the spots covered with undiluted paraffin oil. The slides were incubated at 37 C for a minimum of 45 minutes.
Plaque assay results: The coating was determined qualitatively by immunofluorescent microscopy to be very high (4/4) using MAB307 to detect coating compared to a secondary detection reagent alone (0/4). There was no signal detected using the MAB307 antibody on red blood cells that were only coated with streptavidin (0/4). These red blood cells were then used to identify antigen-specific plasma cells from the fourteen wells identified in Table 4.
After micromanipulation to rescue the antigen-specific plasma cells, the genes encoding the variable region genes were rescued by RT-PCR on a single plasma cell.

Table 4 Plate ID Single Cell numbers 29G8 ABT2-SCX-1-l 1 431112 ABT2-SCX-185-201,233-239 Expression. After isolation of the single plasma cells, mRNA was extracted and reverse transcriptase PCR was conducted to generate cDNA. The cDNA encoding the variable heavy and light chains was specifically amplified using polymerase chain reaction. The variable heavy chain region was cloned into an IgG2 expression vector. This vector was generated by cloning the constant domain of human IgG2 into the multiple cloning site of pcDNA3. I +/Hygro (Invitrogen, Burlington, ON). The variable light chain region was cloned into an IgK expression vector. This vector was generated by cloning the constant domain of human IgK into the multiple cloning site of pcDNA3.1+/Neo (Invitrogen, Burlington, ON).
The appropriate pairs of heavy chain and the light chain expression vectors were then co-lipofected into a 60 mm dish of 70% confluent human embryonal kidney 293 cells and the transfected cells were left to secrete a recombinant antibody for 24 hours.
The supernatant (3 mL) was harvested from the HEK 293 cells and the secretion of an intact antibody (AB-ABT2-XG2-012 and AB-ABT2-XG2-198) was demonstrated with a sandwich ELISA to specifically detect human IgG (Table 5, fourth column). The specificity of AB-ABT2-XG2-012 and AB-ABT2-XG2-198 was assessed through binding of the recombinant antibody to biotinylated EpoR using ELISA (Table 5, fifth column).

Table 5 Well ID Single cell number Secretion Binding 11G10 ABT2-SCX-254 1:4 1:8 21D1 ABT2-SCX-054 >1:64 >1:64 2503 ABT2-SCX-135 1:4 1:4 29G8 ABT2-SCX-003 >1:64 >1:64 33G8 ABT2-SCX-012 >1:64 >1:64 37A11 ABT2-SCX-022 >1:64 >1:64 43H12 ABT2-SCX-198 >1:64 >1:64 16F7 ABT2-SCX-267 >1:64 >1:64 24C3 ABT2-SCX-060 >1:64 >1:64 24F8 ABT2-SCX-102 >1:64 >1:64 34D4 ABT2-SCX-145 >1:64 >1:64 The ELISA for antigen specific antibody secretion was performed as follows.
Control plates were coated with 2mg/mL Goat anti-human IgG H+L 0/N. For the binding plates, biotin-EpoR (0.7 mcg/mL) was coated onto streptavadin 96 well plates (Sigma, St Louis, MO) for one hour at room temperature. The plates were washed five times with dH2O.
Recombinant antibodies were titrated 1:2 for 7 wells from the undiluted minilipofection supernatant. The plates were washed five times with dH2O. A goat anti-human IgG Fc-specific HRP-conjugated antibody was added at a final concentration of 1 ug/mL
for 1 hour at RT for the secretion and the binding ELISA. The plates were washed five times with dH20.
The plates were developed with the addition of TMB chromogenic substrate (KPL, Gaithersburg, MD) for 30 minutes and the ELISA was stopped by the addition of phosphoric acid. Each ELISA plate was analyzed to determine the optical density of each well at 450 nm.

Purification of AB-ABT2-XG2-012 and AB-ABT2-XG2-198. For larger scale production, the heavy and light chain expression vectors (2.5 ug of each chain/dish) were lipofected into ten 100 mm dishes that were 70% confluent with HEIR 293 cells.
The transfected cells were incubated at 37 C for 4 days, the supernatant (6 mL) was harvested and replaced with 6 mL of fresh media. At day 7, the supernatant was removed and pooled with the initial harvest (120 mL total from 10 plates). The ABT2-XG2-012 and ABT2-antibody were purified from the supernatant using a Protein-A Sepharose (Amersham Biosciences, Piscataway, NJ) affinity chromatography (1 mL). The antibody was eluted from the Protein-A column with 500 mcL of 0.1 M Glycine pH 2.5. The eluate was dialysed in PBS
pH 7.4 and filter sterilized. The antibody was analyzed by non-reducing SDS-PAGE to assess purity and yield.

Agonist activity of recombinant antibodies. The ability of these recombinant antibodies to stimulate the proliferation of Epo responsive cells was examined using the UT-7/Epo cells with proliferation quantitated by MTS reagent (Promega, Madison, WI) measured at 490 nm as described in the Agonist Activity Assay above. ABT2-SCX-012 and ABT2-SCX-198 induced proliferation in comparison to cells in media without antibody and are shown below (Fig. 14 and 15 respectively).

Effect of anti-Human Fc. It is possible that the agonist activity of ABT2-SCX-012 and ABT2-SCX-198 are due to self-aggregation. In order to address this issue we induced aggregation by the addition of an anti-human Fc secondary antibody and the effect on the agonist activity of ABT2-SCX-012 and ABT2-SCX-198 was determined using the UT-7/Epo cells. As shown below the addition of a secondary antibody had no effect on the activity of ABT2-SCX-198 (Fig. 16) and inhibited the activity of ABT2-SCX-012 (Fig. 4 17).

Since the addition of secondary Ab inhibited the activity of ABT2-SCX-012 we concluded that aggregation of this antibody interferes with it's activity and thus it is unlikely that ABT2-SCX-012 has agonist activity due to aggregation. However, the results of ABT2-SCX-198 are more difficult to interpret. The lack of an effect could suggest that ABT2-SCX-198 is fully aggregated and thus the addition of secondary Ab has no further effects on its activity. Alternatively, the lack of effect suggests the activity of ABT2-SCX-198 is not perturbed by the conformational restrictions applied by a secondary antibody.

Sequence analysis of ABT2-SCX-012 and ABT2-SCX-198 The variable heavy chains and the variable light chains for antibodies ABT2-SCX-012 and ABT2-SCX-198 were sequenced to determine their DNA sequences. The complete sequence information for the anti-EpoR antibodies shown in Figures 1, 2, and 18-30 with nucleotide and amino acid sequences for each variable region of the heavy chain gamma and kappa light chains. Figures 1 and 2 provide full-length sequences, including the constant regions.

The variable heavy sequences were analyzed to determine the VH family, the D-region sequence and the J-region sequence. The sequences were then translated to determine the primary amino acid sequence (Fig.29) and compared to the germline VH, D and J-region sequences to assess somatic hypermutations. The primary amino acid sequences of all the anti-EpoR antibody gamma chains are shown in Figure 16. The germline sequences are shown above and the mutations are indicated with the new amino acid sequence.
Unaltered amino acids are indicated with a dash (-). The light chain was analyzed similarly to determine the V
and the J-regions and to identify any somatic mutations from germline kappa sequences (Figure 30). The heavy chain of ABT2-SCX-012 was shown to utilize the VH 4-59 (DP-71), DIR4rc and the JH4a gene segments, while the light chain was shown to use the VkI (A30) and the Jkl gene segments. The heavy chain of ABT2-SCX-198 was shown to utilize the VH 3-30 (V3-30), D4-23 and the JH6b gene segments, while the light chain was shown to use the VkI
(L5) and the Jk3 gene segments.

EXAMPLE 2: Competition of Ab12 with 125I-Labeled EPO for Binding CHO Cells Expressing Recombinant EPO Receptor CHO cells expressing the full length recombinant human EPO receptor were plated at 5x105 cells/well in 24 well plates 72 hours prior to the assay. On the day of the assay, 95u1 of Abl2, Ab198, or EPO at indicated concentrations (shown in Figure 5) diluted in RPMI 1640, 0.5% BSA, 1mM Na N3 and 5 ul (6ng) of 125I-EPO (Amersham Cat. #IM178, Arlington Heights,IL 486ci/mM) were added to the wells. After incubating at 37 C for 1.5 hours, the wells were washed three times with cold HBSS and harvested using 0.5m10.IN
NaOH.
Samples were counted in a Micromedic ME Plus gamma counter. The results are shown in Figure 5. Specifically, the results show that Abs 12 and 198 competed with EPO
for binding to the erythropoietin receptor.

EXAMPLE 3: Biacore Studies The studies described below were performed on a Biacore 2000 utilizing the Biacontrol software version 3.1. (Biacore, Uppsala, Sweden). Binding analyses were performed with antibody immobilized directly to the chip surface and followed by injection of varying receptor concentrations.

Immobilization of Antibody Immobilizations of antibody were performed using the default immobilization program in the BiacoreM
software package. Antibodies were diluted to 10 ug/mL in the supplied acetate buffers to prescreen for the appropriate pH at which to conduct the immobilizations. For inuuobilizations, antibodies were diluted into the appropriate acetate buffer (10 mM acetate pH
4.0) and coupled directly to the chip surface using standard EDC chemistry at three different protein levels (500, 1000, and 1500 RU). The fourth flow cell was mock coupled with EDC to cap the carboxyl groups and provide a background surface as a negative control.

Binding studies Binding studies were performed by successive injections of varying concentrations of soluble human EPO receptor over the chip surface (500 RU immobilized protein).
Binding analyses were performed in the supplied HBS-EP buffer [HBS buffer -10 mM HEPES
pH -7.4, 150 mM NaCl, 3 mM EDTA, 0.005% Polysorbate 20 (v/v), Biacore] using receptor diluted to the desired concentrations (10 - 200 nM) using the running buffer (HBS-EP).
Experiments were performed at a flow rate of 30 uL/min. The receptor was injected over a period of 3 minutes followed by a 15 minute dissociation period. Simultaneous injections over the flow cell created as a negative control were also performed. All injections were performed in triplicate.

Model fitting Data were fit to the models available in the BiaEvaluation 3Ø2 software package (Biacore). The data points from the experimental injections were corrected by subtraction of data points from simultaneous over the negative control surface. The corrected data were used to fit to the 1:1 (Langmuir) binding model as well as the bivalent analyte model available in the BiaEvaluation software package. Dissociation constants were calculated directly from fitting to the Langmuir binding model. For the bivalent analyte model, the dissociation constants were calculated indirectly using the calculated values for the kinetic dissociation and kinetic association constants, kd and ka.

Table 6 Antibody kD
Ab12 17.5nM
Ab 198 13.9 nM

EXAMPLE 4: EPO Dependent Human Cell Proliferation Assay Stock cultures of the human erythroleukemic cell line, F36E cells were maintained in RPMI 1640 media with 10% fetal bovine serum and 1 unit per mL of recombinant human erythropoietin. Prior to assays, cells were cultured overnight at a density of 4.0 to 5.0 x 105 cells per mL in growth medium without EPO. Cells were recovered, washed and resuspended at a density of 1.0 x 106 cells per mL in assay medium (RPMI 1640 + 10% FBS) and 50 uL of cells added to wells of a 96 well microtiter plate. 50 uL of each of Ab12, Ab 390, Ab 412, Ab 467, Ab 484, Ab 430/432 and Ab198 or EPO standards (recombinant human EPO
(rHuEPO)) in assay medium were added to wells and the plates were incubated in a humidified incubator at 37 C with a 5% CO2 atmosphere. After 72 hours, 20 gL of Promega Cell Titer Aqueous reagent (as prepared per manufacturer's instructions, Madison, Wisconin) was added to all wells. Plates were incubated at 37 C with a 5% CO2 atmosphere for 4 hours and the optical density at 490 nm was determined using a microplate reader (Wallac Victor 1420 Multilabel Counter, Wallac Company, Boston, MA). The results are shown in Figure 6. All Abs stimulated proliferation of the F36E cell line. Maximal proliferative activity was similar to that observed with the EPO control and shown by a bell shaped curve as concentration increased. The results in Figure 7 demonstrate that Abl2, after storage at 4 C
for up to 20 days, is active in inducing the proliferation of F36E cells. Proliferative activity was similar to that observed with the EPO control with the maximal response differing about ten-fold on a molar equivalent basis EXAMPLE 5: Human CD36+ CFUe Assay Frozen human CD36+ erythroid progenitor cells obtained from Poietics (Biowhittaker (Walkersville, MD)) were thawed and 104 cells/ml in IMDM-2%FBS. Cells (0.3 ml) were added to 0.3 ml tubes containing 2.4 ml Methocult (StemCell Technologies, Vancouver, Canada) Cat. #04230), 0.3 ml stem cell growth factor (Sigma, St. Louis, Missouri Cat. #S7901, 100ug/ml), and 0.3 ml EPO (R&D Systems), Ab 12, or IMDM-2% FBS. After mixing, 1.1 ml of the Methocult suspension was added to a 35 mm non tissue culture treated sterile petri dish and incubated at 37 C, 5% CO2 for 2 weeks. Colonies were identified microscopically. The results are shown in Figure 8. Specifically, Ab12 induced the formation of CFU-E colonies from human CD 36+ progenitor cells. The colonies, identified microscopically, were red in color. The size and number of the colonies is reduced compared to those observed with the EPO
control probably due to a reduced proliferative signal.
EXAMPLE 6: Demonstration of Erythopoietic Activity in Liquid Cultures CD34+ cells were enriched from human peripheral blood using a Direct CD34+
Progenitor Cell Isolation Kit (Miltenyi, Auburn, CA). Recovered cells were washed twice with alpha-medium and re-suspended in suspension culture media (alpha-media supplemented with 30% FCS, 1% deionized BSA, 10-5M (3-mercaptoethanol, 10"6 M dexamethasone, 0.3 mg/mL
human hollo-transferrin and 10 ng/mL human recombinant stem cell factor).
Cells were plated out at a density of 1 x 104 cells/mL in duplicates in 6-well microplates with test antibody at concentrations ranging from 0.1 - 100 ng/mL. Plates were incubated at 37 C and 5% CO2 for two weeks. Duplicate samples from each well were recovered for cell counts and staining with benzidine (Reference Fibach, E., 1998 Hemoglobin, 22:5-6, 445-458).

The results are shown in Figure 9. Specifically, Ab198 induced the proliferation of human erythroid producing cells derived from progenitor cells in a dose dependent manner.
The number of proliferating cells and the percentage expressing hemoglobin, as indicated by staining with benzidine, was reduced compared to the EPO treated controls again probably due to a reduced proliferative signal.

EXAMPLE 7: Cynomolgus Bone Marrow CFUe Assay Bone marrow was harvested from cynoinolgus monkeys and diluted 1:2 with PBS.
Three ml of the diluted bone marrow was layered over six ml of Lymphoprep (Gibco (Invitrogen), Carlsbad, CA Cat. #1001967), centrifuged at 2700rpm for 20 minutes and the buffy coat recovered and diluted in l Oml IMDM-2%FBS. Cells were centrifuged and resuspended at 106cells/ml in IMDM-2%FBS. Cells (0.3 ml) were added to tubes containing 2.4 ml Methocult (StemCell Technologies, Vancouver, Canada) Cat. #04230), 0.3 ml stem cell growth factor (Sigma, Cat. #S7901, 100 ug/ml), 0.3 ml EPO (R& D Systems, Minneapolis, Minnesota), test antibody (Ab198), or IMDM-2%FBS. After mixing, 1.lml of the Methocult suspension was added to a 35mm non tissue culture treated sterile petri dish and incubated at 37 C, 5%C02 for 2 weeks. Colonies were identified microscopically. The results of this assay are shown in Figure 10 demonstrate that Ab 198 induced the formation of CFU-E
colonies (although the number of colonies was reduced compared to that observed with the EPO
control).

EXAMPLE 8: ELISA to Measure Binding of SE-3 Peptide 96 well polystyrene plates (Dynatec (Elk Grove Village, IL) Immunolon 4) were coated with 80 ul of 5ug/ml soluble EPO receptor (sEPOR) (R&D Systems (Minneapolis, MN) Cat.
#307-ER/LF), or peptide SE-3 (PGNYSFSYQLEDEPWKLCRLHWAPTARGAV) (described in U.S. Patent 6,319,499) diluted in 0.015M Na2CO3, 0.035M NaHCO3, pH 9.4 for 2 hours at room temperature and overnight at 4 C. Plates were blocked for 30 minutes at room temperature with 100 ul of 5%BSA in PBS (Gibco (Invitrogen (Carlsbad, CA)) Cat.#10010).
After removal of blocking solution, 50 ul of Ab12 at 5 ug/ml in PBS with 1%
BSA was added to wells and plates were incubated at room temperature for 2 hours. Plates were washed three TM
times using a Skatron 400 Plate Washer with PBS/0.05% Tween 20 and 50 ul of secondary TM
antibody diluted in PBS/0.25%BSA/0.05%Tween 20 added to the wells. For Ab12, goat anti-human IgG (Fc)-HRP (Caltag (Burlingame, CA) Cat.#H 10507) diluted 1:1000 was used and for Ab 71A (available from the American Type Culture Collection HB11689, also described in U.S. Patent 6,319,499), goat anti mouse IgG (Fc)-HRP (Jackson Laboratories (West Grove, PA) Cat.# 115-03 5-164) diluted 1:5000 was used.
After a 1 hour incubation at room temperature, plates were washed three times as before and 50 ul of OPD
Developing Reagent (Sigma #P9187) added to each well. Color development was stopped by addition of 50ul of IN HC1 to the wells and optical density measured at 490nm on a Victor 1420 Multi-Label Counter.

Figure 11 shows that Ab12 does not interact (i.e. bind) with SE-3 peptide. Ab does interact (i.e. binds) with the SE-3 peptide Both Abs 12, and 71A
interacted with immobilized erythropoietin receptor.
EXAMPLE 9: EPO Dependent Proliferation Assay Primary hybridoma supernatants were diluted in assay medium and tested for their ability to stimulate the proliferation of the F36E human erythroleukemic cells as described in EXAMPLE 5. Results with five primary supernatants are shown in Figure 12.
These samples stimulated the proliferation of F36E cells .

EXAMPLE 10: ELISA to Measure Binding of Hybridoma Supernatants to SE-3 Peptide Forty-two primary hybridoma supernatants were tested for their ability to bind to either immobilized EPO receptor or peptide SE-3 as described in EXAMPLE 10. Figure 13 shows that whereas all the hybridoma supernatants tested interact with immobilized EPO receptor, only sample 16 interacted with SE-3 peptide at levels above background.

EXAMPLE 11: Comparison of Erythropoietic Activity of Gamma-1 Ab12 versus Gamma-2 Ab12 Proliferation assays (as described in Example 4) were performed to compare the erythropoietic activity of gamma-1 Ab 12 and gamma-2 Ab 12 on F36e human erythroleukemic cells. The results are shown in Figure 31. As Figure 31 shows, gamma-2 Ab 12 was more effective at stimulating proliferation of the F3 6E cell line than gamma-1 Ab 12.
EXAMPLE 12: Effect of Ab 12 on Erythropoiesis in vivo (a) Construction of mEpoR -/-, hEopR + transgenic mice: Transgenic mice that produced only human EpoR (hEpoR+, single allele) and no endogenous mouse EpoR
(mEpoR
-/-, double allele mutation) were generated as described in Liu, C. et al., Jounal of Biological Chemistry, 272:32395 (1997) and Yu, X., et al., Blood, 98(2):475 (2001).
Breeding colonies were established to generate mice for in vivo studies of eryhthropoiesis.
(b) Multiple dosing regimen: In initial experiments, animals were subjected to a multiple dosing regimen of Ab 12 to determine whether the antibody would cause an increase 15, in reticulocyte counts and/or % hematocrit. Five transgenic mice (mEpoR -/-, hEpoR+, were injected subcutaneously with either 5 gg or 50 gg of Ab 12 in 0.2 mL vehicle (phosphate buffered saline [PBS] containing 0.1% bovine serum albumin ([BSA]). Control animals also were injected in the same manner with equal volumes of the vehicle alone or vehicle containing 5U Epogen (Amgen , Thousand Oaks, CA). All animals were dosed over a three-week period in accordance with the following schedule:
Week 1 Week 2 Week 3 Monday, Tuesday, Wednesday, Friday Monday, Wednesday, Friday Monday, Wednesday Sample bleeds were taken on day 4 (Thursday of week 1) for determining reticulocyte counts and on day 19 (Friday of week 3) for determining hematocrits. Reticulocyte counts and hematocrit determinations were made using methods well known in the art. As Figure 32 shows, Ab 12 caused a statistically significant increase (over controls) in reticulocyte count and % hematocrit in animals receiving either 5 or 50 g of Ab 12 antibody.
(c) Weekly dosing regimen: To assess whether the results seen under a multiple dosing regimen still would be observed in animals receiving fewer doses of Ab 12, transgenic mice were injected (as described in (b) above) with varying concentrations (0.5, 2.5, 5.0, 50 and 250 g) of Ab 12 or a control, AranespTM (Amgen, Thousand Oaks, CA), a more active variant of Epogen on days 1, 8 and 15 and bled on days 4 and 19 for determination of reticulocyte count and hematocrit, respectively. Control animals received a single dose of vehicle only or a human IgG2 isotype control. Figure 33 shows that Ab 12 caused a statistically significant increase (over vehicle and isotype controls) in pecent hematocrit with all but the lowest concentrations tested.
(d) Single versus weekly dosing regimens: To determine whether a single dose of Ab-12 would have an effect on erythropoiesis after 3 weeks, 'transgenic mice were dosed with Ab 12 (50 g), at one week intervals for 3 weeks or with a single dose of Ab 12 (150 g) and bled on day 19 for determination of percent hematocrit. Control animals received vehicle alone, a single dose of AranespTM (900 ng) or 3 total doses of AranespTM injected at weekly intervals (300 ng x 3). Figure 34 shows that both dosing regimens of Ab 12 caused a statistically significant increase in percent hematocrit over the vehicle control. In contrast, the single dose regimen of AranespTM did not have this effect.

The present invention is illustrated by way of the foregoing description and examples.
The foregoing description is intended as a non-limiting illustration, since many variations will become apparent to those skilled in the art in view thereof.
Changes can be made to the composition, operation and arrangement of the method of the present invention described herein without departing from the concept and scope of the invention.

SEQUENCE LISTING
<110> Abbott Laboratories <120> Erythropoietin Receptor Binding Antibodies <130> 31760-2200 <140> CA 2,501,984 <141> 2003-10-14 <150> US 10/269,711 <151> 2002-10-14 <150> US 10/684,109 <151> 2003-10-10 <160> 115 <170> FastSEQ for Windows Version 4.0 <210> 1 <211> 30 <212> PRT
<213> Homo sapiens <400> 1 Pro Gly Asn Tyr Ser Phe Ser Tyr Gln Leu Glu Asp Glu Pro Trp Lys Leu Cys Arg Leu His Gln Ala Pro Thr Ala Arg Gly Ala Val <210> 2 <211> 349 <212> DNA
<213> Homo sapiens <400> 2 caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggagac cctgtccctc 60 acctgcactg tctctggtgc ctccatcagt agttactact ggagctggat ccggcagccc 120 ccagggaagg gactggagtg gattgggtat atctattaca gtgggagcac caactacaac 180 ccctccctca agagtcgagt caccatatca gtagacacgt ccaagaacca gttctccctg 240 aagctgaggt ctgtgaccgc tgcggacacg gccgtgtatt actgtgcgag agagcgactg 300 gggatcgggg actactgggg ccaaggaacc ctggtcaccg tctcctcag 349 <210> 3 <211> 116 <212> PRT
<213> Homo sapiens <400> 3 Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Ala Ser Ile Ser Ser Tyr Tyr Trp Ser Trp Ile Arg Gin Pro Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Tyr Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu Lys Ser Arg Val Thr Ile Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu Lys Leu Arg Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Glu Arg Leu Gly Ile Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser <210> 4 <211> 322 <212> DNA
<213> Homo sapiens <400> 4 gacatccagc tgacccaatc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 60 atcacttgcc gggcaagtca gggcattaga aatgatttag gctggtatca gcagaaacca 120 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 240 gaagattttg caacttatta ctgtctacag cataatactt accctccgac gttcggccaa 300 gggaccaagg tggaaatcaa ac 322 <210> 5 <211> 107 <212> PRT
<213> Homo sapiens <400> 5 Asp Ile Gln Leu Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Gly Ile Arg Asn Asp Leu Gly Trp Tyr Gln Gin Lys Pro G1y Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Thr Tyr Pro Pro Thr Phe Gly Gln Gly Thr Lys Val Glu Ile Lys <210> 6 <211> 370 <212> DNA
<213> Homo sapiens <400> 6 caggtgcagc tggtggagtc tgggggaggc gtggtccagc ctgggaggtc cctgagactc 60 tcctgtgtag cctctggatt caccttcagt agctatggca tgcactgggt ccgccaggct 120 ccaggcaagg ggctggagtg ggtggcagtt atatcatatg atggaagtaa taaatactat 180 gcagactccg tgaagggccg attcaccatc tccagagaca attccaagaa cacgctgtat 240 ctgcaaatga acagcctgag agttgaggac acggctgtgt attactgtgc gagagatcac 300 ggtgggaggt acgtctacga ctacggtatg gacgtctggg gccaagggac cacggtcacc 360 gtctcctcag 370 <210> 7 <211> 123 <212> PRT
<213> Homo sapiens <400> 7 Gin Val Gin Leu Val Glu Ser Gly Gly Gly Val Val Gin Pro Gly Arg Ser Leu Arg Leu Ser Cys Val Ala Ser Gly Phe Thr Phe Ser Ser Tyr Gly Met His Trp Val Arg Gin Ala Pro Gly Lys Gly Leu Glu Trp Val Ala Val Ile Ser Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu Gin Met Asn Ser Leu Arg Val Glu Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp His Gly Gly Arg Tyr Val Tyr Asp Tyr Gly Met Asp Val Trp Gly Gin Gly Thr Thr Val Thr Val Ser Ser <210> 8 <211> 322 <212> DNA
<213> Homo sapiens <400> 8 gacatccaga tgacccaatc tccatcttcc gtgtctgcat ctataggaga cagagtctcc 60 atcacttgtc gggcgagtca gggtattagc agctggttag cctggtatca gcagaaacca 120 gggaaagccc ctacgctcct tatctatgct gcatccactt tgcaacgtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagat ttcactctca ccatcagcag cctgcagcct 240 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 300 gggaccaaag tggatatcaa ac 322 <210> 9 <211> 107 <212> PRT
<213> Homo sapiens <400> 9 Asp Ile Gin Met Thr Gln Ser Pro Ser Ser Val Ser Ala Ser Ile Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gin Gly Ile Ser Ser Trp Leu Ala Trp Tyr Gin Gin Lys Pro Gly Lys Ala Pro Thr Leu Leu Ile Tyr Ala Ala Ser Thr Leu Gin Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gin Gin Ala Asn Ser Phe Pro Phe Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys <210> 10 <211> 370 <212> DNA
<213> Homo sapiens <400> 10 caggtgcagc tggtggagtc tgggggaggc gtggtccagc ctgggaggtc cctgagactc 60 tcctgtgcag cctctggatt caccttcagt agctatggca tgcactgggt ccgccaggct 120 ccaggcaagg ggctggagtg ggtggcagtt atatcatatg atggaagtaa taaatactat 180 gcagactccg tgaagggccg attcaccatc tccagagaca attccaagaa cacgctgtat 240 ctgcaaatga acagcctgag agttgaggac acggctgtgt attactgtgc gagagatcac 300 ggtgggaggt acgtctacga ctacggtatg gacgtctggg gccaagggac cacggtcacc 360 gtctcctcag 370 <210> 11 <211> 123 <212> PRT
<213> Homo sapiens <400> 11 Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Tyr Gly Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val Ala Val Ile Ser Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Val Glu Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp His Gly Gly Arg Tyr Val Tyr Asp Tyr Gly Met Asp Val Trp Gly Gin Gly Thr Thr Val Thr Val Ser Ser <210> 12 <211> 322 <212> DNA
<213> Homo sapiens <400> 12 gacatccaga tgacccaatc tccatcttcc gtgtctgcat ctgtaggaga cagagtctcc 60 atcacttgtc gggcgagtca gggtattagc agctggttag tctggtatca gcagaaacca 120 gggaaagccc ctgcgctcct aatctatgct gcatccagtt tgcagcgtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagac ttcactctca ccatcagcag cctgcagcct 240 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 300 gggaccaaag tggatatcaa ac 322 <210> 13 <211> 107 <212> PRT
<213> Homo sapiens <400> 13 Asp Ile Gln Met Thr Gin Ser Pro Ser Ser Val Ser Ala Ser Val Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gln Gly Ile Ser Ser Trp Leu Val Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Ala Leu Leu Ile Tyr Ala Ala Ser Ser Leu Gln Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gin Gln Ala Asn Ser Phe Pro Phe Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys <210> 14 <211> 370 <212> DNA
<213> Homo sapiens <400> 14 caggtgcagc tggtggagtc tgggggaggc gtggtccagc ctgggaggtc cctgagactc 60 tcctgtgcag cctctggatt caccttcagt agctatggca tgcactgggt ccgccaggct 120 ccaggcaagg ggctggagtg ggtggtagtt atatcatatg atggaagtaa taaatactat 180 gcagactccg tgaagggccg attcaccatc tccagagaca attccaagaa cacgctgtat 240 ctgcaaatga acagcctgag agttgaggac acggctgtgt attactgtgc gagagatcac 300 ggtgggaggt acgtctacga ctacggtatg gacgtctggg gccaagggac cacggtcacc 360 gtctcctcag 370 <210> 15 <211> 123 <212> PRT
<213> Homo sapiens <400> 15 Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Sex Ser Tyr Gly Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val Val Val Ile Ser Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Val Glu Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp His Gly Gly Arg Tyr Val Tyr Asp Tyr Gly Met Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val Ser Ser <210> 16 <211> 322 <212> DNA
<213> Homo sapiens <400> 16 gacatccaga tgacccaatc tccatcttcc gtgtctgcat ctgtaggaga cagagtctcc 60 atcacttgtc gggcgagtca gggtattagc agctggttag cctggtatca gcagaaacca 120 gggaaagccc ctacgctcct aatctatgct gcatccagtt tgcaacgtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagat ttcactctca ccatcagcag cctgcagcct 240 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 300 gggaccaaag tggatatcaa ac 322 <210> 17 <211> 107 <212> PRT
<213> Homo sapiens <400> 17 Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Val Ser Ala Ser Val Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gln Gly Ile Ser Ser Trp Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Thr Leu Leu Ile Tyr Ala Ala Ser Ser Leu Gln Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gln Gln Ala Asn Ser Phe Pro Phe Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys <210> 18 <211> 349 <212> DNA
<213> Homo sapiens <400> 18 caggtgcagc tggtggagtc ggggggaggc gtggtccagc ctgggaggtc cctgagactc 60 tcctgtgcag cgtctggatt caccttcagt aaatatggca tgcactgggt ccgccaggct 120 ccaggcaagg ggctggagtg ggtggcagtt ttatggtatg atggaagtaa taaatactat 180 gcagactccg tgaagggccg attcaccatc tccagagaca attccaagaa cacgctgtat 240 ctgcaaatga acagcctgag agccgaggac acggctgtgt attactgtgc gagaggtccg 300 tactactttg actactgggg ccagggaacc ctggtcaccg tctcctcag 349 <210> 19 <211> 116 <212> PRT
<213> Homo sapiens <400> 19 Gln Val Gln Leu Val Glu Ser Gly Gly-Gly Val Val Gin Pro Gly Arg Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Sex Lys Tyr Gly Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val Ala Val Leu Trp Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Ala Glu Asp Thr Ala Val Tyr Tyr Cys Ala Arg Gly Pro Tyr Tyr Phe Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser <210> 20 <211> 325 <212> DNA
<213> Homo sapiens <400> 20 gaaattgtgt tgacgcagtc tccaggcacc ctgtctttgt ctccagggga aagagccacc 60 ctctcctgca gggccagtca gagtgttagc agcagctact tagcctggta ccagcagaaa 120 cctggccagg ctcccaggct cctcatctat ggtgcatcca gcagggccac tggcatccca 180 gacaggttca gtggcagtgg gtctgggaca gacttcactg tcaccatcag cagtctggaa 240 cctgaagatt ttgcagtgta ttactgtcag cagtatggta gttcaccgtg gacgttcggc 300 caagggacca aggtggaaat caaac 325 <210> 21 <211> 108 <212> PRT
<213> Homo sapiens <400> 21 Glu Ile Val Leu Thr Gin Ser Pro Gly Thr Leu Ser Leu Ser Pro Gly Glu Arg Ala Thr Leu Ser Cys Arg Ala Ser Gln Ser Val Ser Ser Ser Tyr Leu Ala Trp Tyr Gin Gin Lys Pro Gly Gln Ala Pro Arg Leu Leu Ile Tyr Gly Ala Ser Ser Arg Ala Thr Gly Ile Pro Asp Arg Phe Ser Gly Ser Gly Her Gly Thr Asp Phe Thr Val Thr Ile Ser Arg Leu Glu Pro Glu Asp Phe Ala Val Tyr Tyr Cys Gin Gin Tyr Gly Ser Ser Pro Trp Thr Phe G1y Gin Gly Thr Lys Val Glu Ile Lys <210> 22 <211> 322 <212> DNA
<213> Homo sapiens <400> 22 gacatccaga tgacccaatc tccatcttcc gtgtccgcat ctgtaggaga cagagtctcc 60 atcacttgtc gggcgagtca gggtattagc agctggttag cctggtatca gcagaaacca 120 gggaaagccc ctacgctcct aatctatgct gcatccagtt tgcaacgtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagat ttcactctca ccatcagcag cctgcagcct 240 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 300 gggaccaaag tggatatcaa ac 322 <210> 23 <211> 107 <212> PRT
<213> Homo sapiens <400> 23 Asp Ile Gin Met Thr Gin Ser Pro Ser Ser Val Ser Ala Ser Val Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gin Gly Ile Ser Ser Trp Leu Ala Trp Tyr Gin Gin Lys Pro Gly Lys Ala Pro Thr Leu Leu Ile Tyr Ala Ala Ser Ser Leu Gln Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gln Gln Ala Asn Ser Phe Pro Phe Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys <210> 24 <211> 322 <212> DNA
<213> Homo sapiens <400> 24 gacatccaga tgacccaatc tccatcttcc gtgtctgcat ctgtaggaga cagagtctcc 60 atcacttgtc gggcgagtca gggtattagc agctggttag cctggtatca gcagaaacca 120 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaacgtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagat ttcactctca ccatcagcag cctgcagcct 240 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 300 gggaccaaag tggatatcaa ac 322 <210> 25 <211> 107 <212> PRT
<213> Homo sapiens <400> 25 Asp Ile Gln Net Thr Gln Ser Pro Ser Ser Val Ser Ala Ser Val Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gln Gly Ile Ser Ser Trp Leu Ala Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gln Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser G1y Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gln Gln Ala Asn Ser Phe Pro Phe Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys <210> 26 <211> 322 <212> DNA
<213> Homo sapiens <400> 26 gacatccaga tgacccagtc tccatcttcc gtgtctacat ctgtaggaga cagagtctcc 60 atcacttgtc gggcgagtca gggtattggc agctggttag cctggtatca gcagaaacca 120 gggcaagccc ctacgctcct aatctatgct gcatccagtt tgcaacgtgg ggtcccatca 180 agattcagcg gcagtggatc tgggacagat ttcactctca ccatcaacag cctgcagcct 240 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 300 gggaccaaag tggatgtcaa ac 322 <210> 27 <211> 107 <212> PRT
<213> Homo sapiens <400> 27 Asp Ile Gln Met Thr Gin Ser Pro Ser Ser Val Ser Thr Ser Val Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gln Gly Ile Gly Ser Trp Leu Ala Trp Tyr Gln Gin Lys Pro Gly Gln Ala Pro Thr Leu Leu Ile Tyr Ala Ala Ser Ser Leu Gln Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Asn Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gln Gln Ala Asn Ser Phe Pro Phe Thr Phe Gly Pro Gly Thr Lys Val Asp Val Lys <210> 28 <211> 322 <212> DNA
<213> Homo sapiens <400> 28 gacatccaga tgacccagtc tccatcttcc gtgtctgcat ctgtaggaga cagagtctcc 60 atcacttgtc gggcgagtca gggtattggc agctggttag cctggtatca gcagaaacca 120 gggcaagccc ctacgctcct aatctatgct gcatccagtt tgcaacgtgg ggtcccatca 180 agattcagcg gcagtggatc tgggacagat ttcactctca ccatcaacag cctgcagcct 240 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 300 gggaccaaag tggatgtcaa ac 322 <210> 29 <211> 107 <212> PRT
<213> Homo sapiens <400> 29 Asp Ile Gin Met Thr Gin Ser Pro Ser Ser Val Ser Ala Ser Val Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gln Gly Ile Gly Ser Trp Leu Ala Trp Tyr Gln Gin Lys Pro Gly Gln Ala Pro Thr Leu Leu Ile Tyr Ala Ala Ser Ser Leu Gln Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Asn Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gln Gln Ala Asn Ser Phe Pro Phe Thr Phe Gly Pro Gly Thr Lys Val Asp Val Lys <210> 30 <211> 349 <212> DNA
<213> Homo sapiens <400> 30 caggtgcagc tggtggagtc tgggggaggc gtggtccagc ctgggaggtc cctgagactc 60 tcctgtgcag cgtctggatt caccttcagt agctatggca tgcactgggt ccgccaggct 120 ccaggcaagg ggctggagtg ggtggcagtt atatggtttg atggaaataa taaattctat 180 gcagactccg tgaagggccg attcaccatc tccagagaca attccaagaa cacgctgtat 240 ctgcaaatga acagcctgag agtcgaggac acggctgtgt attactgtgc gcgaggcggg 300 agctactggg actactgggg ccagggaacc ctggtcaccg tctcctcag 349 <210> 31 <211> 116 <212> PRT
<213> Homo sapiens <400> 31 Gin Val Gin Leu Val Glu Ser Gly Gly Gly Val Val Gin Pro Gly Arg Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Ser Tyr 20 25 30, Gly Net His Trp Val Arg Gln Ala Pro Gly Lys Giy Leu Glu Trp Val Ala Val Ile Trp Phe Asp Gly Asn Asn Lys Phe Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu Gin Met Asn Ser Leu Arg Val Glu Asp Thr Ala Val Tyr Tyr Cys Ala Arg Gly Gly Ser Tyr Trp Asp Tyr Trp Gly Gin Gly Thr Leu Val Thr Val Ser Ser <210> 32 <211> 336 <212> DNA
<213> Homo sapiens <400> 32 gatattgtga tgacccagac tccactcttc tcatttgtca tgattggaca gccggcctcc 60 atctcctgca ggtctaggca aagcctcgta cacagtgatg gaaacaccta cttgaattgg 120 cttcagcaga ggccaggcca gcctccaaga ctcctaattt ataagacttc taaccggttc 180 tctggggtcc cagatagatt cagtggcagt ggggcaggga cagatttcac actgaaaatc 240 agcagggtgg aagctgagga tgtcggggtt tattactgta tgcaagctac acaatttcct 300 atcacgttcg gccaagggac acgactggag attaaa 336 <210> 33 <211> 112 <212> PRT
<213> Homo sapiens <400> 33 Asp Ile Val Met Thr Gin Thr Pro Leu Phe Ser Phe Val Met Ile Gly Gin Pro Ala Ser Ile Ser Cys Arg Ser Arg Gin Ser Leu Val His Ser Asp Gly Asn Thr Tyr Leu Asn Trp Leu Gin Gin Arg Pro Gly Gin Pro Pro Arg Leu Leu Ile Tyr Lys Thr Ser Asn Arg Phe Ser Gly Val Pro Asp Arg Phe Ser Gly Ser Gly Ala Gly Thr Asp Phe Thr Leu Lys Ile Ser Arg Val Glu Ala Glu Asp Val Gly Val Tyr Tyr Cys Met Gin Ala Thr Gln Phe Pro Ile Thr Phe Gly Gln Gly Thr Arg Leu Glu Ile Lys <210> 34 <211> 370 <212> DNA
<213> Homo sapiens <400> 34 caggtgcagc tggtggagtc tggtggaggc gtggtccagc ctgggaggtc cctgagactc 60 tcctgtgcag cctctggatt caccttcagt agctatggca tgcactgggt ccgccaggct 120 ccaggcaagg ggctggagtg ggtggcagtt atatcatatg atggaagtaa taaatactat 180 gcagactccg tgaagggccg attcaccatc tccagagaca attccaagaa cacgctgtat 240 ctgcaaatga acagcctgag agttgaggac acggctgtgt attactgtgc gaaagatcac 300 ggtgggaggt acgtctacga ctacggtatg gacgtctggg gccaagggac cacggtcacc 360 gtctcctcag 370 <210> 35 <211> 123 <212> PRT
<213> Homo sapiens <400> 35 Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg Ser Leu Arg Leu SerCys Ala Ala Ser Gly Phe Thr Phe Sex Ser Tyr Gly Met His Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val Ala Val Ile Ser Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Val Glu Asp Thr Ala Val Tyr Tyr Cys Ala Lys Asp His Gly Gly Arg Tyr Val Tyr Asp Tyr Gly Met Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val Ser Ser <210> 36 <211> 322 <212> DNA
<213> Homo sapiens <400> 36 gacatccaga tgacccagtc tccatcttcc gtgtctgcat ctgtaggaga cagagtctcc 60 atcacttgtc gggcgagtca gggtattggc agctggttag cctggtatca gcagaaacca 120 gggcaagccc ctacgctcct aatctatgct gcctccagtt tgcaacgtgg ggtcccatca 180 agattcagcg gcagtggatc tgggacagat ttcactctca ccatcaacag cctgcagcct 240 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 300 gggaccaaag tggatgtcaa ac 322 <210> 37 <211> 107 <212> PRT
<213> Homo sapiens <400> 37 Asp Ile Gin Met Thr Gin Ser Pro Ser Ser Val Ser Ala Ser Val Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gin Gly Ile Gly Ser Trp Leu Ala Trp Tyr Gin Gin Lys Pro Gly Gin Ala Pro Thr Leu Leu Ile Tyr Ala Ala Ser Ser Leu Gin Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp She Thr Leu Thr Ile Asn Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gin Gin Ala Asn Ser Phe Pro She Thr Phe Gly Pro Gly Thr Lys Val Asp Val Lys <210> 38 <211> 348 <212> DNA
<213> Homo sapiens <400> 38 caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggagac cctgtccctc 60 acctgcactg tctctggtgc ctccatcagt aattactact ggagctggat ccggcagccc 120 ccagggaagg gactggagtg gattgggtat gtctcttaca gtgggagtac gtactacaac 180 ccctccctca agggtcgagt caccatgtca gtagacacgt ccaagaacca gttctccctg 240 aagctgagct ctgtgaccgc tgcggacacg gccgtgtatt actgtgcgag agaaaaactg 300 gggattggag actactgggg ccagggaacc ctggtcaccg tctcctca 348 <210> 39 <211> 116 <212> PRT
<213> Homo sapiens <400> 39 Gin Val Gin Leu Gin Giu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu Thr Leu Ser Leu Thr Cys Thr Val Her Gly Ala Ser Ile Ser Asn Tyr Tyr Trp Ser Trp Ile Arg Gin Pro Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Val Ser Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro Ser Leu Lys Gly Arg Val Thr Met Ser Val Asp Thr Ser Lys Asn Gin She Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Glu Lys Leu Gly Ile Giy Asp Tyr Trp Gly Gin Gly Thr Leu Val Thr Val Ser Ser <210> 40 <211> 322 <212> DNA
<213> Homo sapiens <400> 40 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagattcacc 60 atcacttgcc gggcaagtca gggcattaaa aatgatttag gctggtatca gcagaaacca 120 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 240 gaagattttg caacttatta ctgtctacag cataatagtt atccgtgcag ttttggccag 300 gggaccaagc tggagatcaa ac 322 <210> 41 <211> 107 <212> PRT
<213> Homo sapiens <400> 41 Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Gly Ile Lys Asn Asp Leu Gly Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala'Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro 65 r 70 75 80 Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Ser Tyr Pro Cys Ser Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys <210> 42 <211> 354 <212> DNA
<213> Homo sapiens <400> 42 caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcacagac cctgtccctc 60 acctgcactg tctctggtgc ctccatcagc agtggtgctt actactggag ttggatccgc 120 cagcacccag ggaagggcct ggagtggatt gggtacatct ataagagtga gacctcctac 180 tacaacccgt ccctcaagag tcgacttacc ctatcagtag acacgtctaa gaaccagttc 240 tccctgaacc tgatctctgt gactgccgcg gacacggccg tgtattattg tgcgagagat 300 aaactgggga tcgcggacta ctggggccag ggaaccctgg tcaccgtctc ctca 354 <210> 43 <211> 118 <212> PRT
<213> Homo sapiens <400> 43 Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Gln Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Ala Ser Ile Ser Ser Gly Ala Tyr Tyr Trp Ser Trp Ile Arg Gln His Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Lys Ser Glu Thr Ser Tyr Tyr Asn Pro Ser Leu Lys Ser Arg Leu Thr Leu Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu Asn Leu Ile Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp Lys Leu Gly Ile Ala Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser <210> 44 <211> 322 <212> DNA
<213> Homo sapiens <400> 44 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 60 atcacttgcc gggcaagtca ggacattaga aatgatttag gctggtatca gcagaaacca 120 gggaaagccc ctaagcgcct gatctatgct gcatccaatt tgcaaagtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 240 gaagattttg caacttatta ctgtctacag cataatagct accctcccac tttcggcgga 300 gggaccaagg tggaaatcaa ac 322 <210> 45 <211> 107 <212> PRT
<213> Homo sapiens <400> 45 Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr lie Thr Cys Arg Ala Ser Gin Asp Ile Arg Asn Asp Leu Gly Trp Tyr Gin Gin Lys Pro G1y Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Asn Leu Gin Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Ser Tyr Pro Pro Thr Phe Gly Gly Gly Thr Lys Val Glu Ile Lys <210> 46 <211> 349 <212> DNA
<213> Homo sapiens <400> 46 caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggagac cctgtccctc 60 acctgcactg tctctggtgt ctccatcagt aattactact ggagctggat ccggcagtcc 120 ccagggaagg gactggagtg gattggatat atctattaca gtgggagtcc ctattacaac 180 ccctccctca agagtcgagt cactatatct gcagacacgt ccaagaacca attctccctg 240 aagctgagct ctgtgaccgc tgcggacacg gccatttatt actgtgcgag agaaaaactg 300 gggattggag actactgggg ccagggaacc ctggtcaccg tctcctcag 349 <210> 47 <211> 116 <212> PRT
<213> Homo sapiens <400> 47 Gin Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Val Ser Ile Ser Asn Tyr Tyr Trp Ser Trp Ile Arg Gln Ser Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Tyr Ser Gly Ser Pro Tyr Tyr Asn Pro Ser Leu Lys Ser Arg Val Thr Ile Ser Ala Asp Thr Ser Lys Asn Gln Phe Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Ile Tyr Tyr Cys Ala Arg Glu Lys Leu Gly Ile Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser <210> 48 <211> 322 <212> DNA
<213> Homo sapiens <400> 48 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtcggaga cagagtcacc 60 atcacttgcc gggcaagtca gggcattaga aatgatttag gctggtatca gcagaaacca 120 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 240 gaagattttg caacttatta ctgtctacag cataatagtt accctcccac tttcggccct 300 gggaccaagg tggatatcaa ac 322 <210> 49 <211> 107 <212> PRT
<213> Homo sapiens <400> 49 Asp Ile Gin Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Gly Ile Arg Asn Asp Leu Gly Trp Tyr Gln Gin Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Sex Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Ser Tyr Pro Pro Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys <210> 50 <211> 349 <212> DNA
<213> Homo sapiens <400> 50 caggtgcagc tgcaggagtc gggcccagga ctggtgaagc cttcggagac cctgtccctc 60 acctgcactg tctctggtgg ctccatcagt cgttactact ggagctggat ccggcagccc 120 ccagggaagg gactggagtg gattgggtat gtctcttaca gtgggagcac ctactacaac 180 ccctccctca agagtcgagt caccatatca gtagacacgt ccaagaacca gttctccctg 240 aagctgagct ctgtgaccgc tgcggacacg gccgtgtatt actgtgcgag agataaactg 300 gggattggag actactgggg ccagggaacc ctggtcaccg tctcctcag 349 <210> 51 <211> 116 <212> PRT
<213> Homo sapiens <400> 51 Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Gly Ser Ile Ser Arg Tyr Tyr Trp Ser Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Val Ser Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro Ser Leu Lys Ser Arg Val Thr Ile Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp Lys Leu Gly Ile Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser <210> 52 <211> 322 <212> DNA
<213> Homo sapiens <400> 52 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 60 atcacttgcc gggcaagtca gggcattaga aatgatttag gctggtatca gcagaaaccg 120 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 240 gaagattttg caacttatta ctgtctacag cataatagtt acccgtgcag ttttggccag 300 gggaccaagc tggagatcaa ac 322 <210> 53 <211> 107 <212> PRT
<213> Homo sapiens <400> 53 Asp Ile Gln Net Thr Gin Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Gly Ile Arg Asn Asp Leu Gly Trp Tyr Gln Gin Lys Pro Giy Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Ser Tyr Pro Cys Ser Phe Gly Gln Gly Thr Lys Leu Glu Ile Lys <210> 54 <211> 355 <212> DNA
<213> Homo sapiens <400> 54 ctggtgcagc tgcaggagtc gggcccagga ctggtgaagc ctttacagac cctgtccctc 60 acctgcactg tctctggtgg ctccatcagc agtggtgttt actactggag ctggatccgc 120 cagcacccag ggaagggcct ggagtggatt gggtacatct ataacagtaa gacctcctat 180 tataatccgt ccctcaagag tcgacttacc ctatcagtag acacgtctaa gaaccagttc 240 tccctgaacc tgatctctgt gactgccgcg gacacggccg tgtattactg tgcgagagat 300 aaattgggga tcgcggacta ctggggccag ggaaccctgg tcaccgtctc ctcag 355 <210> 55 <211> 118 <212> PRT
<213> Homo sapiens <400> 55 Gln Val Gin Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Leu Gln Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Gly Ser Ile Ser Ser Gly Val Tyr Tyr Trp Ser Trp Ile Arg Gln His Pro Gly Lys Gly Leu G1u Trp Ile Gly Tyr Ile Tyr Asn Ser Lys Thr Ser Tyr Tyr Asn Pro Ser Leu Lys Ser Arg Leu Thr Leu Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu Asn Leu Ile Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp Lys Leu Gly Ile Ala Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser <210> 56 <211> 322 <212> DNA
<213> Homo sapiens <400> 56 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 60 atcacttgcc ggacaagtca gggcattaga aatgatttag gctggtatca gcagaaacca 120 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 180 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 240 gaagattttg caacttatta ctgtctacag,cataatagct accctcccac tttcggcgga 300 gggaccaagg tggagatcaa ac 322 <210> 57 <211> 107 <212> PRT
<213> Homo sapiens <400> 57 Asp Ile Gin Net Thr Gin Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Thr Ser Gln Gly Ile Arg Asn Asp Leu G1y Trp Tyr Gln Gin Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gin Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gin His Asn Ser Tyr Pro Pro Thr Phe Gly Gly Gly Thr Lys Val Glu Ile Lys <210> 58 <211> 34 <212> PRT
<213> Homo sapiens <400> 58 Gly Ala Ser Ile Ser Ser Tyr Tyr Trp Ser Tyr Ile Tyr Tyr Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu Lys Ser Glu Arg Leu Gly Ile Gly Asp Tyr <210> 59 <211> 41 <212> PRT
<213> Homo sapiens <400> 59 Gly Phe Thr Phe Ser Ser Tyr Gly Met His Val Ile Ser Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys Gly Asp His Gly Gly Arg Tyr Val Tyr Asp Tyr Gly Met Asp Val <210> 60 <211> 34 <212> PRT
<213> Homo sapiens <400> 60 Gly Phe Thr Phe Ser Lys Tyr Gly Met His Val Leu Trp Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys Gly Asp Gly His Tyr Phe Asp Tyr <210> 61 <211> 34 <212> PRT
<213> Homo sapiens <400> 61 Gly Phe Thr Phe Ser Ser Tyr Gly Met His Val Ile Trp Phe Asp Gly Asn Asn Lys Phe Tyr Ala Asp Ser Val Lys Gly Ala Pro Ala Tyr Trp Asp Tyr <210> 62 <211> 27 <212> PRT
<213> Homo sapiens <400> 62 Arg Ala Ser Gln Gly Ile Arg Asn Asp Leu Gly Ala Ala Ser Ser Leu Gln Ser Leu Gln His Asn Thr Tyr Pro Pro Thr <210> 63 <211> 27 <212> PRT
<213> Homo sapiens <400> 63 Arg Ala Ser Gln Gly Ile Ser Ser Trp Leu Ala Ala Ala Ser Thr Leu Gln Arg Gln Gln Ala Asn Ser Phe Pro Phe Thr <210> 64 <211> 29 <212> PRT
<213> Homo sapiens <400> 64 Arg Ala Ser Gln Gly Ile Ser Ser Trp Leu Val Ala Leu Ala Ala Ser Ser Leu Gln Arg Gln Gin Ala Asn Ser Phe Pro Phe Thr <210> 65 <211> 27 <212> PRT
<213> Homo sapiens <400> 65 Arg Ala Ser Gln Gly Ile Ser Ser Trp Leu Ala Ala Ala Ser Ser Leu 1 5 10 15' Gln Arg Gln Gin Ala Asn Ser Phe Pro Phe Thr <210> 66 <211> 27 <212> PRT
<213> Homo sapiens <400> 66 Arg Ala Ser Gln Gly Ile Gly Ser Trp Leu Ala Ala Ala Ser Ser Leu Gln Arg Gln Gln Ala Asn Ser Phe Pro Phe Thr <210> 67 <211> 32 <212> PRT
<213> Homo sapiens <400> 67 Arg Ser Arg Gln Ser Leu Val His Ser Asp Gly Asn Thr Tyr Leu Asn Lys Thr Sex Asn Arg Phe Ser Met Gln Ala Thr Gln Phe Pro Ile Thr <210> 68 <211> 28 <212> PRT
<213> Homo sapiens <400> 68 Arg Ala Ser Gln Ser Val Ser Ser Ser Tyr Leu Ala Gly Ala Ser Ser Arg Ala Thr Gln Gln Tyr Gly Ser Ser Pro Trp Thr <210> 69 <211> 1990 <212> DNA
<213> Homo sapiens <400> 69 atgaagcatc tgtggttctt ccttctccta gtggcagctc ccagatgggt cctgtcccag 60 gtgcagctgc aggagtcggg cccaggactg gtgaagcctt cggagaccct gtccctcacc 120 tgcactgtct ctggtgcctc catcagtagt tactactgga gctggatccg gcagccccca 180 gggaagggac tggagtggat tgggtatatc tattacagtg ggagcaccaa ctacaacccc 240 tccctcaaga gtcgagtcac catatcagta gacacgtcca agaaccagtt ctccctgaag 300 ctgaggtctg tgaccgctgc ggacacggcc gtgtattact gtgcgagaga gcgactgggg 360 atcggggact actggggcca aggaaccctg gtcaccgtct cctcagcctc caccaagggc 420 ccatcggtct tccccctggc gccctgctct agaagcacct ccgagagcac agccgccctg 480 ggctgcctgg tcaaggacta cttccccgaa ccggtgacgg tgtcgtggaa ctcaggcgct 540 ctgaccagcg gcgtgcacac cttcccagct gtcctacagt cctcaggact ctactccctc 600 agcagcgtgg tgaccgtgcc ctccagcaac ttcggcaccc agacctacac ctgcaacgta 660 gatcacaagc ccagcaacac caaggtggac aagacagttg gtgagaggcc agctcaggga 720 gggagggtgt ctgctggaag ccaggctcag ccctcctgcc tggacgcacc ccggctgtgc 780 agccccagcc caaggcagca aggcaggccc catctgtctc ctcccccgga ggcctctgcc 840 cgccccactc atgctcaggg agagggtctt ctggcttttt ccaccaggct ccaggcaggc 900 acaggctggg tgcccctacc ccaggccctt cacacacagg ggcaggtgct tggctcagac 960 ctgccaaaag ccatatccgg gaggaccctg cccctgccct aagccgaccc caaaggccaa 1020 actgtccact ccctcagctc ggacaccttc tctcctccca gatccgagta actcccaatc 1080 ttctctctgc agagcgcaaa tgttgtgtcg agtgcccacc gtgcccaggt aagccagccc 1140 aggcctcgcc ctccagctca aggcgggaca ggtgccctag agtagcctgc atccagggac 1200 aggccccagC tgggtgctga cacgtccacc tccatctctt cctcagcctc acctgtggca 1260 ggaccgtcag tcttcctctt ccccccaaaa cccaaggaca ccctcatgat ctcccggacc 1320 cctgaggtca cgtgcgtggt ggtggacgtg agccacgaag accccgaggt ccagttcaac 1380 tggtacgtgg acggcgtgga ggtgcataat gccaagacaa agccacggga ggagcagttc 1440 aacagcacgt tccgtgtggt ctgcgtcctc accgttgtgc accaggactg gctgaacggc 1500 aaggagtaca agtgcaaggt ctccagcaaa ggcctcccag cccccatcga gaaaaccatc 1560 tccaaaacca aaggtgggac ccgcggggta tgagggccac atggacagag gccggctcgg 1620 cccaccctct gccctgggag tgaccgctgt gccaacctct gtccctacag ggcagccccg 1680 agaaccacag gtgtacaccc tgcccccatc ccgggaggag atgaccaaga accaggtcag 1740 cctgacctgc ctggtcaaag gcttctaccc cagcgacatc gccgtggagt gggagagcaa 1800 tgggcagccg gagaacaact acaagaccac acctcccatg ctggactccg acggctcctt 1860 cttcctctac agcaagctca ccgtggacaa gagcaggtgg cagcagggga acttcttctc 1920 atgctccgtg atgcatgagg ctctgcacaa ccactacacg cagaagagcc tctccctgtc 1980 tccgggtaaa 1990 <210> 70 <211> 1990 <212> DNA
<213> Homo sapiens <400> 70 tttacccgga gacagggaga ggctcttctg cgtgtagtgg ttgtgcagag cctcatgcat 60 cacggagcat gagaagacgt tcccctgctg ccacctgctc ttgtccacgg tgagcttgct 120 gtagaggaag aaggagccgt cggagtccag catgggaggt'gtggtcttgt agttgttctc 180 cggctgccca ttgctctccc actccacggc gatgtcgctg gggtagaagc ctttgaccag 240 gcaggtcagg ctgacctggt tcttggtcat ctcctcccgg gatgggggca gggtgtacac 300 ctgtggttct cggggctgcc ctgtagggac agaggttggc acagcggtca ctcccagggc 360 agagggtggg ccgagccggc ctctgtccat gtggccctca taccccgcgg gtcccacctt 420 tggttttgga gatggttttc tcgatggggg ctgggaggcc tttgttggag accttgcact 480 tgtactcctt gccgttcagc cagtcctggt gcacaacggt gaggacgctg accacacgga 540 acgtgctgtt gaactgctcc tcccgtggct ttgtcttggc attatgcacc tccacgccgt 600 ccacgtacca gttgaactgg acctcggggt cttcgtggct cacgtccacc accacgcacg 660 tgacctcagg ggtccgggag atcatgaggg tgtccttggg ttttgggggg aagaggaaga 720 ctgacggtcc tgccacaggt ggtgctgagg aagagatgga ggtggacgtg tcagcaccca 780 gctggggcct gtccctggat gcaggctact ctagggcacc tgtcccgcct tgagctggag 840 ggcgaggcct gggctggctt acctgggcac ggtgggcact cgacacaaca tttgcgctct 900 gcagagagaa gattgggagt tactcggatc tgggaggaga gaaggtgtcc gagctgaggg 960 agtggacagt ttggcctttg gggtcggctt aggtcagggg cagggtcctc ccggatatgg 1020 cttttggcag gtctgagcca agcacctgcc cctgtgtgtg aagggcctgg ggtaggggca 1080 cccagcctgt gcctgcctgg agcctggtgg aaaaagccag aagaccctct ccctgagcat 1140 gagtggggcg ggcagaggcc tccgggtgag gagacagatg gggcctgcct tgctgccctg 1200 ggctggggct gcacagccgg ggtgcgtcca ggcaggaggg ctgagcctgg cttccagcag 1260 acaccctccc tccctgagct ggcctctcac caactgtctt gtccaccttg gtgttgctgg 1320 gcttgtgatc tacgttgcag gtgtaggtct gggtgccgaa gttgctggag ggcacggtca 1380 ccacgctgct gagggagtag agtcctgagg actgtaggac agctgggaag gtgtgcacgc 1440 cgctggtcag agcgcctgag ttccacgaca ccgtcaccgg ttcggggaag tagtccttga 1500 ctagggagcc cagggcggct gtgctctcgg aggtgcttct agagcagggc gccaggggga 1560 agaccgatgg gcccttggtg gaggctgagg agacggtgac cagggttcct tggccccagt 1620 agtccccgat ccccagtcgc tctctcgcac agtaatacac ggccgtgtcc gcagcggtca 1680 cagacctcag cttcagggag aactggttct tggacgtgtc tactgatatg gtgactcgac 1740 tcttgaggga ggggttgtag ttggtgctcc cactgtaata gatataccca atccactcca 1800 gtcccttccc tgggggctgc cggatccagc tccagtagta actactgatg gaggcaccag 1860 agacagtgca ggtgagggac agggtctccg aaggcttcac cagtcctggg cccgactcct 1920 gcagctgcac ctgggacagg acccatctgg gagctgccac taggagaagg aagaaccaca 1980 gatgcttcat 1990 <210> 71 <211> 241 <212> PRT
<213> Homo sapiens <400> 71 Met Lys His Leu Trp Phe Phe Leu Leu Leu Val Ala Leu Ala Ala Pro Arg Trp Val Leu Ser Gin Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Ala Ser Ile Ser Ser Tyr Tyr Trp Ser Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Tyr Ser Gly Ser Thr Asn Tyr Asn Pro Ser Leu Lys Ser Arg Val Thr Ile Ser Val Ala Ser Pro Thr Ser Lys Asn Gln Phe Ser Leu Lys Leu Arg Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Glu Arg Leu Gly Ile Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gin Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gln Thr Tyr Thr Cys Asn Val Ala Ser Pro His Lys Pro Ser Asn Thr Lys Val Ala Ser Pro Lys Thr Val <210> 72 <211> 12 <212> PRT
<213> Homo sapiens <400> 72 Glu Arg Lys Cys Cys Val Glu Cys Pro Pro Cys Pro <210> 73 <211> 115 <212> PRT
<213> Homo sapiens <400> 73 Ala Pro Pro Val Ala Leu Ala Gly Pro Ser Val Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Net Ile Ser Arg Thr Pro Glu Val Thr Cys Val Val Val Ala Ser Pro Val Ser His Glu Asp Pro Glu Val Gln Phe Asn Trp Tyr Val Ala Ser Pro Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Phe Arg Val Val Ser Val Leu Thr Val Val His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn Lys Gly Leu Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Thr Lys <210> 74 <211> 107 <212> PRT
<213> Homo sapiens <400> 74 Gly Gin Pro Arg Glu Pro Gin Val Tyr Thr Leu Pro Pro Ser Arg Glu Glu Met Thr Lys Asn Gin Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gin Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Met Leu Asp Ser Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg Trp Gin Gin Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr Thr Gin Lys Ser Leu Ser Leu Ser Pro Gly Lys <210> 75 <211> 310 <212> PRT
<213> Homo sapiens <400> 75 Ser Thr Sex Glu Ser Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gin Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gin Thr Tyr Thr Cys Asn Val Asp His Lys Pro Ser Asn Thr Lys Val Asp Lys Thr Val Glu Arg Lys Cys Cys Val Glu Cys Pro Pro Cys Pro Ala Pro Pro Val Ala Gly Pro Ser Val Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr Cys Val Val Val Asp Val Ser His Glu Asp Pro Glu Val Gin Phe Asn Trp Tyr Val Asp Giy Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu Glu Gin Phe Asn Ser Thr Phe Arg Val Val Ser Val Leu Thr Val Val His Gin Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn Lys Gly Leu Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Thr Lys Gly Gin Pro Arg Glu Pro Gin Val Tyr Thr Leu Pro Pro Ser Arg Glu Glu Met Thr Lys Asn Gin Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gin Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Met Leu Asp Ser Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr Val Asp Lys Ser Arg Trp Gin Gin Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr Thr Gin Lys Ser Leu Ser Leu Ser Pro Gly Lys <210> 76 <211> 552 <212> DNA
<213> Homo sapiens <400> 76 atgagggtcc ccgctcagct cctggggctc ctgctgctct ggttcccagg tgccaggtgt 60 aagcttgaca tccagctgac ccaatctcca tcctccctgt ctgcatctgt aggagacaga 120 gtcaccatca cttgccgggc aagtcagggc attagaaatg atttaggctg gtatcagcag 180 aaaccaggga aagcccctaa gcgcctgatc tatgctgcat ccagtttgca aagtggggtc 240 ccatcaaggt tcagcggcag tggatctggg acagaattca ctctcacaat cagcagcctg 300 cagcctgaag attttgcaac ttattactgt ctacagcata atacttaccc tccgacgttc 360 ggccaaggga ccaaggtgga aatcaaacga actgtggctg caccatctgt cttcatcttc 420 ccgccatctg atgagcagtt gaaatctgga actgctagcg ttgtgtgcct gctgaataac 480 ttctatccca gagaggccaa agtacagtgg aaggtggata acgccctcca atcgggtaac 540 tcccaggaga gt 552 <210> 77 <211> 552 <212> DNA
<213> Homo sapiens <400> 77 actctcctgg gagttacccg attggagggc gttatccacc ttccactgta ctttggcctc 60 tctgggatag aagttattca gcaggcacac aacgctagca gttccagatt tcaactgctc 120 atcagatggc gggaagatga agacagatgg tgcagccaca gttcgtttga tttccacctt 180 ggtcccttgg ccgaacgtcg gagggtaagt attatgctgt agacagtaat aagttgcaaa 240 atcttcaggc tgcaggctgc tgattgtgag agtgaattct gtcccagatc cactgccgct 300 gaaccttgat gggaccccac tttgcaaact ggatgcagca tagatcaggc gcttaggggc 360 tttccctggt ttctgctgat accagcctaa atcatttcta atgccctgac ttgcccggca 420 agtgatggtg actctgtctc ctacagatgc agacagggag gatggagatt gggtcagctg 480 gatgtcaagc ttacacctgg cacctgggaa ccagagcagc aggagcccca ggagctgagc 540 ggggaccctc at 552 <210> 78 <211> 184 <212> PRT
<213> Homo sapiens <400> 78 Met Arg Val Pro Ala Gln Leu Leu Gly Leu Leu Leu Leu Trp Phe Pro Gly Ala Arg Cys Lys Leu Asp Ile Gin Leu Thr Gin Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gin Gly Ile Arg Asn Asp Leu Gly Trp Tyr Gin Gin Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gin Ser G1y Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gin His Asn Thr Tyr Pro Pro Thr Phe Gly Gin Gly Thr Lys Val Glu Ile Lys Arg Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gin Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala Lys Val Gin Trp Lys Val Asp Asn Ala Leu Gin Ser Gly Asn Ser Gln Glu Ser <210> 79 <211> 31 <212> PRT
<213> Homo sapiens <400> 79 Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala Lys Val Gin Trp Lys Val Asp Asn Ala Leu Gin Ser Gly Asn Ser Gin Glu Ser <210> 80 <211> 2011 <212> DNA
<213> Homo sapiens <400> 80 atggaattgg ggctccgttg ggttttcctc gttgctcttt taagaggtgt ccagtgtcag 60 gtgcagctgg tggagtctgg gggaggcgtg gtccagcctg ggaggtccct gagactctcc 120 tgtgtagcct ctggattcac cttcagtagc tatggcatgc actgggtccg ccaggctcca 180 ggcaaggggc tggagtgggt ggcagttata tcatatgatg gaagtaataa atactatgca 240 gactccgtga agggccgatt caccatctcc agagacaatt ccaagaacac gctgtatctg 300 caaatgaaca gcctgagagt tgaggacacg gctgtgtatt actgtgcgag agatcacggt 360 gggaggtacg tctacgacta cggtatggac gtctggggcc aagggaccac ggtcaccgtc 420 tcctcagcct ccaccaaggg cccatcggtc ttccccctgg cgccctgctc tagaagcacc 480 tccgagagca cagccgcoct gggctgcctg gtcaaggact acttccccga accggtgacg 540 gtgtcgtgga actcaggcgc tctgaccagc ggcgtgcaca ccttcccagc tgtcctacag 600 tcctcaggac tctactccct cagcagcgtg gtgaccgtgc cctccagcaa cttcggcacc 660 cagacctaca cctgcaacgt agatcacaag cccagcaaca ccaaggtgga caagacagtt 720 ggtgagaggc cagctcaggg agggagggtg tctgctggaa gccaggctca gccctcctgc 780 ctggacgcac cccggctgtg cagccccagc ccagggcagc aaggcaggcc ccatctgtct 840 cctcacccgg aggcctctgc ccgccccagt catgctcagg gagagggtct tctggctttt 900 tccaccaggc tccaggcagg cacaggctgg gtgcccctac cccaggccct tcacacacag 960 gggcaggtgc ttggctcaga cctgccaaaa gccatatccg ggaggaccct gcccctgacc 1020 taagccgacc ccaaaggcca aactgtccac tccctcagct cggacacctt ctctcctccc 1080 agatccgagt aactcccaat cttctctctg cagagcgcaa atgttgtgtc gagtgcccac 1140 cgtgcccagg taagccagcc caggcctcgc cctccagctc aaggcgggac aggtgcccta 1200 gagtagcctg catccaggga caggccccag ctgggtgctg acacgtccac ctccatctct 1260 tcctcagccc cacctgtggc aggaccgtca gtcttcctct tccccccaaa acccaaggac 1320 accctcatga tctcccggac ccctgaggtc acgtgcgtgg tggtggacgt gagccacgaa 1380 gaccccgagg tccagttcaa ctggtacgtg gacggcgtgg aggtgcataa tgccaagaca 1440 aagccaaggg aggagcagtt caacagcacg ttccgtgtgg tcagcgtcct caccgttgtg 1500 caccaggact ggctgaacgg caaggagtac aagtgcaagg tctccaacaa aggcctccca 1560 gcccccatcg agaaaaccat ctccaaaacc aaaggtggga cccgcggggt atgagggcca 1620 catggacaga ggccggctcg gcccaccctc tgccctggga gtgaccgctg tgccaacctc 1680 tgtccctaca gggcagcccc gagaaccaca ggtgtacacc ctgcccccat cccgggagga 1740 gatgaccaag aaccaggtca gcctgccctg cctggtcaaa ggcttctacc ccagcgacat 1800 cgccgtggag tgggagagca atgggcagcc ggagaacaac tacaagacca cacctcccat 1860 gctggactcc gacggctcct tcttcctcta cagcaagctc accgtggaca agagcaggtg 1920 gcagcagggg aacgtcttct catgctccgt gatgcatgag gctctgcaca accactacac 1980 gcagaagagc ctctccctgt ctccgggtaa a 2011 <210> 81 <211> 2011 <212> DNA
<213> Homo sapiens <400> 81 tttacccgga gacagggaga ggctcttctg cgtgtagtgg ttgtgcagag cctcatgcat 60 cacggagcat gagaagacgt tcccctgctg ccacctgctc ttgtccacgg tgagcttgct 120 gtagaggaag aaggagccgt cggagtccag catgggaggt gtggtcttgt agttgttctc 180 cggctgccca ttgctctccc actccacggc gatgtcgctg gggtagaagc ctttgaccag 240 gcaggtcagg ctgacctggt tcttggtcat ctcctcccgg gatgggggca gggtgtacac 300 ctgtggttct cggggctgcc ctgtagggac agaggttggc acagcggtca ctcccagggc 360 agagggtggg ccgagccggc ctctgtccat gtggccctca taccccgcgg gtcccacctt 420 tggttttgga gatggttttc tcgatggggg ctgggaggcc tttgttggag accttgcact 480 tgtactcctt gccgttcagc cagtcctggt gcacaacggt gaggacgctg accacacgga 540 acgtgctgtt gaactgctcc tcccgtggct ttgtcttggc attatgcacc tccacgccgt 600 ccacgtacca gttgaactgg acctcggggt cttcgtggct cacgtccacc accacgcacg 660 tgacctcagg ggtccgggag atcatgaggg tgtccttggg ttttgggggg aagaggaaga 720 ctgacggtcc tgccacaggt ggtgctgagg aagagatgga ggtggacgtg tcagcaccca 780 gctggggcct gtccctggat gcaggctact ctagggcacc tgtcccgcct tgagctggag 840 ggcgaggcct gggctggctt acctgggcac ggtgggcact cgacacaaca tttgcgctct 900 gcagagagaa gattgggagt tactcggatc tgggaggaga gaaggtgtcc gagctgaggg 960 agtggacagt ttggcctttg gggtcggctt aggtcagggg cagggtcctc ccggatatgg 1020 cttttggcag gtctgagcca agcacctgcc cctgtgtgtg aagggcctgg ggtaggggca 1080 cccagcctgt gcctgcctgg agcctggtgg aaaaagccag aagaccctct ccctgagcat 1140 gagtggggcg ggcagaggcc tccgggtgag gagacagatg gggcctgcct tgctgccctg 1200 ggctggggct gcacagccgg ggtgcgtcca ggcaggaggg ctgagcctgg cttccagcag 1260 acaccctccc tccctgagct ggcctctcac caactgtctt gtccaccttg gtgttgctgg 1320 gcttgtgatc tacgttgcag gtgtaggtct gggtgccgaa gttgctggag ggcacggtca 1380 ccacgctgct gagggagtag agtcctgagg actgtaggac agctgggaag gtgtgcacgc 1440 cgctggtcag agcgcctgag ttccacgaca ccgtcaccgg ttcggggaag tagtccttga 1500 ccaggcagcc cagggcggct gtgctctcgg aggtgcttct agagcagggc gccaggggga 1560 agaccgatgg gcccttggtg gaggctgagg agacggtgac cgtggtccct tggccccaga 1620 cgtccatacc gtagtcgtag acgtacctcc caccgtgatc tctcgcacag taatacacag 1680 ccgtgtcctc aactctcagg ctgttcattt gcagatacag cgtgttcttg gaattgtctc 1740 tggagatggt gaatcggccc ttcacggagt ctgcatagta tttattactt ccatcatatg 1800 atataactgc cacccactcc agccccttgc ctggagcctg gcggacccag tgcatgccat 1860 agctactgaa ggtgaatcca gaggctacac aggagagtct cagggacctc ccaggctgga 1920 ccacgcctcc cccagactcc accagctgca cctgacactg gacacctctt aaaagagcaa 1980 cgaggaaaac ccagcggagc cccaattcca t 2011 <210> 82 <211> 252 <212> PRT
<213> Homo sapiens <400> 82 Met Glu Leu Gly Leu Arg Trp Val Phe Leu Val Ala Leu Ala Leu Leu Arg Gly Val Gln Cys Gln Val Gln Leu Val Glu Ser Gly Gly Gly Val Val Gln Pro Gly Arg Ser Leu Arg Leu Ser Cys Val Ala Leu Ala Ser Gly Phe Thr Phe Ser Ser Tyr Gly Met His Trp Val Ala Arg Gly Gln Ala Pro Gly Lys Gly Leu Glu Trp Val Ala Leu Ala Val Ile Ser Tyr Asp Gly Ser Asn Lys Tyr Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ser Lys Asn Thr Leu Tyr Leu Gln Met Asn Ser Leu Arg Val Glu Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp His Gly Gly Arg Tyr Val Tyr Asp Tyr Gly Met Asp Val Trp Gly Gln Gly Thr Thr Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Her Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gln Thr Tyr Thr Cys Asn Val Ala Ser Pro His Lys Pro Ser Asn Thr Lys Val Ala Ser Pro Lys Thr Val <210> 83 <211> 752 <212> DNA
<213> Homo sapiens <400> 83 atgagggtcc ccgctcagct cctggggctc ctgctgctct ggttcccagg ttccagatgc 60 gacatccaga tgacccaatc tccatcttcc gtgtctgcat ctataggaga cagagtctcc 120 atcacttgtc gggcgagtca gggtattagc agctggttag cctggtatca gcagaaacca 180 gggaaagccc ctacgctcct tatctatgct gcatccactt tgcaacgtgg ggtcccatca 240 aggttcagcg gcagtggatc tgggacagat ttcactctca ccatcagcag cctgcagcct 300 gaagattttg caacttactt ttgtcaacag gctaacagtt tcccattcac tttcggccct 360 gggaccaaag tggatatcaa acgaactgtg gctgcaccat ctgtcttcat cttcccgcca 420 tctgatgagc agttgaaatc tggaactgct agcgttgtgt gcctgctgaa taacttctat 480 cccagagagg ccaaagtaca gtggaaggtg gataacgccc tccaatcggg taactcccag 540 gagagtgtca cagagcagga cagcaaggac agcacctaca gcctcagcag caccctgacg 600 ctgagcaaag cagactacga gaaacacaaa gtctacgcct gcgaagtcac ccatcagggc 660 ctgagctcgc ccgtcacaaa gagcttcaac aggggaagtg ggtagtcccg gactcgagcg 720 ggcagtgttt ctcgaagttg tcccctgagt gt 752 <210> 84 <211> 752 <212> DNA
<213> Homo sapiens <400> 84 acactcaggg gacaacttcg agaaacactg cccgctcgag tccgggacta cccacttccc 60 ctgttgaagc tctttgtgac gggcgagctc aggccctgat gggtgacttc gcaggcgtag 120 actttgtgtt tctcgtagtc tgctttgctc agcgtcaggg tgctgctgag gctgtaggtg 180 ctgtccttgc tgtcctgctc tgtgacactc tcctgggagt tacccgattg gagggcgtta 240 tccaccttcc actgtacttt ggcctctctg ggatagaagt tattcagcag gcacacaacg 300 ctagcagttc cagatttcaa ctgctcatca gatggcggga agatgaagac agatggtgca 360 gccacagttc gtttgatatc cactttggtc ccagggccga aagtgaatgg gaaactgtta 420 gcctgttgac aaaagtaagt tgcaaaatct tcaggctgca ggctgctgat ggtgagagtg 480 aaatctgtcc cagatccact gccgctgaac cttgatggga ccccacgttg caaagtggat 540 gcagcataga taaggagcgt aggggctttc cctggtttct gctgatacca ggctaaccag 600 ctgctaatac cctgactcgc ccgacaagtg atggagactc tgtctcctat agatgcagac 660 acggaagatg gagattgggt catctggatg tcgcatctgg aacctgggaa ccagagcagc 720 aggagcccca ggagctgagc ggggaccctc at 752 <210> 85 <211> 234 <212> PRT
<213> Homo sapiens <400> 85 Met Arg Val Pro Ala Gin Leu Leu Gly Leu Leu Leu Leu Trp Phe Pro Gly Ser Arg Cys Asp Ile Gin Met Thr Gin Ser Pro Ser Ser Val Ser Ala Ser Ile Gly Asp Arg Val Ser Ile Thr Cys Arg Ala Ser Gin Gly Ile Ser Ser Trp Leu Ala Trp Tyr Gin Gin Lys Pro Gly Lys Ala Pro Thr Leu Leu Ile Tyr Ala Ala Ser Thr Leu Gin Arg Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Phe Cys Gin Gin Ala Asn Ser Phe Pro Phe Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys Arg Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Giu Gin Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala Lys Val Gin Trp Lys Val Asp Asn Ala Leu Gin Ser 165 k170 175 Gly Asn Ser Gin Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys <210> 86 <211> 1990 <212> DNA
<213> Homo sapiens <400> 86 atgaagcatc tgtggttctt ccttctcctg gtggcagctc ccagatgggt cctttcccag 60 gtgcagctgc aggagtcggg cccaggactg gtgaagcctt cggagaccct gtccctcacc 120 tgcactgtct ctggtgcctc catcagtaat tactactgga gctggatccg gcagccccca 180 gggaagggac tggagtggat tgggtatgtc tcttacagtg ggagtacgta ctaCaacccc 240 tccctcaagg gtcgagtcac catgtcagta gacacgtcca agaaccagtt ctccctgaag 300 ctgagctctg tgaccgctgc ggacacggcc gtgtattact gtgcgagaga aaaactgggg 360 attggagact actggggcca gggaaccctg gtcaccgtct cctcagcctc caccaagggc 420 ccatcggtct tccccctggc gccctgctct agaagcacct ccgagagcac agccgccctg 480 ggctgcctgg tcaaggacta cttccccgaa ccggtgacgg tgtcgtggaa ctcaggcgct 540 ctgaccagcg gcgtgcacac cttcccagct gtcctacagt cctcaggact ctactccctc 600 agcagcgtgg tgaccgtgcc ctccagcaac ttcggcaccc agacciacac ctgcaacgta 660 gatcacaagc ccagcaacac caaggtggac aagacagttg gtgagaggcc agctcaggga 720 gggagggtgt ctgctggaag ccaggctcag ccctcctgcc tggacgcacc ccggctgtgc 780 agccccagcc cagggcagca aggcaggccc catctgtctc ctcacccgga ggcctctgcc 840 cgccccactc atgctcaggg agagggtctt ctggcttttt ccaccaggct ccaggcaggc 900 acaggctggg tgcccctacc ccaggccctt cacacacagg ggcaggtgct tggctcagac 960 ctgccaaaag ccatatccgg gaggaccctg cccctgacct aagccgaccc caaaggccaa 1020 actgtccact ccctcagctc ggacaccttc tctcctccca gatccgagta actcccaatc 1080 ttctctctgc agagcgcaaa tgttgtgtcg agtgcccacc gtgcccaggt aagccagccc 1140 aggcctcgcc ctccagctca aggcgggaca ggtgccctag agtagcctgc atccagggac 1200 aggccccagc tgggtgctga cacgtccacc tccatctctt cctcagcacc acctgtggca 1260 ggaccgtcag tcttcctctt ccccccaaaa cccaaggaca ccctcatgat ctcccggacc 1320 cctgaggtca cgtgcgtggt ggtggacgtg agccacgaag accccgaggt ccagttcaac 1380 tggtacgtgg acggcgtgga ggtgcataat gccaagacaa agccacggga ggagcagttc 1440 aacagcacgt tccgtgtggt cagcgtcctc accgttgtgc accaggactg gctgaacggc 1500 aaggagtaca agtgcaaggt ctccaacaaa ggcctcccag cccccatcga gaaaaccatc 1560 tccaaaacca aaggtgggac ccgcggggta tgagggccac atggacagag gccggctcgg 1620 cccaccctct gccctgggag tgaccgctgt gccaacctct gtccctacag ggcagccccg 1680 agaaccacag gtgtacaccc tgcccccatc ccgggaggag atgaccaaga accaggtcag 1740 cctgacctgc ctggtcaaag gcttctaccc cagcgacatc gccgtggagt gggagagcaa 1800 tgggcagccg gagaacaact acaagaccac acctcccatg ctggactccg acggctcctt 1860 cttcctctac agcaagctca ccgtggacaa gagcaggtgg cagcagggga acgtcttctc 1920 atgctccgtg atgcatgagg ctctgcacaa ccactacacg cagaagagcc tctccctgtc 1980 tccgggtaaa 1990 <210> 87 <211> 1990 <212> DNA
<213> Homo sapiens <400> 87 tttacccgga gacagggaga ggctcttctg cgtgtagtgg ttgtgcagag cctcatgcat 60 cacggagcat gagaagacgt tcccctgctg ccacctgctc ttgtccacgg tgagcttgct 120 gtagaggaag aaggagccgt cggagtccag catgggaggt gtggtcttgt agttgttctc 180 cggctgccca ttgctctccc actccacggc gatgtcgctg gggtagaagc ctttgaccag 240 gcaggtcagg ctgacctggt tcttggtcat ctcctcccgg gatgggggca gggtgtacac 300 ctgtggttct cggggctgcc ctgtagggac agaggttggc acagcggtca ctcccagggc 360 agagggtggg ccgagccggc ctctgtccat gtggccctca taccccgcgg gtcccacctt 420 tggttttgga gatggttttc tcgatggggg ctgggaggcc tttgttggag accttgcact 480 tgtactcctt gccgttcagc cagtcctggt gcacaacggt gaggacgctg accacacgga 540 acgtgctgtt gaactgctcc tcccgtggct ttgtcttggc attatgcacc tccacgccgt 600 ccacgtacca gttgaactgg acctcggggt cttcgtggct cacgtccacc accacgcacg 660 tgacctcagg ggtccgggag atcatgaggg tgtccttggg ttttgggggg aagaggaaga 720 ctgacggtcc tgccacaggt ggtgctgagg aagagatgga ggtggacgtg tcagcaccca 780 gctggggcct gtccctggat gcaggctact ctagggcacc tgtcccgcct tgagctggag 840 ggcgaggcct gggctggctt acctgggcac ggtgggcact cgacacaaca tttgcgctct 900 gcagagagaa gattgggagt tactcggatc tgggaggaga gaaggtgtcc gagctgaggg 960 agtggacagt ttggcctttg gggtcggctt aggtcagggg cagggtcctc ccggatatgg 1020 cttttggcag gtctgagcca agcacctgcc cctgtgtgtg aagggcctgg ggtaggggca 1080 cccagcctgt gcctgcctgg agcctggtgg aaaaagccag aagaccctct ccctgagcat 1140 gagtggggcg ggcagaggcc tccgggtgag gagacagatg gggcctgcct tgctgccctg 1200 ggctggggct gcacagccgg ggtgcgtcca ggcaggaggg ctgagcctgg cttccagcag 1260 acaccctccc tccctgagct ggcctctcac caactgtctt gtccaccttg gtgttgctgg 1320 gcttgtgatc tacgttgcag gtgtaggtct gggtgccgaa gttgctggag ggcacggtca 1380 ccacgctgct gagggagtag agtcctgagg actgtaggac agctgggaag gtgtgcacgc 1440 cgctggtcag agcgcctgag ttccacgaca ccgtcaccgg ttcggggaag tagtccttga 1500 ccaggcagcc cagggcggct gtgctctcgg aggtgcttct agagcagggc gccaggggga 1560 agaccgatgg gcccttggtg gaggctgagg agacggtgac cagggttccc tggccccagt 1620 agtctccaat ccccagtttt tctctcgcac agtaatacac ggccgtgtcc gcagcggtca 1680 cagagctcag cttcagggag aactggttct tggacgtgtc tactgacatg gtgactcgac 1740 ccttgaggga ggggttgtag tacgtactcc cactgtaaga gacataccca atccactcca 1800 gtcccttccc tgggggctgc cggatccagc tccagtagta attactgatg gaggcaccag 1860 agacagtgca ggtgagggac agggtctccg aaggcttcac cagtcctggg cccgactcct 1920 gcagctgcac ctgggacagg acccatctgg gagctgccac caggagaagg aagaaccaca 1980 gatgcttcat 1990 <210> 88 <211> 241 <212> PRT
<213> Homo sapiens <400> 88 Met Lys His Leu Trp Phe Phe Leu Leu Leu Val Ala Leu Ala Ala Pro Arg Trp Val Leu Ser Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Ala Ser Ile Ser Asn Tyr Tyr Trp Ser Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Val Ser Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro Ser Leu Lys Gly Arg Val Thr Met Ser Val Ala Ser Pro Thr Ser Lys Asn Gln Phe Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Glu Lys Leu Gly Ile Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala Leu G1y Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gln Thr Tyr Thr Cys Asn Val Ala Ser Pro His Lys Pro Ser Asn Thr Lys Val Ala Ser Pro Lys Thr Val <210> 89 <211> 702 <212> DNA
<213> Homo sapiens <400> 89 atgaggctcc ccgctcagct cctggggctc ctgctgctct ggttcccagg tgccaggtgt 60 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 120 atcacttgcc gggcaagtca gggcattaaa aatgatttag gctggtatca gcagaaacca 180 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 240 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 300 gaagattttg caacttatta ctgtctacag cataatagtt atccgtgcag ttttggccag 360 gggaccaagc tggagatcaa acgaactgtg gctgcaccat ctgtcttcat cttcccgcca 420 tctgatgagc agttgaaatc tggaactgct agcgttgtgt gcctgctgaa taacttctat 480 cccagagagg ccaaagtaca gtggaaggtg gataacgccc tccaatcggg taactcccag 540 gagagtgtca cagagcagga cagcaaggac agcacctaca gcctcagcag caccctgacg 600 ctgagcaaag cagactacga gaaacacaaa gtctacgcct gcgaagtcac ccatcagggc 660 ctgagctcgc ccgtcacaaa gagcttcaac aggggagagt gt 702 <210> 90 <211> 702 <212> DNA
<213> Homo sapiens <400> 90 acactctccc ctgttgaagc tctttgtgac gggcgagctc aggccctgat gggtgacttc 60 gcaggcgtag actttgtgtt tctcgtagtc tgctttgctc agcgtcaggg tgctgctgag 120 gctgtaggtg ctgtccttgc tgtcctgctc tgtgacactc tcctgggagt tacccgattg 180 gagggcgtta tccaccttcc actgtacttt ggcctctctg ggatagaagt tattcagcag 240 gcacacaacg ctagcagttc cagatttcaa ctgctcatca gatggcggga agatgaagac 300 agatggtgca gccacagttc gtttgatctc cagcttggtc ccctggccaa aactgcacgg 360 ataactatta tgctgtagac agtaataagt tgcaaaatct tcaggctgca ggctgctgat 420 tgtgagagtg aattctgtcc cagatccact gccgctgaac cttgatggga ccccactttg 480 caaactggat gcagcataga tcaggcgctt aggggctttc cctggtttct gctgatacca 540 gcctaaatca tttttaatgc cctgacttgc ccggcaagtg atggtgactc tgtctcctac 600 agatgcagac agggaggatg gagactgggt catctggatg tcacacctgg cacctgggaa 660 ccagagcagc aggagcccca ggagctgagc ggggagcctc at 702 <210> 91 <211> 234 <212> PRT
<213> Homo sapiens <400> 91 Met Arg Leu Pro Ala Gln Leu Leu Gly Leu Leu Leu Leu Trp Phe Pro Gly Ala Arg Cys Asp Ile Gin Met Thr Gin Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gin Gly Ile Lys Asn Asp Leu Gly Trp Tyr Gin Gin Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gin Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gin His Asn Ser Tyr Pro Cys Ser Phe Gly Gin Gly Thr Lys Leu Glu Ile Lys Arg Thr Val Ala Ala Pro Ser Val Phe Ile She Pro Pro Ser Asp Glu Gin Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn She Tyr Pro Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gin Ser Gly Asn Ser Gin Glu Ser Val Thr Glu Gin Asp Ser Lys Asp Ser Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gln Giy Leu Ser Ser Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys <210> 92 <211> 1996 <212> DNA
<213> Homo sapiens <400> 92 atgaaacatc tgtggttctt cctcctgctg gtggcagctc ccagatgggt cctgtcccag 60 gtgcagctgc aggagtcggg cccaggactg gtgaagcctt cacagaccct gtccctcacc 120 tgcactgtct ctggtgcctc catcagcagt ggtgcttaot actggagttg gatccgccag 180 cacccaggga agggcctgga gtggattggg tacatctata agagtgagac ctcctactac 240 aacccgtccc tcaagagtcg acttacccta tcagtagaca cgtctaagaa ccagttctcc 300 ctgaacctga tctctgtgac tgccgcggac acggccgtgt attattgtgc gagagataaa 360 ctggggatcg cggactactg gggccaggga accctggtca ccgtctcctc agcctccacc 420 aagggcccat cggtcttccc cctggcgccc tgctctagaa gcacctccga gagcacagcc 480 gccctgggct gcctggtcaa ggactacttc cccgaaccgg tgacggtgtc gtggaactca 540 ggcgctctga ccaccggcgt gcacaccttc ccagttgtcc tacagtcctc aggactctac 600 tccctcagca gcgtggtgac cgtgccctcc agcaacttcg gcacccagac ctacacctgc 660 aacgtagatc acaagcccag caacaccaag gtggacaaga cagttggtga gaggccagct 720 cagggaggga gggtgtctgc tggaagccag gctcagccct cctgcctgga cgcaccccgg 780 ctgtgcagcc ccagcccagg gcagcaaggc aggccccatc tgtctcctca cccggaggcc 840 tctgcccgcc ccactcatgc tcagggagag ggtcttctgg ctttttccac caggctccag 900 gcaggcacag gctgggtgcc cctaccccag gcccttcaca cacaggggca ggtgcttggc 960 tcagacctgc caaaagccat atccgggagg accctgcccc tgacctaagc cgaccccaaa 1020 ggccaaactg tccactccct cagctcggac accttctctc ctcccagatc cgagtaactc 1080 ccaatcttct ctctgcagag cgcaaatgtt gtgtcgagtg cccaccgtgc ccaggtaagc 1140 cagcccaggc ctcgccctcc agctcaaggc gggacaggtg ccctagagta gcctgcatcc 1200 agggacaggc cccagctggg tgctgacacg tccacctcca tctcttcctc agcaccacct 1260 gtggcaggac cgtcagtctt cctcttcccc ccaaaaccca aggacaccct catgatctcc 1320 cggacccctg aggtcacgtg cgtggtggtg gacgtgagcc acgaagaccc cgaggtccag 1380 ttcaactggt acgtggacgg cgtggaggtg cataatgcca agacaaagcc acgggaggag 1440 cagttcaaca gcacgttccg tgtggtcagc gtcctcaccg ttgtgcacca ggactggctg 1500 aacggcaagg agtacaagtg caaggtctcc aacaaaggcc tcccagcccc catcgagaaa 1560 accatctcca aaaccaaagg tgggacccgc ggggtatgag ggccacatgg acagaggccg 1620 gctcggccca ccctctgccc tgggagtgac cgctgtgcca acctctgtcc ctacagggca 1680 gccccgagaa ccacaggtgt acaccctgcc cccatcccgg gaggagatga ccaagaacca 1740 ggtcagcctg acctgcctgg tcaaaggctt ctaccccagc gacatcgccg tggagtggga 1800 gagcaatggg cagccggaga acaactacaa gaccacacct cccatgctgg actccgacgg 1860 ctccttcttc ctctacagca agctcaccgt ggacaagagc aggtggcagc aggggaacgt 1920 cttctcatgc tccgtgatgc atgaggctct gcacaaccac tacacgcaga agagcctctc 1980 cctgtctccg ggtaaa 1996 <210> 93 <211> 1996 <212> DNA
<213> Homo sapiens <400> 93 tttacccgga gacagggaga ggctcttctg cgtgtagtgg ttgtgcagag cctcatgcat 60 cacggagcat gagaagacgt tcccctgctg ccacctgctc ttgtccacgg tgagcttgct 120 gtagaggaag aaggagccgt cggagtccag catgggaggt gtggtcttgt agttgttctc 180 cggctgccca ttgctctccc actccacggc gatgtcgctg gggtagaagc ctttgaccag 240 gcaggtcagg ctgacctggt tcttggtcat ctcctcccgg gatgggggca gggtgtacac 300 ctgtggttct cggggctgcc ctgtagtgac agaggttggc acagcggtca ctcccagggc 360 agagggtggg ccgagccggc ctctgtccat gtggccctca taccccgcgg gtcccacctt 420 tggttttgga gatggttttc tcgatggggg ctgggaggcc tttgttggag accttgcact 480 tgtactcctt gccgttcagc cagtcctggt gcacaacggt gaggacgctg accacacgga 540 acgtgctgtt gaactgctcc tcccgtggct ttgtcttggc attatgcacc tccacgccgt 600 ccacgtacca gttgaactgg acctcggggt cttcgtggct cacgtccacc accacgcacg 660 tgacctcagg ggtccgggag atcatgaggg tgtccttggg ttttgggggg aagaggaaga 720 ctgacggtcc tgccacaggt ggtgctgagg aagagatgga ggtggacgtg tcagcaccca 780 gctggggcct gtccctggat gcaggctact ctagggcacc tgtcccgcct tgagctggag 840 ggcgaggcct gggctggctt acctgggcac ggtgggcact cgacacaaca tttgcgctct 900 gcagagagaa gattgggagt tactcggatc tgggaggaga gaaggtgtcc gagctgaggg 960 agtggacagt ttggcctttg gggtcggctt agatcagggg cagggtcctc ccggatatgg 1020 cttttggcag gtctgagcca agcacctgcc cctgtgtgtg aagggcctgg ggtaggggca 1080 cccagcctgt gcctgcctgg agcctggtgg aaaaagccag aagaccctct ccctgagcat 1140 gagtggggcg ggcagaggcc tccgggtgag gagacagatg gggcctgcct tgctgccctg 1200 ggttggggct gcacagccgg ggtgcgtcca ggcaggaggg ctgagcctgg cttccagcag 1260 acaccctccc tccctgagct ggcctctcac caactgtctt gtccaccttg gtgttgctgg 1320 gcttgtgatc tacgttgcag gtgtaggtct gggtgccgaa gttgctggag ggcacggtca 1380 ccacgctgct gagggagtag agtcctgagg actgtaggac agctgggaag gtgtgcacgc 1440 cgctggtcag agcgcctgag ttccacgaca ccgtcaccgg ttcggggaag tagtccttga 1500 ccaggcagcc cagggcggct gtgctctcgg aggtgcttct agagcagggc gccaggggga 1560 agaccgatgg gcccttggtg gaggctgagg agacggtgac cagggttccc tggccccagt 1620 agtccgcgat ccccagttta tctctcgcac aataatacac ggccgtgtcc gcggcagtca 1680 cagagatcag gttcagggag aactggttct tagacgtgtc tactgatagg gtaagtcgac 1740 tcttgaggga cgggttgtag taggaggtct cactcttata gatgtaccca atccactcca 1800 ggcccttccc tgggtgctgg cggatccaac tccagtagta agcaccactg ctgatggagg 1860 caccagagac agtgcaggtg agggacaggg tctgtgaagg cttcaccagt cctgggcccg 1920 actcctgcag ctgcacctgg gacaggaccc atctgggagc tgccaccagc aggaggaaga 1980 accacagatg tttcat 1996 <210> 94 <211> 243 <212> PRT
<213> Homo sapiens <400> 94 Met Lys His Leu Trp Phe Phe Leu Leu Leu Val Ala Leu Ala Ala Pro Arg Trp Val Leu Ser Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Gln Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Ala Ser Ile Ser Ser Gly Ala Tyr Tyr Trp Ser Trp Ile Arg Gln His Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Lys Ser Glu Thr Ser Tyr Tyr, Asn Pro Ser Leu Lys Ser Arg Leu Thr Leu Ser Val Ala Ser Pro Thr Sex Lys Asn Gln Phe Ser Leu Asn Leu Ile Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp Lys Leu Gly Ile Ala Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gln Thr Tyr Thr Cys Asn Val Ala Ser Pro His Lys Pro Ser Asn Thr Lys Val Ala Ser Pro Lys Thr Val <210> 95 <211> 702 <212> DNA
<213> Homo sapiens <400> 95 atgagggtcc ccgctcagct cctggggctc ctgctgctct ggttcccagg cgccaggtgt 60 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 120 atcacttgcc gggcaagtca ggacattaga aatgatttag gctggtatca gcagaaacca 180 gggaaagccc ctaagcgcct gatctatgct gcatccaatt tgcaaagtgg ggtcccatca 240 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 300 gaagattttg caacttatta ctgtctacag cataatagct accctcccac tttcggcgga 360' gggaccaagg tggaaatcaa acgaactgtg gctgcaccat ctgtcttcat cttcccgcca 420 tctgatgagc agttgaaatc tggaactgct agcgttgtgt gcctgctgaa taacttctat 480 cccagagagg ccaaagtaca gtggaaggtg gataacgccc tccaatcggg taactcccag 540 gagagtgtca cagagcagga cagcaaggac agcacctaca gcctcagcag caccctgacg 600 ctgagcaaag cagactacga gaaacacaaa gtctacgcct gcgaagtcac ccatcagggc 660 ctgagctcgc ccgtcacaaa gagcttcaac aggggagagt gt 702 <210> 96 <211> 702 <212> DNA
<213> Homo sapiens <400> 96 acactctccc ctgttgaagc tctttgtgac gggcgagctc aggccctgat gggtgacttc 60 gcaggcgtag actttgtgtt tctcgtagtc tgctttgctc agcgtcaggg tgctgctgag 120 gctgtaggtg ctgtccttgc tgtcctgctc tgtgacactc tcctgggagt tacccgattg 180 gagggcgtta tccaccttcc actgtacttt ggcctctctg ggatagaagt tattcagcag 240 gcacacaacg ctagcagttc cagatttcaa ctgctcatca gatggcggga agatgaagac 300 agatggtgca gccacagttc gtttgatttc caccttggtc cctccgccga aagtgggagg 360, gtagctatta tgctgtagac agtaataagt tgcaaaatct tcaggctgca ggctgctgat 420 tgtgagagtg aattctgtcc cagatccact gccgctgaac cttgatggga ccccactttg 480 caaattggat gcagcataga tcaggcgctt aggggctttc cctggtttct gctgatacca 540 gcctaaatca tttctaatgt cctgacttgc ccggcaagtg atggtgactc tgtctcctac 600 agatgcagac agggaggatg gagactgggt catctggatg tcacacctgg cgcctgggaa 660 ccagagcagc aggagcccca ggagctgagc ggggaccctc at 702 <210> 97 <211> 234 <212> PRT
<213> Homo sapiens <400> 97 Met Arg Val Pro Ala Gln Leu Leu Gly Leu Leu Leu Leu Trp Phe Pro Gly Ala Arg Cys Asp Ile Gln Met Thr Gin Ser Pro Ser Sex Leu Ser Ala'Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Asp Ile Arg Asn Asp Leu Gly Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Asn Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Ser Tyr Pro Pro Thr Phe Gly Gly Gly Thr Lys Val Glu Ile Lys Arg Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala Lys Val Gin Trp Lys Val Asp Asn Ala Leu Gln Ser Gly Asn Ser Gln Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys <210> 98 <211> 1990 <212> DNA
<213> Homo sapiens <400> 98 atgaaacacc tgtggttctt ccttctcctg gtggcagctc ccagatgggt cctgtcccag 60 gtgcagctgc aggagtcggg cccaggactg gtgaagcctt cggagaccct gtccctcacc 120 tgcactgtct ctggtgtctc catcagtaat tactactgga gctggatccg gcagtcccca 180 gggaagggac tggagtggat tggatatatc tattacagtg ggagtcccta ttacaacccc 240 tccctcaaga gtcgagtcac tatatctgca gacacgtcca agaaccaatt ctccctgaag 300 ctgagctctg tgaccgctgc ggacacggcc atttattact gtgcgagaga aaaactgggg 360 attggagact actggggcca gggaaccctg gtcaccgtct cctcagcctc caccaagggc 420 ccatcggtct tccccctggc gccctgctct agaagcacct ccgagagcac agccgccctg 480 ggctgcctgg tcaaggacta cttccccgaa ccggtgacgg tgtcgtggaa ctcaggcgct 540 ctgaccagcg gcgtgcacac cttcccagct gtcctacagt cctcaggact ctactccctc 600 agcagcgtgg tgaccgtgcc ctccagcaac ttcggcaccc agacctacac ctgcaacgta 660 gatcacaagc ccagcaacac caaggtggac aagacagttg gtgagaggcc agctcaggga 720 gggagggtgt ctgctggaag ccaggctcag ccctcctgcc tggacgcacc ccggctgtgc 780 agccccagcc cagggcagca aggcaggccc catctgtctc ctcacccgga ggcctctgcc 840 cgccccactc atgctcaggg agagggtctt ctggcttttt ccaccaggct ccaggcaggc 900 acaggctggg tgcccctacc ccaggccctt cacacacagg ggcaggtgct tggctcagac 960 ctgccaaaag ccatatccgg gaggaccctg cccctgacct aagccgaccc caaaggccaa 1020 actgtccact ccctcagctc ggacaccttc tctcctccca gatccgagta actcccaatc 1080 ttctctctgc agagcgcaaa tgttgtgtcg agtgcccacc gtgcccaggt aagccagccc 1140 aggcctcgcc ctccagctca aggcgggaca ggttccctag agtagcctgc atccagggac 1200 aggccccagc tgggtgctga cacgtccacc tccatctctt cctcagcatC acctgtggca 1260 ggaccgtcag tcttcctctt ccccccaaaa cccaaggaca ccctcatgat ctcccggacc 1320 cctgaggtca cgtgcgtggt ggtggacgtg agccacgaag accccgaggt ccagttcaac 1380 tggtacgtgg acggcgtgga ggtgcataat gccaagacaa agccacggga ggagcagttc 1440 aacagcacgt tccgtgtggt cagcgtcctc accgttgtgc accaggactg gctgaacggc 1500 aaggagtaca agtgcaaggt ctccaacaaa ggcctcccag cccccatcga gaaaaccatc 1560 tccaaaacca aaggtgggac ccgcggggta tgagggccac atggacagag gccggctcag 1620 cccaccctct gccctgggag tgaccgctgt gccaacctct gtccctacag ggcagccccg 1680 agaaccacag gtgtacaccc tgcccccatc ccgggaggag atgaccaaga accaggtcag 1740 cctgacctgc ctgctcaaag gcttctaccc cagcgacatc gccgtggagt gggagagcaa 1800 tgggcagccg gagaacaact acaagaccac acctcccatg ctggactccg acggctcctt 1860 cttcctctac agcaagctca ccgtggacaa gagcaggtgg cagcagggga acgtcttctc 1920 atgctccgtg atgcatgagg ctctgcacaa ccactacacg cagaagagcc tctccctgtc 1980 tccgggtaaa 1990 <210> 99 <211> 1990 <212> DNA
<213> Homo sapiens <400> 99 tttacccgga gacagggaga ggctcttctg cgtgtagtgg ttgtgcagag cctcatgcat 60 cacggagcat gagaagacgt tcccctgctg ccacctgctc ttgtccacgg tgagcttgct 120 gtagaggaag aaggagccgt cggagtccag catgggaggt gtggtcttgt agttgttctc 180 cggctgccca ttgctctccc actccacggc gatgtcgctg gggtagaagc ctttgaccag 240 gcaggtcagg ctgacctggt tcttggtcat ctcctcccgg gatgggggca gggtgtacac 300 ctgtggttct cggggctgcc ctgtagggac agaggttggc acagcggtca ctcccagggc 360 agagggtggg ccgagccggc ctctgtccat gtggccctca taccccgcgg gtcccacctt 420 tggttttgga gatggttttc tcgatggggg ctgggaggcc tttgttggag accttgcact 480 tgtactcctt gccgttcagc cagtcctggt gcacaacggt gaggacgctg accacacgga 540 acgtgctgtt gaactgctcc tcccgtagct ttgtcttggc attatgcacc tccacgCcgt 600 ccacgtacca gttgaactgg acctcggggt cttcgtggct cacgtccacc accacgcacg 660 tgacctcagg ggtccgggag atcatgaggg tgtccttggg ttttgggggg aagaggaaga 720 ctgacggtcc tgccacaggt ggtgctgagg aagagatgga ggtggacgtg tcagcaccca 780 gctggggcct gtccctggat gcaggctact ctagggcacc tgtcccgcct tgagctggag 840 ggcgaggcct gggctggctt acctgggcac ggtgggcact cgacacaaca tttgcgctct 900 gcagagagaa gattgggagt tactcggatc tgggaggaga gaaggtgtcc gagctgaggg 960 agtggacagt ttggcctttg gggtcggctt aggtcagggg cagggtcctc ccggatatgg 1020 cttttggcag gtctgagcca agcacctgcc cctgtgtgtg aagggcctgg ggtaggggca 1080 cccagcctgt gcctgcctgg agcctggtgg aaaaagccag aagaccctct ccctgagcat 1140 gagtggggcg ggcagaggcc tccgggggag gagacagatg gggcctgcct tgctgccctg 1200 ggctggggct gcacagccgg ggtgcgtcca ggcaggaggg ctgagcctgg cttccagcag 1260 acaccctccc tccctgagct ggcctctcac caactgtctt gtccaccttg gtgttgctgg 1320 gcttgtgatc tacgttgcag gtgtaggtct gggtgccgaa gttgctggag ggcacggtca 1380 ccacgctgct gagggagtag agtcctgagg actgtaggac agctgggaag gtgtgcacgc 1440 cgctggtcag agcgcctgag ttccacgaca ccgtcaccgg ttcggggaag tagtccttga 1500 ccaggcagcc cagggcggct gtgctctcgg aggtgcttct agagcagggc gccaggggga 1560, agaccgatgg gcccttggtg gaggctgagg agacggtgac cagggttccc tggccccagt 1620 agtctccaat ccccagtttt tctctcgcac agtaataaat ggccgtgtcc gcagcggtca 1680 cagagctcag cttcagggag aattggttct tggacgtgtc tgcagatata gtgactcgac 1740 tcttgaggga ggggttgtaa tagggactcc cactgtaata gatatatcca atccactcca 1800 gtcccttccc tggggactgc cggatccagc tccagtagta attactgatg gagacaccag 1860 agacagtgca ggtgagggac agggtctccg aaggcttcac cagtcctggg cccgactcct 1920 gcagctgcac ctgggacagg acccatctgg gagctgccac caggagaagg aagaaccaca 1980 ggtgtttcat 1990 <210> 100 <211> 239 <212> PRT
<213> Homo sapiens <400> 100 Met Lys His Leu Trp Phe Phe Leu Leu Leu Val Ala Leu Ala Ala Pro Arg Trp Val Leu Ser Gin Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Val Ser Ile Ser Asn Tyr Tyr Trp Ser Trp Ile Arg Gln Ser Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Ile Tyr Tyr Ser Gly Ser Pro Tyr Tyr Asn Pro Ser Leu Lys Ser Arg Val Thr Ile Ser Ala Asp Thr Ser Lys Asn Gln Phe Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Ile Tyr Tyr Cys Ala Arg Glu Lys Leu Gly Ile Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gln Thr Tyr Thr Cys Asn Val Ala Ser Pro His Lys Pro Ser Asn Thr Lys Val Ala Ser Pro Lys Thr Val <210> 101 <211> 702 <212> DNA
<213> Homo sapiens <400> 101 atgagggtcc ccgctcagct cctggggctc ctgctgctct ggttcccagg tgccaggtgt 60 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtcggaga cagagtcacc 120 atcacttgcc gggcaagtca gggcattaga aatgatttag gctggtatca gcagaaacca 180 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 240 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 300 gaagattttg caacttatta ctgtctacag cataatagtt accctcccac tttcggccct 360 gggaccaagg tggatatcaa acgaactgtg gctgcaccat ctgtcttcat cttcccgcca 420 tctgatgagc agttgaaatc tggaactgct agcgttgtgt gcctgctgaa taacttctat 480 cccagagagg ccaaagtaca gtggaaggtg gataacgccc tccaatcggg taactcccag 540 gagagtgtca cagagcagga cagcaaggac agcacctaca gcctcagcag caccctgacg 600 ctgagcaaag cagactacga gaaacacaaa gtctacgcct gcgaagtcac ccatcagggc 660 ctgagctcgc ccgtcacaaa gagcttcaac aggggagagt gt 702 <210> 102 <211> 702 <212> DNA
<213> Homo sapiens <400> 102 acactctccc ctgttgaagc tctttgtgac gggcgagctc aggccctgat gggtgacttc 60 gcaggcgtag actttgtgtt tctcgtagtc tgctttgctc agcgtcaggg tgctgctgag 120 gctgtaggtg ctgtccttgc tgtcctgctc tgtgacactc tcctgggagt tacccgattg 180 gagggcgtta tccaccttcc actgtacttt ggcctctctg ggatagaagt tattcagcag 240 gcacacaacg ctagcagttc cagatttcaa ctgctcatca gatggcggga agatgaagac 300 agatggtgca gccacagttc gtttgatatc caccttggtc ccagggccga aagtgggagg 360 gtaactatta tgctgtagac agtaataagt tgcaaaatct tcaggctgca ggctgctgat 420 tgtgagagtg aattctgtcc cagatccact gccgctgaac cttgatggga ccccactttg 480 caaactggat gcagcataga tcaggcgctt aggggctttc cctggtttct gctgatacca 540 gcctaaatca tttctaatgc cctgacttgc ccggcaagtg atggtgactc tgtctccgac 600 agatgcagac agggaggatg gagactgggt catctggatg tcacacctgg cacctgggaa 660 ccagagcagc aggagcccca ggagctgagc ggggaccctc at 702 <210> 103 <211> 234 <212> PRT
<213> Homo sapiens <400> 103 Met Arg Val Pro Ala Gln Leu Leu Gly Leu Leu Leu Leu Trp Phe Pro Gly Ala Arg Cys Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gln Gly Ile Arg Asn Asp Leu Gly Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gln Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Ser Tyr Pro Pro Thr Phe Gly Pro Gly Thr Lys Val Asp Ile Lys Arg Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gln Ser Gly Asn Ser Gln Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys <210> 104 <211> 1990 <212> DNA
<213> Homo sapiens <400> 104 atgaaacatc tgtggttctt ccttctcctg gtggcagctc ccagatgggt cctgtcccag 60 gtgcagctgc aggagtcggg cccaggactg gtgaagcctt cggagaccct gtccctcacc 120 tgcactgtct ctggtggctc catcagtcgt tactactgga gctggatccg gcagccccca 180 gggaagggac tggagtggat tgggtatgtc tcttacagtg ggagcaccta ctacaacccc 240 tccctcaaga gtcgagtcac catatcagta gacacgtcca agaaccagtt ctccctgaag 300 ctgagctctg tgaccgctgc ggacacggcc gtgtattact gtgcgagaga taaactgggg 360 attggagact actggggcca gggaaccctg gtcaccgtct cctcagcctc caccaagggc 420 ccatcggtct tccccctggc gccctgctct agaagcacct ccgagagcac agccgccctg 480 ggctgcctgg tcaaggacta cttccccgaa ccggtgacgg tgtcgtggaa ctcaggcgct 540 ctgaccagcg gcgtgcacac cttcccagct gtcctacagt cctcaggact ctactccctc 600 agcagcgtgg tgaccgtgcc ctccagcaac ttcggcaccc agacctacac ctgcaacgta 660 gatcacaagc ccagcaacac caaggtggac aagacagttg gtgagaggcc agctcaggga 720 gggagggtgt ctgctggaag ccaggctcag ccctcctgcc tggacgcacc ccggctgtgc 780 agccccagcc cagggcagca aggcaggccc catctgtctc ctcacccgga ggcctctgcc 840 cgccccactc atgctcaggg agagggtctt ctggcttttt ccaccaggct ccaggcaggc 900 acaggctggg tgcccctacc ccaggccctt cacacacagg ggcaggtgct tggctcagac 960 ctgccaaaag ccatatccgg gaggaccctg cccctgacct aagccgaccc caaaggccaa 1020 actgtccact ccctcagctc ggacaccttc tctcctccca gatccgagta actcccaatc 1080 ttctctctgc agagcgcaaa tgttgtgtcg agtgcccacc gtgcccaggt aagccagccc 1140 aggcctcgcc ctccagctca aggcgggaca ggtgccctag agtagcctgc atccagggac 1200 aggccccagc tgggtgctga cacgtccacc tccatctctt cctcagcacc acctgtggca 1260 ggaccgtcag tcttcctctt ccccccaaaa cccaaggaca ccctcatgat ctcccggacc 1320 cctgaggtca cgtgcgtggt ggtggacgtg agccacgaag accccgaggt ccagttcaac 1380 tggtacgtgg acggcgtgga ggtgcataat gccaagacaa agccacggga ggagcagttc 1440 aacagcacgt tccgtgtggt cagcgtcctc accgttgtgc accaggactg gctgaacggc 1500 aaggagtaca agtgcaaggt ctccaacaaa ggcctcccag cccccatcga gaaaaccatc 1560 tccaaaacca aaggtgggac ccgcggggta tgagggccac atggacagag gccggctcgg 1620 cccaccctct gccctgggag tgaccgctgt gccaacctct gtccctacag ggcagccccg 1680 agaaccacag gtgtacaccc tgcccccatc ccgggaggag atgaccaaga accaggtcag 1740 cctgacctgc ctggtcaaag gcttctaccc cagcgacatc gccgtggagt gggagagcaa 1800 tgggcagccg gagaacaact acaagaccac acctcccatg ctggactccg acggctcctt 1860 cttcctctac agcaagctca ccgtggacaa gagcaggtgg cagcagggga acgtcttctc 1920 atgctccgtg atgcatgagg ctctgcacaa ccactacacg cagaagagcc tctccctgtc 1980 tccgggtaaa 1990 <210> 105 <211> 1990 <212> DNA
<213> Homo sapiens <400> 105 tttacccgga gacagggaga ggctcttctg cgtgtagtgg ttgtgcagag cctcatgcat 60 cacggagcat gagaagacgt tcccctgctg ccacctgctc ttgtccacgg tgagcttgct 120 gtagaggaag aaggagccgt cggagtccag catgggaggt gtggtcttgt agttgttctc 180 cggctgccca ttgctctccc actccacggc gatgtcgctg gggtggaaac ctttgaccag 240 gcaggtcagg ctgacctggt tcttggtcat ctcctcccgg gatgggggca gggtgtacac 300 ctgtggttct cggggctgcc ctgtagggac agaggttggc acagcggtca ctcccacggc 360 agagggtggg ccgagccggc ctctgtccat gtggccctca taccccgcgg gtcccacctt 420 tggttttgga gatggttttc tcgatggggg ctgggaggcc tttgttggag accttgcact 480 tgtactcctt gccgttcagc cagtcctggt gcacaacggt gaggacgctg accacacgga 540 acgtgctgtt gaactgctcc tcccgtggct ttgtcttggc attatgcacc tccacgccgt 600 ccacgtacca gttgaactgg acctcggggt cttcgtggct cacgtccacc accacgcacg 660 tgacctcagg ggtccgggag atcatgaggg tgtccttggg ttttgggggg aagaggaaga 720 ctgacggtcc tgccacaggt ggtgctgagg aagagatgga ggtggacgtg tcagcaccca 780 gctggggcct gtccctggat gcaggctact ctagggcacc tgtcccgcct tgagctggag 840 ggcgaggcct gggctggctt acctgggcac ggtgggcact cgacacaaca tttgcgctct 900 gcagagagaa gattgggagt tactcggatc tgggaggaga gaaggtgtcc gagctgaggg 960 agtggacagt ttggcctttg gggtcggctt aggtcagggg cagggtcctc ccggatatgg 1020 cttttggcag gtctgagcca agcacctgcc cctgtgtgtg aagggcctgg ggtaggggca 1080 cccagcctgt gcctgcctgg agcctggtgg aaaaagccag aagaccctct ccctgagcat 1140 gagtggggcg ggcagaggcc tccgggtgag gagacagatg gggcctgcct tgctgccctg 1200 ggctggggct gcacagccgg ggtgcgtcca ggcaggaggg ctgagcctgg cttccagcag 1260 acaccctccc tccctgagct ggcctctcac caactgtctt gtccaccttg gtgttgctgg 1320 gcttgtgatc tacgttgcag gtgtaggtct gggtgccgaa gttgctggag ggcacggtca 1380 ccacgctgct gagggagtag agtcctgagg actgtaggac agctgggaag gtgtgcacgc 1440 cgctggtcag agcgcctgag ttccacgaca ccgtcaccgg ttcggggaag tagtccttga 1500 ccaggcagcc cagggcggct gtgctctcgg aggtgcttct agagcagggc gccaggggga 1560 agaccgatgg gcccttggtg gaggctgagg agacggtgac cagggttccc tggccccagt 1620 agtctccaat ccccagttta tctctcgcac agtaatacac ggccgtgtcc gcagcggtca 1680 cagagctcag cttcagggag aactggttct tggacgtgtc tactgatatg gtgactcgac 1740 tcttgaggga ggggttgtag taggtgctcc cactgtaaga gacataccca atccactcca 1800 gtcccttccc tgggggctgc cggatccagc tccagtagta acgactgatg gagccaccag 1860 agacagtgca ggtgagggac agggtctccg aaggcttcac cagtcctggg cccgactcct 1920 gcagctgcac ctgggacagg acccatctgg gagctgccac caggagaagg aagaaccaca 1980 gatgtttcat 1990 <210> 106 <211> 241 <212> PRT
<213> Homo sapiens <400> 106 Met Lys His Leu Trp Phe Phe Leu Leu Leu Val Ala Leu Ala Ala Pro Arg Trp Val Leu Ser Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Ser Glu Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Gly Ser Ile Ser Arg Tyr Tyr Trp Ser Trp Ile Arg Gln Pro Pro Gly Lys Gly Leu Glu Trp Ile Gly Tyr Val Ser Tyr Ser Gly Ser Thr Tyr Tyr Asn Pro Ser Leu Lys Ser Arg Val Thr Ile Ser Val Ala Ser Pro Thr Ser Lys Asn Gln Phe Ser Leu Lys Leu Ser Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp Lys Leu Gly Ile Gly Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gln Thr Tyr Thr Cys Asn Val Ala Ser Pro His Lys Pro Ser Asn Thr Lys Val Ala Ser Pro Lys Thr Val <210> 107 <211> 702 <212> DNA
<213> Homo sapiens <400> 107 atgaggctcc ctgctcagct cctggggctc ctgctgctct ggttcccagg tgccaggtgt 60 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 120 atcacttgcc gggcaagtca gggcattaga aatgatttag gctggtatca gcagaaaccg 180 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 240 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 300 gaagattttg caacttatta ctgtctacag cataatagtt acccgtgcag ttttggccag 360 gggaccaagc tggagatcaa acgaactgtg gctgcaccat ctgtcttcat cttcccgcca 420 tctgatgagc agttgaaatc tggaactgct agcgttgtgt gcctgctgaa taacttctat 480 cccagagagg ccaaagtaca gtggaaggtg gataacgccc tccaatcggg taactcccag 540 gagagtgtca cagagcagga cagcaaggac agcacctaca gcctcagcag caccctgacg 600 ctgagcaaag cagactacga gaaacacaaa gtctacgcct gcgaagtcac ccatcagggc 660 ctgagctcgc ccgtcacaaa gagcttcaac aggggagagt gt 702 <210> 108 <211> 702 <212> DNA
<213> Homo sapiens <400> 108 acactctccc ctgttgaagc tctttgtgac gggcgagctc aggccctgat gggtgacttc 60 gcaggcgtag actttgtgtt tctcgtagtc tgctttgctc agcgtcaggg tgctgctgag 120 gctgtaggtg ctgtccttgc tgtcctgctc tgtgacactc tcctgggagt tacccgattg 180 gagggcgtta tccaccttcc actgtacttt ggcctctctg ggatagaagt tattcagcag 240 gcacacaacg ctagcagttc cagatttcaa ctgctcatca gatggcggga agatgaagac 300 agatggtgca gccacagttc gtttgatctc cagcttggtc ccctggccaa aactgcacgg 360 gtaactatta tgctgtagac agtaataagt tgcaaaatct tcaggctgca ggctgctgat 420 tgtgagagtg aattctgtcc cagatccact gccgctgaac cttgatggga ccccactttg 480 caaactggat gcagcataga tcaggcgctt aggggctttc cccggtttct gctgatacca 540 gcctaaatca tttctaatgc cctgacttgc ccggcaagtg atggtgactc tgtctcctac 600 agatgcagac agggaggatg gagactgggt catctggatg tcacacctgg cacctgggaa 660 ccagagcagc aggagcccca ggagctgagc agggagcctc at 702 <210> 109 <211> 234 <212> PRT
<213> Homo sapiens <400> 109 Met Arg Leu Pro Ala Gin Leu Leu Gly Leu Leu Leu Leu Trp Phe Pro Gly Ala Arg Cys Asp Ile Gin Met Thr Gin Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Ala Ser Gin Gly Ile Arg Asn Asp Leu Gly Trp Tyr Gin Gin Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gin Ser Gly Val Pro Ser Arg Phe Her Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gin His Asn Ser Tyr Pro Cys Ser Phe Gly Gin Gly Thr Lys Leu Glu Ile Lys Arg Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gin Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala Lys Val Gin Trp Lys Val Asp Asn Ala Leu Gin Ser Gly Asn Ser Gin Glu Ser Val Thr Glu Gin Asp Ser Lys Asp Ser Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gin Gly Leu Ser Ser Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys <210> 110 <211> 1996 <212> DNA
<213> Homo sapiens <400> 110 atgaagcatc tgtggttctt cctcctgctg gtggcagctc ccagatgggt cctgtcccag 60 gtgcagctgc aggagtcggg cccaggactg gtgaagcctt tacagaccct gtccctcacc 120 tgcactgtct ctggtggctc catcagcagt ggtgtttact actggagctg gatccgccag 180 cacccgggga agggcctgga gtggattggg tacatctata acagtaagac ctcctattat 240 aatccgtccc tcaagagtcg acttacccta tcagtagaca cgtctaagaa ccagttctcc 300 ctgaacctga tctctgtgac tgccgcggac acggccgtgt attactgtgc gagagataaa 360 ttggggatcg cggactactg gggccaggga accctggtca ccgtctcctc agcctccacc 420 aagggcccat cggtcttccc cctggcgccc tgctctagaa gcacctccga gagcacagcc 480 gccctgggct gcctggtcaa ggactacttc cccgaaccgg tgacggtgtc gtggaactca 540 ggcgctctga ccagcggcgt gcacaccttc ccagctgtcc tacagtcctc aggactctac 600 tccctcagca gcgtggtgac cgtgccctcc agcaacttcg gcacccagac ctacacctgc 660 aacgtagatc acaagcccag caacaccaag gtggacaaga cagttggtga gaggccagct 720 cagggaggga gggtgtctgc tggaagccag gctcagccct cctgcctgga cgcaccccgg 780 ctgtgcagcc ccagcccagg gcagcaaggc aggccccatc tgtctcctca cccggaggcc 840 tctgcccgcc ccactcatgc tcagggagag ggtcttctgg ctttttccac caggctccag 900 gcaggcacag gctgggtgcc cctaccccag gcccttcaga cacaggggca ggtgcttggc 960 tcagacctgc caaaagccat atccgggagg accctgcccc tgacctaagc cgaccccaaa 1020 ggccaaactg tccactccct cagctcggac accttctctc ctcccagatc cgagtaactc 1080 ccaatcttct ctctgcagag cgcaaatgtt gtgtcgagtg ccaaccgtgc ccaggtaagc 1140 cagcccaggc ctcgccctcc agctcaaggc gggacaggtg ccctagagta gcctgcatcc 1200 agggacaggc cccagctggg tgctgccacg tccacctcca tctcttcctc agcaccacct 1260 gtggcaggac cgtcagtctt cctcttcccc ccaaaaccca aggacaccct catgatctcc 1320 cggacccctg aggtcacgtg cgtggtggtg gacgtgagcc acgaagaccc cgaggtccag 1380 ttcaactggt acgtggacgg cgtggaggtg cataatgcca agacaaagcc acgggaggag 1440 cagttcaaca gcacgttccg tgtggtcagc gtcctcaccg ttgtgcacca ggactggctg 1500 aacggcaagg agtacaagtg caaggtctcc aacaaaggcc tcccagcccc catcgagaaa 1560 accatctcca aaaccaaagg tgggacccgc ggggtatgag ggccacatgg acagaggccg 1620 gctcggccca ccctctgccc tgggagtgac cgctgtgcca acctctgtcc ctacagggca 1680 gccccgagaa ccacaggtgt acaccctgcc cccatcccgg gaggagatga ccaagaacca 1740 ggtcaccctg acctgcctgg tcaaaggctt ctaccccagc gacatcgccg tggagtggga 1800 gagcaatggg cagccggaga acaactacaa gaccacacct cccatgctgg actccgacgg 1860 ctccttcttc ctctacagca agctcaccgt ggacaagagc aggtggcagc aggggaacgt 1920 cttctcatgc tccgtgatgc atgaggctct gcacaaccac tacacgcaga agagcctctc 1980 cctgtctccg ggtaaa 1996 <210> 111 <211> 1996 <212> DNA
<213> Homo sapiens <400> 111 tttacccgga gacagggaga ggctcttctg cgtgtagtgg ttgtgcagag cctcatgcat 60 cacggagcat gagaagacgt tcccctgctg ccacctgctc ttgtccacgg tgagcttgct 120 gtagaggaag aaggagccgt cggagtccag catgggaggt gtggtcttgt agttgttctc 180 cggctgccca ttgctctccc actccacggc gatgtcgctg gggtagaagc ctttgaccag 240 gcaggtcagg ctgacctggt tcttggtcat ctcctcccgg gatgggggca gggtgtacac 300 ctgtggttct cggggctgcc ctgtagggac agaggttggc acagcggtca ctcccagggc 360 agagggtggg ccgagccggc ctctgtccat gtggccctca taccccgcgg gtcccacctt 420 tggttttgga gatggttttc tcgatggggg ctgggaggcc tttgttggag accttgcact 480 tgtactcctt gccgttcagc cagtcctggt gcacaacggt gaggacgctg accacacgga 540 acgtgctgtt gaactgctcc tcccgtggct ttgtcttggc attatgcacc tccacgccgt 600 ccacgtacca gttgaactgg acctcggggt cttcgtggct cacgtccacc accacgcacg 660 tgacctcagg ggtccgggag atcatgaggg tgtccttggg ttttgggggg aagaggaaga 720 ctgacggtcc tgccacaggt ggtgctgagg aagagatgga ggtggacgtg tcagcaccca 780 gctggggcct gtccctggat gcaggctact ctagggcacc tgtcccgcct tgagctggag 840 ggcgaggcct gggctggctt acctgggcac ggtgggcact cgacacaaca tttgcgctct 900 gcagagagaa gattgggagt tactcggatc tgggaggaga gaaggtgtcc gagctgaggg 960 agtggacagt ttggcctttg gggtcggctt aggtcagggg cagggtcctc ccggatatgg 1020 cttttggcag gtctgagcca agcacctgcc cctgtgtgtg aagggcctgg ggtaggggca 1080 cccagcctgt gcctgcctgg agcctggtgg aaaaagccag aagaccctct ccctgagcat 1140 gagtggggcg ggcagaggcc tccgggtgag gagacagatg gggcctgcct tgctgccctg 1200 ggctggggct gcacagccgg ggtgcgtcca ggcaggaggg ctgagcctgg cttccagcag 1260 acaccctccc tccctgagct ggcctctcac caactgtctt gtccaccttg gtgttgctgg 1320 gcttgtgatc tacgttgcag gtgtaggtct gggtgccgaa gttgctggag ggcacggtca 1380 ccacgctgct gagggagtag agtcctgagg actgtaggac agctgggaag gtgtgcacgc 1440 cgctggtcag agcgcctgag ttccacgaca ccgtcaccgg ttcggggaag tagtccttga 1500 ccaggcagcc cagggcggct gtgctctcgg aggtgcttct agagcagggc gccaggggga 1560 agaccgatgg gcccttggtg gaggctgagg agacggtgac cagggttccc tggccccagt 1620 agtccgcgat ccccaattta tctctcgcac agtaatacac ggccgtgtcc gcggcagtca 1680 cagagatcag gttcagggag aactggttct tagacgtgtc tactgatagg gtaagtcgac 1740 tcttgaggga cggattataa taggaggtct tactgttata gatgtaccca atccactcca 1800 ggcccttccc tgggtgctgg cggatccagc tccagtagta aacaccactg ctgatggagc 1860 caccagagac agtgcaggtg agggacaggg tctgtaaagg cttcaccagt cctgggcccg 1920 actcctgcag ctgcacctgg gacaggaccc atctgggagc tgccaccagc aggaggaaga 1980 accacagatg cttcat 1996 <210> 112 <211> 235 <212> PRT
<213> homo sapiens <400> 112 Met Lys His Leu Trp Phe Phe Leu Leu Leu Val Ala Ala Pro Arg Trp Val Leu Ser Gln Val Gln Leu Gln Glu Ser Gly Pro Gly Leu Val Lys Pro Leu Gln Thr Leu Ser Leu Thr Cys Thr Val Ser Gly Gly Ser Ile Ser Ser Gly Val Tyr Tyr Trp Ser Trp Ile Arg Gln His Pro Gly Lys G1y Leu Glu Trp Ile Gly Tyr Ile Tyr Asn Ser Lys Thr Ser Tyr Tyr Asn Pro Ser Leu Lys Ser Arg Leu Thr Leu Ser Val Asp Thr Ser Lys Asn Gln Phe Ser Leu Asn Leu Ile Ser Val Thr Ala Ala Asp Thr Ala Val Tyr Tyr Cys Ala Arg Asp Lys Leu Gly Ile Ala Asp Tyr Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala ,Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Asn Phe Gly Thr Gln Thr Tyr Thr Cys Asn Val Asp His Lys Pro Ser Asn Thr Lys Val Asp Lys Thr Val <210> 113 <211> 702 <212> DNA
<213> Homo sapiens <400> 113 atgagggtcc ctgctcagct cctggggctc ctgctgctct ggttcccagg tgccaggtgt 60 gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 120 atcacttgcc ggacaagtca gggcattaga aatgatttag gctggtatca gcagaaacca 180 gggaaagccc ctaagcgcct gatctatgct gcatccagtt tgcaaagtgg ggtcccatca 240 aggttcagcg gcagtggatc tgggacagaa ttcactctca caatcagcag cctgcagcct 300 gaagattttg caacttatta ctgtctacag cataatagct accctcccac tttcggcgga 360 gggaccaagg tggagatcaa acgaactgtg gctgcaccat ctgtcttcat cttcccgcca 420 tctgatgagc agttgaaatc tggaactgct agcgttgtgt gcctgctgaa taacttctat 480 cccagagagg ccaaagtaca gtggaaggtg gataacgccc tccaatcggg taactcccag 540 gagagtgtca cagagcagga cagcaaggac agcacctaca gcctcagcag caccctgacg 600 ctgagcaaag cagactacga gaaacacaaa gtctacgcct gcgaagtcac ccatcagggc 660 ctgagctcgc ccgtcacaaa gagcttcaac aggggagagt gt 702 <210> 114 <211> 702 <212> DNA
<213> Homo sapiens <400> 114 acactctccc ctgttgaagc tctttgtgac gggcgagctc aggccctgat gggtgacttc 60 gcaggcgtag actttgtgtt tctcgtagtc tgctttgctc agcgtcaggg tgctgctgag 120 gctgtaggtg ctgtccttgc tgtcctgctc tgtgacactc tcctgggagt,tacccgattg 180 gagggcgtta tccaccttcc actgtacttt ggcctctctg ggatagaagt tattcagcag 240 gcacacaacg ctagcagttc cagatttcaa ctgctcatca gatggcggga agatgaagac 300 agatggtgca gccacagttc gtttgatctc caccttggtc cctccgccga aagtgggagg 360 gtagctatta tgctgtagac agtaataagt tgcaaaatct tcaggctgca ggctgctgat 420 tgtgagagtg aattctgtcc cagatccact gccgctgaac cttgatggga ccccactttg 480 caaactggat gcagcataga tcaggcgctt aggggctttc cctggtttct gctgatacca 540 gcctaaatca tttctaatgc cctgacttgt ccggcaagtg atggtgactc tgtctcctac 600 agatgcagac agggaggatg gagactgggt catctggatg tcacacctgg cacctgggaa 660 ccagagcagc aggagcccca ggagctgagc agggaccctc at 702 <210> 115 <211> 234 <212> PRT
<213> Homo sapiens <400> 115 Met Arg Val Pro Ala Gin Leu Leu Gly Leu Leu Leu Leu Trp Phe Pro Gly Ala Arg Cys Asp Ile Gln Met Thr Gin Ser Pro Ser Ser Leu Ser Ala Ser Val Gly Asp Arg Val Thr Ile Thr Cys Arg Thr Ser Gln Gly Ile Arg Asn Asp Leu Gly Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Arg Leu Ile Tyr Ala Ala Ser Ser Leu Gin Ser Gly Val Pro Ser Arg Phe Ser Gly Ser Gly Ser Gly Thr Glu Phe Thr Leu Thr Ile Ser Ser Leu Gln Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Leu Gln His Asn Ser Tyr Pro Pro Thr Phe Gly Gly Gly Thr Lys Val Glu Ile Lys Arg Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gin Ser Gly Asn Ser Gin Glu Ser Val Thr Glu Gin Asp Ser Lys Asp Ser Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gin Gly Leu Ser Ser Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys

Claims (10)

WHAT IS CLAIMED IS:

1. An isolated antibody or an antigen-binding fragment thereof that activates an endogenous activity of a human erythropoietin receptor in a mammal, comprising:
a heavy chain variable region or an antigen-binding fragment thereof comprising the amino acid sequence of SEQ ID NO: 3; and a light chain variable region or an antigen-binding fragment thereof comprising the amino acid sequence of SEQ I DNO: 5, wherein the antibody or the antigen-binding fragment thereof does not interact with a peptide having an amino acid sequence of SEQ ID NO: 1.

2. An isolated antibody or antigen-binding fragment thereof that activates an endogenous activity of a human erythropoietin receptor in a mammal, the antibody comprising:
a heavy chain variable region or antigen-binding fragment thereof comprising the amino acid sequence of SEQ ID NO: 51; and a light chain variable region or antigen-binding fragment thereof comprising the amino acid sequence of SEQ ID NO: 53, wherein said antibody or antigen-binding fragment thereof does not interact with a peptide having an amino acid sequence of SEQ ID NO: 1.

3. An isolated antibody or an antigen-binding fragment thereof capable of binding to a human erythropoietin receptor in a mammal and comprising at least one heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 3 and at least one light chain variable region comprising the amino acid sequence of SEQ ID NO: 5.

4. An isolated antibody or an antigen-binding fragment thereof capable of binding to a human erythropoietin receptor in a mammal and comprising at least one heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 51 and at least one light chain variable region comprising the amino acid sequence of SEQ ID NO: 53.

5. An isolated antibody or an antigen-binding fragment thereof capable of binding a human erythropoietin receptor in a mammal, said antibody comprising a heavy chain variable region comprising a continuous sequence from CDR1 through CDR3 comprising the amino acid sequence of SEQ ID No: 58 and a light chain variable region comprising a continuous sequence from CDRl through CDR3 comprising the amino acid sequence of SEQ ID
NO: 62.

6. An isolated antibody or an antigen-binding fragment thereof that activates an endogenous activity of a human erythropoietin receptor in a mammal wherein said antibody is Ab12, wherein Ab12 has ATCC Accession No. PTA-5554.

7. Use of the antibody or the antigen-binding fragment thereof of claim 1, 2, 5, or 6 for manufacturing a medicament for activating an endogenous activity of a human erythropoietin receptor in a mammal by administration to the mammal of a therapeutically effective amount to activate the receptor.

8. A pharmaceutical composition comprising the antibody or the antigen-binding fragment of claim 1, 2, 5, or 6, and a carrier.

9. A pharmaceutical composition for treating a mammal suffering at least one of aplasia or anemia, the composition comprising the antibody or the antigen-binding fragment of claim 1, 2, 5, or 6, and a carrier.

10. The pharmaceutical composition of claim 8 or 9 comprising a therapeutically effective amount of at least one of the antibody or the antigen-binding fragment and a pharmaceutically acceptable excipient.