CN118460650A - A preparation method of Nedosiran - Google Patents

Abstract

The present invention provides a method for preparing Nedosiran. Nedosiran is a double-stranded RNA composed of a sense strand and an antisense strand through complementary pairing; the preparation method comprises: mixing a sense strand substrate fragment, an antisense strand substrate fragment and an RNA ligase, wherein the sense strand substrate fragment can form a sense strand, and the antisense strand substrate fragment can form an antisense strand; the sense strand substrate fragment and the antisense strand substrate fragment are connected by hydrogen bonds formed by base complementarity, and the head and tail bases of the sense strand substrate fragment and the antisense strand substrate fragment are not connected to each other, forming a double-stranded nucleotide structure containing a nick; and using RNA ligase to connect the bases at both ends of the nick with a phosphodiester bond to form Nedosiran. The method can solve the problem of low purity of Nedosiran prepared in the prior art, and is applicable to the field of drug biosynthesis technology.

Description

A preparation method of Nedosiran

Technical Field

The present invention relates to the field of drug biosynthesis, and in particular to a method for preparing Nedosiran.

Background Art

In the prior art, diseases caused by gene expression and mutation cannot be cured by traditional small molecule drugs, and such diseases can only be treated by gene expression intervention. siRNA is a double-stranded RNA oligonucleotide with a length of 19-25nt, which can specifically bind to the mRNA of the same target gene, and by blocking the translation process, it can achieve the effect of hindering the expression of the target gene, that is, by mediating RNA interference to cause gene silencing. The research and development of siRNA drugs has brought huge development prospects to gene therapy, and has been widely used in the field of disease treatment. siRNA acts on mRNA, and the druggable target is significantly larger than that of traditional small molecule drugs whose action sites are proteins, and it can act on new targets by changing the sequence. Intervene in gene expression.

Nedosiran is a gene-targeted siRNA double-stranded RNA drug developed by Dicerna for the treatment of primary hyperoxaluria (PH). Nedosiran is indicated for three types of primary hyperoxaluria (PH1, PH2, PH3), and is currently the only drug under development that can treat three types of PH at the same time.

The synthesis method of Nedosiran mainly uses a chemical solid phase synthesis method for preparation. In the synthesis method, a solid phase carrier is used, and the synthesis is cyclically performed by the phosphoramidite triester method. After the synthesis cycle is completed, the Nedosiran chain is cut off from the solid phase carrier by aminolysis, and then purified to obtain the target product. The yield of the product synthesis in this preparation method decreases with the increase of the synthesis chain length. The impurities generated in the synthesis process, such as impurities with one more nucleotide than the target sequence (N+1 impurities) or impurities with one less nucleotide than the target sequence (N-1 impurities), will also increase with the increase of the synthesis chain length. It is not easy to remove, resulting in a complex purification process and low efficiency. As Nedosiran is increasingly widely used in the treatment of primary hyperbilirubinemia, its synthesis scale is limited by the limitations of the synthesis instrument, the cost is high, and it is difficult to scale up production. Therefore, it is necessary to develop a more efficient Nedosiran synthesis method.

Summary of the invention

The main purpose of the present invention is to provide a method for preparing Nedosiran to solve the problem of low purity of Nedosiran prepared in the prior art.

In order to achieve the above object, according to the first aspect of the present invention, a method for preparing Nedosiran is provided, wherein Nedosiran is a double-stranded siRNA consisting of a complementary sense strand and an antisense strand; the preparation method comprises:

The sense strand substrate fragment, the antisense strand substrate fragment and the RNA ligase are mixed, wherein the sense strand substrate fragment can form a sense strand, and the antisense strand substrate fragment can form an antisense strand; the sense strand substrate fragment and the antisense strand substrate fragment are connected by hydrogen bonds formed by base complementarity, and the head and tail bases of the sense strand substrate fragment and the antisense strand substrate fragment are not connected to each other, so as to form a double-stranded nucleotide structure containing a nick; the bases at both ends of the nick are connected by a phosphodiester bond using RNA ligase to form Nedosiran; the bases at both ends of the nick are the 5' end and the 3' end of different substrate fragments, respectively, the 5' end is a phosphate group, and the 3' end is a hydroxyl group; the phosphate group at the 5' end and the hydroxyl group at the 3' end upstream and downstream of the nick are connected by RNA ligase to form a phosphodiester bond to obtain Nedosiran; the RNA ligase is an RNA ligase having an amino acid sequence shown in SEQ ID NO: 1; or an enzyme having more than 70% identity with the RNA ligase shown in SEQ ID NO: 1 and having activity of catalyzing the formation of phosphodiester bonds.

Furthermore, the nucleotide sequence of the sense strand is the nucleotide sequence shown in SEQ ID NO: 19, and the nucleotide sequence of the antisense strand is the nucleotide sequence shown in SEQ ID NO: 20.

Further, the sense strand substrate fragment includes 2 or more strands, and the antisense strand substrate fragment includes 2 or more strands; preferably, the length of the sense strand substrate fragment is 2-34 nt, more preferably 6-30 nt; preferably, the length of the antisense strand substrate fragment is 2-20 nt, more preferably 6-16 nt.

Further, the sense strand substrate fragment and the antisense strand substrate fragment each include 2 strands, the sense strand substrate fragment includes the first sense strand substrate fragment and the second sense strand substrate fragment, and the antisense strand substrate fragment includes the first antisense strand substrate fragment and the second antisense strand substrate fragment. The preparation method includes: mixing the first sense strand substrate fragment, the second sense strand substrate fragment, the first antisense strand substrate fragment and the second antisense strand substrate fragment, under the catalytic action of RNA ligase, the first sense strand substrate fragment and the second sense strand substrate fragment are connected to form a sense strand, catalyzing the connection of the first antisense strand substrate fragment and the second antisense strand substrate fragment to form an antisense strand, and the sense strand and the antisense strand are formed by base complementary pairing to form Nedosiran; preferably, the sense strand substrate fragment and the antisense strand substrate fragment are annealed and then mixed with RNA ligase to obtain Nedosiran.

Further, the nucleotide sequence of the first sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 5, and the nucleotide sequence of the second sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 6; the nucleotide sequence of the first antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 8, and the nucleotide sequence of the second antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 7; preferably, the nucleotide sequence of the first sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 9, and the nucleotide sequence of the second sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 10; the nucleotide sequence of the first antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 12, and the nucleotide sequence of the second antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 11.

Further, the 3' end of the first sense chain substrate fragment and the 5' end of the second sense chain substrate fragment are connected under the catalysis of RNA ligase to form a sense chain; the 3' end of the first antisense chain substrate fragment and the 5' end of the second antisense chain substrate fragment are connected under the catalysis of RNA ligase to form an antisense chain; preferably, the 5' end of the first sense chain substrate fragment is a hydroxyl group, and the 3' end is a hydroxyl group; the 5' end of the second sense chain substrate fragment is a phosphate group, and the 3' end is an R group; preferably, the 5' end of the first antisense chain substrate fragment is a hydroxyl group, and the 3' end is a hydroxyl group; the 5' end of the second antisense chain substrate fragment is a phosphate group, and the 3' end is a hydroxyl group.

Furthermore, the sense chain substrate fragment and the antisense chain substrate fragment each include 3, the sense chain substrate fragment includes a first sense chain substrate fragment, a second sense chain substrate fragment and a third sense chain substrate fragment; the antisense chain substrate fragment includes a first antisense chain substrate fragment, a second antisense chain substrate fragment and a third antisense chain substrate fragment; preferably, the preparation method includes: mixing the first sense chain substrate fragment, the second sense chain substrate fragment, the third sense chain substrate fragment, the first antisense chain substrate fragment, the second antisense chain substrate fragment and the third antisense chain substrate fragment, under the catalytic action of RNA ligase, connecting the first sense chain substrate fragment, the second sense chain substrate fragment and the third sense chain substrate fragment to form a sense chain, catalyzing the connection of the first antisense chain substrate fragment, the second antisense chain substrate fragment and the third antisense chain substrate fragment to form an antisense chain, and the sense chain and the antisense chain form Nedosiran through base complementary pairing; preferably, the sense chain substrate fragment and the antisense chain substrate fragment are annealed and then mixed with RNA ligase to obtain Nedosiran.

Further, the nucleotide sequence of the first sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 13; the nucleotide sequence of the second sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 14; the nucleotide sequence of the third sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 15; preferably, the nucleotide sequence of the first antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 18; the nucleotide sequence of the second antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 17; the nucleotide sequence of the third antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 16.

Furthermore, the concentrations of the sense strand substrate fragment and the antisense strand substrate fragment are independently selected from 0.1-4.5 mM; preferably, the reaction system formed by mixing the sense strand substrate fragment, the antisense strand substrate fragment and the RNA ligase also includes ATP, Tris-HCl, MgCl ₂ and DTT; preferably, the reaction temperature of the preparation method is 10-40°C, more preferably 15-30°C; preferably, the reaction time of the preparation method is 2-48h, more preferably 12-24h.

By applying the technical solution of the present invention and utilizing the above-mentioned preparation method, under the catalysis of RNA ligase, the sense strand substrate fragments are connected to form the Nedosiran sense strand, and the antisense strand substrate fragments are connected to form the Nedosiran antisense strand, thereby realizing the preparation of such siRNA drugs by biosynthesis. Compared with the method for preparing Nedosiran by chemical synthesis, the product obtained by the preparation method of the present application has high purity, less impurities, a simple preparation process, mild reaction conditions, low organic reagent dosage, reduced production costs, and is easy to achieve scale-up industrial production.

BRIEF DESCRIPTION OF THE DRAWINGS

The drawings constituting a part of the present application are used to provide a further understanding of the present invention. The exemplary embodiments of the present invention and their descriptions are used to explain the present invention and do not constitute an improper limitation of the present invention. In the drawings:

FIG. 1 shows a schematic diagram of an enzyme-catalyzed ligation reaction according to Example 1 of the present invention.

FIG. 2 shows a diagram of the R-group structure according to an embodiment of the present invention.

FIG. 3 shows the electrophoresis results of the catalytic products of RNA ligases Ligase25 and Ligase11 according to Example 1 of the present invention.

FIG. 4 shows a graph showing the HPLC detection result of the product catalyzed by RNA ligase Ligase 25 according to Example 2 of the present invention.

FIG. 5 shows the LC-MS detection result of the product catalyzed by RNA ligase Ligase 25 according to Example 2 of the present invention.

DETAILED DESCRIPTION

It should be noted that, in the absence of conflict, the embodiments and features in the embodiments of the present application can be combined with each other. The present invention will be described in detail below in conjunction with the embodiments.

Terminology explanation:

N+1 impurity: A nucleic acid impurity that has a single nucleotide extra attached compared to the target synthetic sequence.

N-1 impurity: A nucleic acid impurity that has a single nucleotide missing compared to the target synthetic sequence.

As mentioned in the background technology, the prior art uses a chemical synthesis method for the preparation of Nedosiran, which is not only complicated and costly, but also produces a large number of N+1 and N-1 impurities, which affect the subsequent purification of the product. In this application, the inventor attempts to develop a method for preparing Nedosiran, using enzyme-catalyzed synthesis to prepare Nedosiran, and thus proposes a series of protection schemes of this application.

In a first typical embodiment of the present application, a method for preparing Nedosiran is provided, wherein Nedosiran is a double-stranded siRNA composed of a complementary sense strand and an antisense strand; the preparation method comprises: mixing a sense strand substrate fragment, an antisense strand substrate fragment and an RNA ligase, wherein the sense strand substrate fragment can form a sense strand, and the antisense strand substrate fragment can form an antisense strand; the sense strand substrate fragment and the antisense strand substrate fragment are connected by hydrogen bonds formed by base complementarity, and the head and tail bases of the sense strand substrate fragment and the antisense strand substrate fragment are not connected to each other, so as to form a double-stranded nucleotide structure containing a nick; using RNA ligase to connect the bases at both ends of the nick by phosphodiester bonds to form Nedosiran; the bases at both ends of the nick are the 5' end and the 3' end of different substrate fragments, respectively, the 5' end is a phosphate group, and the 3' end is a hydroxyl group; using RNA ligase to connect the phosphate group at the 5' end and the hydroxyl group at the 3' end upstream and downstream of the nick to form a phosphodiester bond to obtain Nedosiran; the RNA ligase is a polypeptide having SEQ ID An RNA ligase having the amino acid sequence shown in SEQ ID NO: 1; or an enzyme having 70% or more identity with the RNA ligase shown in SEQ ID NO: 1 and having activity of catalyzing the formation of phosphodiester bonds.

In the above preparation method, the sense strand substrate fragment is a nucleotide sequence that can form two or more sense strands, that is, multiple nucleotide sequences of the sense strand substrate fragment can be spliced to form a sequence identical to the sense strand sequence, and the difference from the sense strand is that there are nicks between the sense strand substrate fragments and they are not connected by phosphodiester bonds. Similarly, the antisense strand substrate fragment and the antisense strand have the above characteristics. Two or more sense strand substrate fragments or antisense strand substrate fragments are connected by phosphodiester bonds using RNA ligase to obtain the sense strand and antisense strand of Nedosiran.

In the above-mentioned preparation method, the sense strand substrate fragment and the antisense strand substrate fragment are mixed with RNA ligase to prepare Nedosiran. In this preparation method, the sense strand substrate fragment and the antisense strand substrate fragment can be complementary paired to form a double-stranded nucleotide structure containing a sticky end, and after forming the sticky end, they continue to bind to other substrates to form a double-stranded nucleotide structure containing a nick. RNA ligase can recognize the nick of this double-stranded structure and connect the nick with a phosphodiester bond, thereby preparing the target product Nedosiran; preferably, the sense strand substrate fragment and the antisense strand substrate fragment are annealed and mixed with RNA ligase to obtain Nedosiran.

In the above preparation method, the sense strand substrate fragment and the antisense strand substrate fragment can be mixed and annealed first, and the sense strand substrate fragment and the antisense strand substrate fragment can form a double-stranded RNA structure through base complementary pairing, and there are nicks between different substrate fragments in the double-stranded RNA structure. Then, the annealed reaction system is mixed with RNA ligase, and the RNA ligase is used to connect the phosphate groups and hydroxyl groups on both sides of the nick with phosphodiester bonds to repair the nick, thereby obtaining the target product Nedosiran with a complete double-stranded structure.

In a preferred embodiment, the nucleotide sequence of the sense strand is the nucleotide sequence shown in SEQ ID NO: 19, and the nucleotide sequence of the antisense strand is the nucleotide sequence shown in SEQ ID NO: 20.

SEQ ID NO: 19:

AmsUmGfUmUfGmUmCfCfUfUfUmUfUmAfUmCfUmGmAmGmCmAmGmCmCmGm*Am*Am*Am*GmGmCmUmGmCm.

SEQ ID NO: 20:

U*sCfsAfsGmAfUmAfAmAfAfAmGmGmAfCmAfAmCfAmUmsGmsGm.

In the present application, m after A, C, G or U indicates 2' methoxy modification of the ribonucleotide, f indicates 2' fluorine modification of the ribonucleotide, s before the ribonucleotide in "sUm", "sAf" and the like indicates thio modification of the 5' phosphate of the ribonucleotide, and * indicates 2' modification with R group. The structure of R group is shown in Figure 2.

In a preferred embodiment, the sense chain substrate fragment includes 2 or more substrate fragments, and the antisense chain substrate includes 2 or more substrate fragments; preferably, the length of the sense chain substrate fragment is 2-34nt, more preferably 6-30nt; preferably, the length of the antisense chain substrate fragment is 2-20nt, more preferably 6-16nt.

Preferably, for the sense strand substrate fragment used to form the 3' end of the sense strand, the length of the sense strand substrate fragment is ≥18 nt, including but not limited to 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31 and 32 nt. The 3' end sense strand substrate fragment of this length can be complementary paired with other substrate fragments to form a secondary structure with a nick, which is convenient for RNA ligase to act and prepare the target product Nedosiran.

In a preferred embodiment, the RNA ligase is an RNA ligase having an amino acid sequence as shown in SEQ ID NO: 1; or an enzyme having more than 70% identity with the RNA ligase shown in SEQ ID NO: 1, including but not limited to 75%, 80%, 85%, 90%, 95%, 99% or more (such as 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 98.5%, 99%, 99.5%, 99.6%, 99.7%, 99.8% or more, or even 99.9% or more) and having activity of catalyzing phosphodiester bond formation.

The above-mentioned RNA ligases are all able to recognize the double-stranded structure with nicks formed by complementary pairing of substrate fragments, thereby catalyzing the formation of phosphodiester bonds between phosphate groups and hydroxyl groups.

SEQ ID NO: 1 (Ligase 25, Vibrio phage NT-1):

MSFVKYTSLENSYRQAFVDKCDMLGVRDWVALEKIHGANFSFIVEFDGGYTVTPAKRTSIIGATATGDYDFYGCTSVVEAHKEKVELVANFLWLNEYINLYEPIIIYGELAGKGIQKEVNYGDKDFWAFDIFLPQREEFVDWDTCVAAFTNAEIKYTKELARGTLDELLRIDPLFKSLHTPAEHEGDNVAEGFVVKQLHSE KRLQSGSRAILKVKNEKFKEKKKKEGKTPTKLVLTPEQEKLHAEFSCYLTENRLKNVLSKLGTVNQKQFGMISGLFVKDAKDEFERDELNEVAIDRDDWNAIRRSLTNIANEILRKNWLNILDGNF.

SEQ ID NO: 2: (Ligase 11, Thermococcus):

MVSSYFRNLLLKLGLPEERLEVLEGKGALAEDEFEGIRYVRFRDSARNFRRGTVVFETGEAVLGFPHIKRVVQLENGIRRVFKNKPFYVEEKVDGYNVRVVKVKDKILAITRGGFVCPFTTERIEDFVNFDFFKDYPNLVLVGEMAGPESPYLVEGPPYVKEDIEFFLFDIQEKGTGRSLPAEERYRLAEEYGIPQVERFGLYDSSKV GELKELIEWLSEEKREGIVMKSPDMRRIAKYVTPYANINDIKIGSHIFFDLPHGYFMGRIKRLAFYLAENHVRGEEFENYAKALGTALLRPFVESIHEVANGGEVDETFTVRVKNITTAHKMVTHFERLGVKIHIEDIEDLGNGYWRITFKRVYPDATREIRELWNGLAFVD.

SEQ ID NO: 3: (Ligase 20, Archaea):

MVVPLKRIDKIRWEIPKFDKRMRVPGRVYADEVLLEKMKNDRTLEQATNVAMLPGIYKYSIVMPDGHQGYGFPIGGVAAFDVKEGVISPGGIGYDINCGVRLIRTNLTEKEVRPRIKQLVDTLFKNVPSGVGSQGRIKLHWTQIDDVLVDGAKWAVDNGYGWERDLERLEEGGRMEGADPEAVSQRAKQRGAPQLGSLGS GNHFLEVQVVDKIFDPEVAKAYGLFEGQVVVMVHTGSRGLGHQV ASDYLRIMERAIRKYRIPWPDRELLVSVPFQSEEGQRYFSAMKAAANFAWANRQMITHWVRESFQEVFKQDPEGDLGMDIVYDVAHNIGKVEEHEVDGKRVKVIVHRKGATRAFPPGHEAVPRLYRDVGQPVLIPGSMGTASYILAGTEGAMKETFGSTCHGAGRVLSRKAATRQYRGDRIRQELLNRGIYVRAASMRVVAEEAPGAYK NVDNVVKVVSEAGIAKLVARMRPIGVAKGAAALEH.

SEQ ID NO: 4: (Ligase 32, bacteria):

MVSLHFKHILLKLGLDKERIEILEMKGGIVEDEFEGLRYLRFKDSAKGLRRGTVVFNESDIILGFPHIKRVVHLRNGVKRIFKSKPFYVEEKVDGYNVRVAKVGEKILALTRGGFVCPFTTERIGDFINEQFFKDHPNLILCGEMAGPESPYLVEGPPYVEEDIQFFLFDIQEKRTGRSIPVEERIKLAEEYGIQSVEIFGLYSYEKIDE LYELIERLSKEGREGVVMKSPDMKKIVKYVTPYANVNDIKIGSRIFFDLPHGYFMQRIKRLAFYIAEKRIRREDFDEYAKALGKALLQPFVESIWDVAAGEMIAEIFTVRVKKIETAYKMVSHFERMGLNIHIDDIEELGNGYWKITFKRVYDDATKEIRELWNGHAFVD.

Identity in this application refers to the "identity" between amino acid sequences or nucleotide sequences, that is, the total ratio of the same type of amino acid residues or nucleotides in the amino acid sequence or nucleotide sequence. The identity of amino acid sequences or nucleotide sequences can be determined using alignment programs such as BLAST (Basic Local Alignment Search Tool) and FASTA.

Proteins with 70%, 75%, 80%, 85%, 90%, 95%, or more than 99% (for example, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 98.5%, 99%, 99.5%, 99.6%, 99.7%, 99.8% or more, or even 99.9% or more) identity and the same function, their active sites, active pockets, active mechanisms, protein structures, etc. are likely to be the same as the proteins provided by the above sequences.

As used herein, the amino acid residues are abbreviated as follows: alanine (Ala; A), asparagine (Asn; N), aspartic acid (Asp; D), arginine (Arg; R), cysteine (Cys; C), glutamic acid (Glu; E), glutamine (Gln; Q), glycine (Gly; G), histidine (His; H), isoleucine (Ile; I), leucine (Leu; L), lysine (Lys; K), methionine (Met; M), phenylalanine (Phe; F), proline (Pro; P), serine (Ser; S), threonine (Thr; T), tryptophan (Trp; W), tyrosine (Tyr; Y), and valine (Val; V).

Substitution and replacement rules. Generally speaking, amino acids with similar properties will have similar effects after replacement. For example, conservative amino acid replacements may occur in the above homologous proteins. "Conservative amino acid replacements" include but are not limited to:

hydrophobic amino acids (Ala, Cys, Gly, Pro, Met, Val, Ile, Leu) are replaced by other hydrophobic amino acids;

Substitution of hydrophobic amino acids with bulky side chains (Phe, Tyr, Trp) by other hydrophobic amino acids with bulky side chains;

Amino acids with positively charged side chains (Arg, His, Lys) are replaced by other amino acids with positively charged side chains;

Amino acids with polar, uncharged side chains (Ser, Thr, Asn, Gln) are replaced by other amino acids with polar, uncharged side chains.

A person skilled in the art may also perform conservative substitutions on amino acids according to amino acid substitution rules well known to those skilled in the art, such as the "blosum62 scoring matrix" in the prior art.

In this application, only the RNA ligase shown in SEQ ID NO: 1, or an enzyme with more than 70% identity with the RNA ligase shown in SEQ ID NO: 1, can be used to catalyze the formation of a phosphodiester bond between the phosphate group and the hydroxyl group of the substrate in this application to obtain the product Nedosiran. In the relevant experiments of this application, the inventors obtained the RNA ligase shown in SEQ ID NO: 1 that can synthesize Nedosiran by screening from a large number of enzymes. The negative results, which accounted for a large proportion of the experiments, showed that most RNA ligases were difficult to catalyze the synthesis of Nedosiran, including but not limited to the RNA ligases shown in SEQ ID NO: 2 to SEQ ID NO: 4. In this application specification, only SEQ ID NO: 2 to SEQ ID NO: 4 are used as examples to reflect this type of RNA ligase that has no catalytic activity in the synthesis of Nedosiran.

In a preferred embodiment, the sense chain substrate fragment and the antisense chain substrate fragment each include 2, the sense chain substrate fragment includes a first sense chain substrate fragment and a second sense chain substrate fragment, and the antisense chain substrate includes a first antisense chain substrate fragment and a second antisense chain substrate fragment; the preparation method includes: mixing the first sense chain substrate fragment, the second sense chain substrate fragment, the first antisense chain substrate fragment and the second antisense chain substrate fragment, using RNA ligase to catalyze the connection of the first sense chain substrate fragment and the second sense chain substrate fragment to form a sense chain, catalyzing the connection of the first antisense chain substrate fragment and the second antisense chain substrate fragment to form an antisense chain, and the sense chain and the antisense chain form Nedosiran through base complementary pairing.

In a preferred embodiment, the nucleotide sequence of the first sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 5, and the nucleotide sequence of the second sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 6; preferably, the nucleotide sequence of the first antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 8, and the nucleotide sequence of the second antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 7; preferably, the nucleotide sequence of the first sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 9, and the nucleotide sequence of the second sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 10; preferably, the nucleotide sequence of the first antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 12, and the nucleotide sequence of the second antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 11.

Nedosiran can be prepared using the above preparation method and the substrate fragments shown in SEQ ID NO: 5-SEQ ID NO: 8 or SEQ ID NO: 9-SEQ ID NO: 12. However, it should be noted that the selection of substrates is not limited to the substrate fragments shown in SEQ ID NO: 5-SEQ ID NO: 8 or SEQ ID NO: 9-SEQ ID NO: 12. All substrates that can be combined to form a sense chain and an antisense chain can be applied to the above preparation method. The above preparation method is suitable for the preparation of Nedosiran but is not limited to the difference in substrate connection positions. The above preparation has a good connection effect for the connection of the sense chain sequence and the antisense chain sequence of Nedosiran. The number of sense chain substrates or antisense chain substrates includes but is not limited to 2, 3, 4 or even more.

SEQ ID NO: 5: AmsUmGfUmUfGmUmCfCfUfUfUmUfUmAf.

SEQ ID NO: 6: UmCfUmGmAmGmCmAmGmCmCmGm*Am*Am*Am*GmGmCmUmGmCm.

SEQ ID NO: 7: GmAfCmAfAmCfAmUmsGmsGm.

SEQ ID NO: 8: U*sCfsAfsGmAfUmAfAmAfAfAmGm.

SEQ ID NO: 9: AmsUmGUmUfGmUmCfCf.

SEQ ID NO: 10: UfUfUmUfUmAfUmCfUmGmAmGmCmAmGmCmCmGm*Am*Am*Am*GmGmCmUmGmCm.

SEQ ID NO: 11: CmAfAmCfAmUmsGmsGm.

SEQ ID NO: 12: U*sCfsAfsGmAfUmAfAmAfAfAmGmGmAf.

In a preferred embodiment, the 3' end of the first sense chain substrate fragment and the 5' end of the second sense chain substrate fragment are connected under the catalysis of RNA ligase to form a sense chain; the 3' end of the first antisense chain substrate fragment and the 5' end of the second antisense chain substrate fragment are connected under the catalysis of RNA ligase to form an antisense chain; preferably, in the above preparation method, the 5' end of the first sense chain substrate fragment is a hydroxyl group, and the 3' end is a hydroxyl group; the 5' end of the second sense chain substrate fragment is a phosphate group, and the 3' end is an R group; the 5' end of the first antisense chain substrate fragment is a hydroxyl group, and the 3' end is a hydroxyl group; the 5' end of the second antisense chain substrate fragment is a phosphate group, and the 3' end is a hydroxyl group.

In a preferred embodiment, the sense chain substrate fragment and the antisense chain substrate fragment each include 3, the sense chain substrate fragment includes a first sense chain substrate fragment, a second sense chain substrate fragment and a third sense chain substrate fragment; the antisense chain substrate fragment includes a first antisense chain substrate fragment, a second antisense chain substrate fragment and a third antisense chain substrate fragment; preferably, the preparation method includes: mixing the first sense chain substrate fragment, the second sense chain substrate fragment, the third sense chain substrate fragment, the first antisense chain substrate fragment, the second antisense chain substrate fragment and the third antisense chain substrate fragment, under the catalytic action of RNA ligase, connecting the first sense chain substrate fragment, the second sense chain substrate fragment and the third sense chain substrate fragment to form a sense chain, catalyzing the connection of the first antisense chain substrate fragment, the second antisense chain substrate fragment and the third antisense chain substrate fragment to form an antisense chain, and the sense chain and the antisense chain form Nedosiran through base complementary pairing; preferably, annealing the sense chain substrate fragment and the antisense chain substrate fragment and mixing them with RNA ligase to obtain Nedosiran.

In a preferred embodiment, the nucleotide sequence of the above-mentioned first sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 13; the nucleotide sequence of the second sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 14; the nucleotide sequence of the third sense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 15; preferably, the nucleotide sequence of the first antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 18; the nucleotide sequence of the second antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 17; the nucleotide sequence of the third antisense chain substrate fragment is the nucleotide sequence shown in SEQ ID NO: 16.

SEQ ID NO: 13: AmsUmGfUmUfGm.

SEQ ID NO: 14: UmCfCfUfUfUmUfUm.

SEQ ID NO: 15: AfUmCfUmGmAmGmCmAmGmCmCmGm*Am*Am*Am*GmGmCmUmGmCm.

SEQ ID NO: 16: CfAmUmsGmsGm.

SEQ ID NO: 17: AfAmGmGmAfCmAfAm.

SEQ ID NO: 18: U*sCfsAfsGmAfUmAfAmAf.

In a preferred embodiment, the concentrations of the sense strand substrate fragment and the antisense strand substrate fragment are independently selected from 0.1-4.5 mM; preferably, the reaction system formed by mixing the sense strand substrate fragment, the antisense strand substrate fragment and RNA ligase also includes ATP, Tris-HCl, MgCl ₂ and DTT; preferably, the reaction temperature of the preparation method is 10-40°C, more preferably 15-30°C; preferably, the reaction time of the preparation method is 2-48h, more preferably 12-24h.

The concentrations of the sense strand substrate fragment and the antisense strand substrate fragment are each selected from, including but not limited to, 0.1, 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0 or 4.5 mM; the reaction temperature of the preparation method includes but is not limited to 10, 15, 16, 20, 25, 30, 35 or 40°C; the reaction time of the preparation method includes but is not limited to 2, 5, 10, 15, 16, 20, 24, 25, 30, 35, 40, 45 or 48h.

The beneficial effects of the present application will be further explained in detail below in conjunction with specific embodiments.

Example 1

Substrate fragments 1 to 4 were added to a clean reagent bottle in an equimolar ratio and mixed to obtain a substrate mixture. The concentration of each substrate in the substrate mixture was 2.5 mM. The sequences of substrate fragments 1 to 4 are shown in Table 1, and the length unit is nt. After the substrate fragment mixture is annealed, an RNA fragment mixture is obtained. The reaction system was set to 10 μL, and the reaction system included 100 μM RNA fragment mixture, 50 mM Tris-HCl, 10 eq ATP, 100 eq MgCl ₂ , 10 eq DTT (1 eq = 100 μM), and RNA ligases Ligase 25, Ligase 11, Ligase 20 and Ligase 32 were added at a final concentration of 0.2 mg/mL. The reaction system was reacted at 16°C for 16 hours. The obtained reaction system was inactivated by 80°C for 5 minutes, and the precipitate was removed by centrifugation at 12000 rpm. The schematic diagram of the enzyme-catalyzed ligation reaction is shown in Figure 1.

The products catalyzed by RNA ligase Ligase 25, Ligase 11, Ligase 20 and Ligase 32 were subjected to SDS-PAGE detection. The electrophoresis results of the products catalyzed by RNA ligase Ligase25 and Ligase11 are shown in Figure 3. In Figure 3, lane M represents the RNA molecule standard (marker), lane 1 represents the reaction system of Ligase 25, and lane 2 represents the reaction system of Ligase11. The yield was estimated based on the grayscale analysis results of the target band in the Urea-PAGE results, and the final yield results are shown in Table 2.

Four single-stranded RNA fragments were prepared using a solid phase synthesis method.

Table 1

.

Among them, the single m after A, C, G or U indicates the 2'methoxy modification of the ribonucleotide, f indicates the modification of the 2'fluorine of the ribonucleotide, "m*" indicates the modification group of the 2'R side chain of the ribose in the ribonucleotide; s before A, C, G or U (such as "sUm", "sAf", etc.) indicates the thio modification of the 5'phosphate of the ribonucleotide. "Gm*" is used as an example to illustrate the connection of the 2'R group, as shown in the following structural formula.

.

The ribonucleotides at positions 1, 2, 4, 6, 7, 12 and 14 of substrate 1 have 2' methoxy modifications, the ribonucleotides at positions 3, 5, 8, 9, 10, 11, 13 and 15 have 2' fluorine modifications, and the 5' phosphate on the ribonucleotide at position 2 has a thio modification.

The ribonucleotides at positions 1, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 and 21 of substrate 2 have 2' methoxy modifications, the ribonucleotide at position 2 has 2' fluorine modification, and the ribonucleotides at positions 12, 13, 14 and 15 have 2' R-group side chain modifications.

Substrate 3 has 2' methoxy modification at ribonucleotides 1, 3, 5, 7, 8, 9 and 10, and 2' fluorine modification at ribonucleotides 2, 4 and 6. The 5' phosphates on ribonucleotides 9 and 10 have thio modification.

Substrate 4 has 2' methoxy modifications at ribonucleotides 4, 6, 8, 11 and 12, and 2' fluorine modifications at ribonucleotides 2, 3, 5, 7, 9 and 10. The 5' phosphates on ribonucleotides 2, 3 and 4 have thio modifications. Ribonucleotide 1 has a 2' R-side chain modification.

The positive sense chain of the prepared Nedosiran is AmsUmGfUmUfGmUmCfCfUfUfUmUfUmAfUmCfUmGmAmGmCmAmGmCmCmGm*Am*Am*Am*GmGmCmUmGmCm (SEQ ID NO: 19), and the antisense chain is U*sCfsAfGmsAfUmAfAmAfAfAmGmGmAfCmAfAmCfAmUmsGmsGm (SEQ ID NO: 20).

Table 2

.

In expressing the product yield, “++” indicates a yield of 25-50% (excluding the endpoint value of 50%), “+++” indicates a yield of 50-75%, and “++++” indicates a yield of >75%.

The grayscale data of the product and substrate are obtained by grayscale analysis of the Urea-PAGE gel electrophoresis result image. The yield calculation formula in this embodiment is: yield = product grayscale data/(product grayscale data + substrate grayscale data).

Example 2

Add the substrate fragments 1 to 4 in an equimolar ratio to a clean reagent bottle, mix well to obtain a substrate mixture, and the concentration of each substrate in the substrate mixture is 2.5mM. After the substrate mixture is annealed, a mixed solution of RNA fragments of substrates 1 to 4 is obtained. The reaction system is set to 50μL, and the reaction system includes 800μM RNA fragment mixture, 50mM Tris-HCl, 4eq ATP, 100eq MgCl ₂ , 10eq DTT (1eq=800μM), and the RNA ligase Ligase 25 with high catalytic activity in Example 1 is added at a final concentration of 0.2mg/mL. The reaction system is reacted at 16℃ for 16h. After the reaction is completed, heat at 80℃ for 5min to inactivate the protein, and centrifuge to remove the precipitate.

The product catalyzed by Ligase 25 was subjected to HPLC and LC-MS detection, as shown in FIG4 . The yield was calculated based on the statistical results of the target peak area in the HPLC results, and the results are shown in Table 3 .

Table 3

.

In expressing the product yield, “+++” means the yield is 90-95% (excluding the 95% endpoint value), and “++++” means the yield is >95%.

The molecular weight of the positive chain product identified by LC-MS was 11871.88, and the molecular weight of the antisense chain product was 7396.14. The theoretical values of the positive chain product were 11871.85±8, and the theoretical values of the antisense chain product were 7396.12±8, indicating that Nedosiran was generated by Ligase 25 ligation. The detection result is shown in Figure 5.

Example 3

Add substrates 1 to 4 in an equimolar ratio to a clean reagent bottle, mix well to obtain a substrate mixture, and the concentration of each substrate in the substrate mixture is 2.5 mM. After the substrate mixture is annealed, a mixture of RNA fragments of substrates 1 to 4 is obtained. The reaction system is set to 10 mL, and the reaction system includes 800 μM RNA fragment mixture, 50 mM Tris-HCl, 4 eq ATP, 12.5 eq MgCl ₂ , 1.25 eq DTT (1 eq = 800 μM), and RNA ligase Ligase 25 is added at a final concentration of 0.2 mg/mL. The reaction system is reacted at 16°C for 16 hours. The obtained reaction system was heated at 50°C for 10-20 min to inactivate the protein, and the precipitate was removed by centrifugation at 12000 rpm. The supernatant was purified using a Nano-Q column, and the obtained product was gradient eluted with NaCl and desalted by membrane packaging (molecular weight cutoff 1 kDa). The product was freeze-dried, and the yield was calculated to be 76.60% and the purity was 96.00%.

Example 4

Add substrates 5 to 8 in an equimolar ratio to a clean reagent bottle, mix well to obtain a substrate mixture, and the concentration of each substrate in the substrate mixture is 2.5 mM. The sequences of substrates 5 to 8 are shown in Table 4. After the substrate mixture is annealed, a mixture of RNA fragments of substrates 9 to 14 is obtained. The reaction system is set to 50 μL, and the reaction system includes 800 μM RNA fragment mixture, 50 mMTris-HCl, 4 eq ATP, 12.5 eq MgCl ₂ , 1.25 eq DTT (1 eq = 800 μM); add RNA ligase Ligase 25 at a final concentration of 0.2 mg/mL. The reaction system is reacted at 16°C for 16 hours. The obtained reaction system was inactivated by 80°C for 5 min to inactivate the ligase, and the precipitate was removed by centrifugation at 12000 rpm. The product catalyzed by Ligase 25 was detected by HPLC. The enzyme activity was measured by the rough estimated proportion of the product peak in the HPLC data of the reaction system sample. The results showed that the yield was "+++" and the target peak accounted for 90.1% of the sample.

Table 4

.

Among them, the single m after A, C, G or U indicates the 2' methoxy modification of the ribonucleotide, f indicates the 2' fluorine modification of the ribonucleotide, and s before A, C, G or U (such as "sUm", "sAf", etc.) indicates the thio modification of the 5' phosphate of the ribonucleotide. "m*" indicates the modification group of the 2' R side chain of the ribose in the ribonucleotide.

The ribonucleotides at positions 1, 2, 4, 6 and 7 of substrate 5 have 2' methoxy modifications, and the ribonucleotides at positions 3, 5, 8 and 9 have 2' fluorine modifications. The 5' phosphate on the ribonucleotide at position 2 has a thio modification.

The ribonucleotides at positions 2, 3, 5, 7, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26 and 27 of substrate 6 have 2' methoxy modifications, the ribonucleotides at positions 1, 4, 6 and 8 have 2' fluorine modifications, and the ribonucleotides at positions 18, 19, 20 and 21 have 2' R-group side chain modifications.

The ribonucleotides at positions 1, 3, 5, 6, 7 and 8 of substrate 7 have 2' methoxy modifications, and the ribonucleotides at positions 2 and 4 have 2' fluorine modifications. The 5' phosphates at positions 7 and 8 have thio modifications.

Substrate 8 has 2' methoxy modifications at ribonucleotides 4, 6, 8, 11, 12 and 13, and 2' fluorine modifications at ribonucleotides 2, 3, 5, 7, 9, 10 and 14. The 5' phosphates on ribonucleotides 2, 3 and 4 have thio modifications. Ribonucleotide 1 has a 2' R-side chain modification.

The positive sense chain of the prepared Nedosiran is AmsUmGfUmUfGmUmCfCfUfUfUmUfUmAfUmCfUmGmAmGmCmAmGmCmCmGm*Am*Am*Am*GmGmCmUmGmCm (SEQ ID NO: 19), and the antisense chain is U*sCfsAfsGmAfUmAfAmAfAfAmGmGmAfCmAfAmCfAmUmsGmsGm (SEQ ID NO: 20).

Example 5

Add substrates 9 to 14 in an equimolar ratio to a clean reagent bottle, mix well to obtain a substrate mixture, and the concentration of each substrate in the substrate mixture is 2.5 mM. The sequences of substrates 9 to 14 are shown in Table 5. After the substrate mixture is annealed, a mixture of RNA fragments of substrates 5 to 8 is obtained. The reaction system is set to 50 μL. The reaction system includes 800 μM RNA fragment mixture, 50 mM Tris-HCl, 4 eq ATP, 12.5 eq MgCl ₂ , 1.25 eq DTT (1 eq = 800 μM), and RNA ligase Ligase 25 is added at a final concentration of 0.2 mg/mL. The reaction system is reacted at 16°C for 16 hours. The obtained reaction system was inactivated by 80°C for 5 min to inactivate the ligase, and the precipitate was removed by centrifugation at 12000 rpm. The product catalyzed by Ligase 25 was detected by HPLC. The enzyme activity was measured by the rough estimated proportion of the product peak in the HPLC data of the reaction system sample. The results showed that the yield was "+++" and the target peak accounted for 93.5% in the sample.

Table 5

.

Among them, the single m after A, C, G or U indicates the 2' methoxy modification of the ribonucleotide, f indicates the 2' fluorine modification of the ribonucleotide, and s before A, C, G or U (such as "sUm", "sAf", etc.) indicates the thio modification of the 5' phosphate of the ribonucleotide. "m*" indicates the modification group of the 2' R side chain of the ribose in the ribonucleotide.

The ribonucleotides at positions 1, 2, 4 and 6 of substrate 9 have 2' methoxy modifications, the ribonucleotides at positions 3 and 5 have 2' fluorine modifications, and the 5' phosphate on the ribonucleotide at position 2 has a thio modification.

The ribonucleotides at positions 1, 6 and 8 of substrate 10 have 2' methoxy modifications, and the ribonucleotides at positions 2, 3, 4, 5 and 7 have 2' fluorine modifications.

The ribonucleotides at positions 2, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 and 22 of substrate 11 have 2' methoxy modifications, the ribonucleotides at positions 1 and 3 have 2' fluorine modifications, and the ribonucleotides at positions 13, 14, 15 and 16 have 2' R-group side chain modifications.

The ribonucleotides at positions 2, 3, 4 and 5 of substrate 12 have 2' methoxy modifications, and the ribonucleotide at position 1 has 2' fluorine modification. The 5' phosphates on the ribonucleotides at positions 4 and 5 have thio modification.

The ribonucleotides at positions 2, 3, 4, 6 and 8 of substrate 13 have 2' methoxy modifications, and the ribonucleotides at positions 1, 5 and 7 have 2' fluorine modifications.

The ribonucleotides at positions 4, 6 and 8 of substrate 14 have 2' methoxy modifications, the ribonucleotides at positions 2, 3, 5, 7 and 9 have 2' fluorine modifications, the 5' phosphates on the ribonucleotides at positions 2, 3 and 4 have thio modifications, and the ribonucleotide at position 1 has a 2' R group side chain modification.

The positive sense chain of the prepared Nedosiran is AmsUmGfUm UfGmUmCf CfUfUfUm UfUmAfUmCfUmGmAm GmCmAmGmCmCmGm*Am*Am*Am*GmGm CmUmGmCm (SEQ ID NO: 19), and the antisense chain is U*sCfsAfsGmAfUmAfAmAfAfAmGmGmAfCmAfAmCfAmUmsGmsGm (SEQ ID NO: 20).

Example 6

The average yield of full-length Nedosiran product synthesized using solid phase synthesis was 39.1%, and the total proportion of N+1 and N-1 impurities was 1.52%.

The yield of the Nedosiran product prepared by the enzyme-linked method of the present invention is 84.05%, the yield using the solid phase synthesis substrate is 32.9%, and the yield of the overall process after multiplication is 31.6%. Although the yield of the overall process is slightly lower than the average yield of the product obtained by the solid phase synthesis method, the total proportion of N+1 and N-1 impurities is only 0.4%, which is much lower than the proportion of such impurities in the process of synthesizing Nedosiran by solid phase synthesis.

From the above description, it can be seen that the above embodiments of the present invention achieve the following technical effects: in the preparation method of the present application, single-stranded RNA fragments designed based on the sequence of Nedosiran are catalyzed by RNA ligase to form Nedosiran, thereby realizing the preparation of such siRNA drugs by biosynthesis. Compared with the chemical synthesis preparation method, the product obtained by the preparation method of the present application has high purity, less impurities, simple preparation process, mild reaction conditions, low amount of organic reagents, reduced production costs, and is easy to achieve scale-up industrial production.

The above description is only a preferred embodiment of the present invention and is not intended to limit the present invention. For those skilled in the art, the present invention may have various modifications and variations. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present invention shall be included in the protection scope of the present invention.

Claims (13)

1. A method of preparing Nedosiran, wherein Nedosiran is a double-stranded siRNA consisting of complementarily paired sense and antisense strands;

The preparation method comprises the following steps:

Mixing a sense strand substrate fragment, an antisense strand substrate fragment, and an RNA ligase, wherein the sense strand substrate fragment is capable of constituting the sense strand and the antisense strand substrate fragment is capable of constituting the antisense strand;

The sense strand substrate fragment and the antisense strand substrate fragment are connected through hydrogen bonds formed by base complementation, and the head base and the tail base of the sense strand substrate fragment and the antisense strand substrate fragment are not connected with each other to form a double-stranded nucleotide structure containing a nick;

connecting bases at two ends of the nick with a phosphodiester bond by using the RNA ligase to form Nedosiran;

the bases at the two ends of the notch are respectively the 5 'end and the 3' end of different substrate fragments, the 5 'end is phosphate radical, and the 3' end is hydroxyl radical;

connecting the phosphate at the 5 'end and the hydroxyl at the 3' end at the upstream and downstream of the nick by using the RNA ligase to form the phosphodiester bond, thereby obtaining Nedosiran;

The RNA ligase is a polypeptide having the sequence of SEQ ID NO:1, and a RNA ligase having the amino acid sequence shown in seq id no;

Or with SEQ ID NO:1, and has an activity of catalyzing the formation of phosphodiester bonds.

2. The method of claim 1, wherein the sense strand has a nucleotide sequence of SEQ ID NO:19, and the nucleotide sequence of the antisense strand is the nucleotide sequence shown in SEQ ID NO:20, and a nucleotide sequence shown in seq id no.

3. The method of any one of claims 1-2, wherein the sense strand substrate fragment comprises 2 or more and the antisense strand substrate fragment comprises 2 or more;

The length of the sense strand substrate fragment is 2-34nt;

The length of the antisense strand substrate fragment is 2-20nt.

4. The method of making according to claim 1, wherein the sense strand substrate fragment and the antisense strand substrate fragment each comprise 2, the sense strand substrate fragment comprises a first sense strand substrate fragment and a second sense strand substrate fragment, and the antisense strand substrate fragment comprises a first antisense strand substrate fragment and a second antisense strand substrate fragment;

The preparation method comprises the following steps: mixing the first sense strand substrate fragment, the second sense strand substrate fragment, the first antisense strand substrate fragment and the second antisense strand substrate fragment, and under the catalysis of the RNA ligase, the first sense strand substrate fragment and the second sense strand substrate fragment are connected to form the sense strand, catalyzing the first antisense strand substrate fragment and the second antisense strand substrate fragment to be connected to form the antisense strand, and the sense strand and the antisense strand are formed into the Nedosiran by base complementary pairing.

5. The method of claim 4, wherein the nucleotide sequence of the first sense strand substrate fragment is SEQ ID NO:5, and the nucleotide sequence of the second sense strand substrate fragment is SEQ ID NO:6, a nucleotide sequence shown in seq id no;

the nucleotide sequence of the first antisense strand substrate fragment is SEQ ID NO:8, and the nucleotide sequence of the second antisense strand substrate fragment is SEQ ID NO:7, and a nucleotide sequence shown in the sequence No.

6. The method of claim 4, wherein the first sense strand substrate fragment has the nucleotide sequence of SEQ ID NO:9, and the nucleotide sequence of the second sense strand substrate fragment is set forth in SEQ ID NO:10, a nucleotide sequence shown in the sequence of seq id no;

The nucleotide sequence of the first antisense strand substrate fragment is SEQ ID NO:12, and the nucleotide sequence of the second antisense strand substrate fragment is set forth in SEQ ID NO:11, and a nucleotide sequence shown in seq id no.

7. The method of claim 4, wherein the 3 'end of the first sense strand substrate fragment is ligated to the 5' end of the second sense strand substrate fragment under the catalysis of the RNA ligase to form the sense strand; the 3 'end of the first antisense strand substrate fragment is ligated to the 5' end of the second antisense strand substrate fragment under the catalysis of the RNA ligase to form the antisense strand.

8. The method of claim 4, wherein the first sense strand substrate fragment has a hydroxyl group at the 5 'end and a hydroxyl group at the 3' end; the 5 'end of the second sense strand substrate fragment is a phosphate group, and the 3' end is an R group;

the 5 'end of the first antisense strand substrate fragment is a hydroxyl group, and the 3' end of the first antisense strand substrate fragment is a hydroxyl group; the 5 'end of the second antisense strand substrate fragment is a phosphate group, and the 3' end is a hydroxyl group.

9. The method of claim 1, wherein the sense strand substrate fragment and the antisense strand substrate fragment each comprise 3,

The sense strand substrate fragments comprise a first sense strand substrate fragment, a second sense strand substrate fragment, and a third sense strand substrate fragment;

The antisense strand substrate fragments include a first antisense strand substrate fragment, a second antisense strand substrate fragment, and a third antisense strand substrate fragment.

10. The preparation method according to claim 9, characterized in that the preparation method comprises: mixing the first sense strand substrate fragment, the second sense strand substrate fragment, the third sense strand substrate fragment, the first antisense strand substrate fragment, the second antisense strand substrate fragment, and the third antisense strand substrate fragment, and under the catalytic action of the RNA ligase, the first sense strand substrate fragment, the second sense strand substrate fragment, and the third sense strand substrate fragment are joined to form the sense strand, and the first antisense strand substrate fragment, the second antisense strand substrate fragment, and the third antisense strand substrate fragment are joined to form the antisense strand, and the sense strand and the antisense strand are paired by base complementarity to form the Nedosiran.

11. The method of claim 9, wherein the first sense strand substrate fragment is SEQ ID NO:13, a nucleotide sequence shown in seq id no;

the nucleotide sequence of the second sense strand substrate fragment is SEQ ID NO:14, a nucleotide sequence shown in seq id no;

The nucleotide sequence of the third sense strand substrate fragment is SEQ ID NO:15, a nucleotide sequence shown in seq id no;

the nucleotide sequence of the first antisense strand substrate fragment is SEQ ID NO:18, a nucleotide sequence shown in seq id no;

the nucleotide sequence of the second antisense strand substrate fragment is SEQ ID NO:17, a nucleotide sequence shown in seq id no;

The nucleotide sequence of the third antisense strand substrate fragment is SEQ ID NO:16, and a nucleotide sequence shown in seq id no.

12. The method of claim 1, wherein the sense strand substrate fragment and the antisense strand substrate fragment concentrations are each independently selected from 0.1-4.5mM;

The reaction system formed by mixing the sense strand substrate fragment, the antisense strand substrate fragment and the RNA ligase further comprises ATP, tris-HCl, mgCl ₂ and DTT.

13. The preparation method according to claim 1, wherein the reaction temperature of the preparation method is 10-40 ℃;

the reaction time of the preparation method is 2-48h.