Doelman et al., 2022 - Google Patents
Synthesis of glycopeptides and glycopeptide conjugatesDoelman et al., 2022
View HTML- Document ID
- 16776686657852967338
- Author
- Doelman W
- van Kasteren S
- Publication year
- Publication venue
- Organic & Biomolecular Chemistry
External Links
Snippet
Protein glycosylation is a key post-translational modification important to many facets of biology. Glycosylation can have critical effects on protein conformation, uptake and intracellular routing. In immunology, glycosylation of antigens has been shown to play a role …
- 238000003786 synthesis reaction 0 title abstract description 72
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/107—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
- C07K1/1072—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups
- C07K1/1077—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups by covalent attachment of residues other than amino acids or peptide residues, e.g. sugars, polyols, fatty acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4727—Mucins, e.g. human intestinal mucin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K9/00—Peptides having up to 20 amino acids, containing saccharide radicals and having a fully defined sequence; Derivatives thereof
- C07K9/001—Peptides having up to 20 amino acids, containing saccharide radicals and having a fully defined sequence; Derivatives thereof the peptide sequence having less than 12 amino acids and not being part of a ring structure
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/12—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by hydrolysis, i.e. solvolysis in general
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/06—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
- C07K1/061—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
- C12P21/005—Glycopeptides, glycoproteins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Doelman et al. | Synthesis of glycopeptides and glycopeptide conjugates | |
| Unverzagt et al. | Chemical assembly of N-glycoproteins: a refined toolbox to address a ubiquitous posttranslational modification | |
| Buskas et al. | Glycopeptides as versatile tools for glycobiology | |
| Seitz | Glycopeptide synthesis and the effects of glycosylation on protein structure and activity | |
| Herzner et al. | Synthesis of glycopeptides containing carbohydrate and peptide recognition motifs | |
| Grogan et al. | Homogeneous glycopeptides and glycoproteins for biological investigation | |
| Marcaurelle et al. | Chemoselective elaboration of O-linked glycopeptide mimetics by alkylation of 3-ThioGalNAc | |
| Davis | Synthesis of glycoproteins | |
| US7193034B2 (en) | Synthetic peptides, conjugation reagents and methods | |
| Fernández-Tejada et al. | Total synthesis of glycosylated proteins | |
| DK1520858T3 (en) | Process for Preparation of Glycopeptides with Asparagine-Linked Oligosaccharides | |
| Galibert et al. | Combining triazole ligation and enzymatic glycosylation on solid phase simplifies the synthesis of very long glycoprotein analogues | |
| Hojo et al. | Recent progress in the field of glycopeptide synthesis | |
| Dziadek et al. | Synthesis of tumor‐associated glycopeptide antigens for the development of tumor‐selective vaccines | |
| Wu et al. | Synthesis and immunological evaluation of the unnatural β-linked mucin-1 Thomsen–Friedenreich conjugate | |
| Wilkinson et al. | Synthesis of MUC1–lipopeptide chimeras | |
| Bello et al. | A quantitative and site-specific chemoenzymatic glycosylation approach for PEGylated MUC1 peptides | |
| Zhuang et al. | Recent advances in glycopeptide and glycoprotein synthesis: a refined synthetic probe towards the biological world | |
| Singh et al. | Positional scanning MUC1 glycopeptide library reveals the importance of PDTR epitope glycosylation for lectin binding | |
| Liu et al. | Advances in glycoprotein synthesis | |
| Dziadek et al. | Synthetic glycopeptides for the development of antitumour vaccines | |
| Ochiai et al. | Chemical and Chemoenzymatic Synthesis of Peptide and Protein Therapeutics Conjugated with Human N‐Glycans | |
| Pergolizzi et al. | Contemporary glycoconjugation chemistry | |
| Cudic et al. | Preparation of glycosylated amino acids suitable for Fmoc solid-phase assembly | |
| Masania et al. | Access to phosphoproteins and glycoproteins through semi-synthesis, Native Chemical Ligation and N→ S acyl transfer |