Synthetic glycopeptides and glycoproteins as tools for biology.
about
Glycotherapy: new advances inspire a reemergence of glycans in medicinePeptide-Like Molecules (PLMs): A Journey from Peptide Bond Isosteres to Gramicidin S Mimetics and Mitochondrial Targeting Agents.Effect of distal sugar and interglycosidic linkage of disaccharides on the activity of proline rich antimicrobial glycopeptides.Ketone hydrosilylation with sugar silanes followed by intramolecular aglycone delivery: an orthogonal glycosylation strategy.Influence of solvent and intramolecular hydrogen bonding on the conformational properties of o-linked glycopeptidesGenome-scale metabolic reconstruction and in silico analysis of methylotrophic yeast Pichia pastoris for strain improvementA program for ligation at threonine sites: application to the controlled total synthesis of glycopeptides.Divergent behavior of glycosylated threonine and serine derivatives in solid phase peptide synthesis.Scalable synthesis of Fmoc-protected GalNAc-threonine amino acid and T(N) antigen via nickel catalysis.Toward Homogeneous Erythropoietin: Application of Metal Free Dethiylation in the Chemical Synthesis of the Ala79-Arg166 Glycopeptide Domain.Chemoenzymatic synthesis of glycopeptides and glycoproteins through endoglycosidase-catalyzed transglycosylation.Hierarchical assembly of model cell surfaces: synthesis of mucin mimetic polymers and their display on supported bilayers.Glycosynthases enable a highly efficient chemoenzymatic synthesis of N-glycoproteins carrying intact natural N-glycansExpeditious chemoenzymatic synthesis of homogeneous N-glycoproteins carrying defined oligosaccharide ligands.Chemical and chemoenzymatic synthesis of glycoproteins for deciphering functions.The Tn antigen-structural simplicity and biological complexity.Recent applications of thiol-ene coupling as a click process for glycoconjugation.Microwave heating in solid-phase peptide synthesis.Toward automated oligosaccharide synthesis.Stereoselective glycosylation of glucosamine: the role of the N-protecting group.Modulating glycosylation with exogenous nucleophiles: an overview.Emerging bioinspired polymers: glycopolypeptides.Native chemical ligation: a boon to peptide chemistry.Targeted methods for quantitative analysis of protein glycosylation.OGlcNAcylation and phosphorylation have similar structural effects in α-helices: post-translational modifications as inducible start and stop signals in α-helices, with greater structural effects on threonine modification.Synthesis, biological evaluation and structural characterization of novel glycopeptide analogues of nociceptin N/OFQ.Chemoselective synthesis of diaryl disulfides via a visible light-mediated coupling of arenediazonium tetrafluoroborates and CS2.Synthesis of glycosylated β³-homo-threonine conjugates for mucin-like glycopeptide antigen analogues.Facile preparation of fluorescent neoglycoproteins using p-nitrophenyl anthranilate as a heterobifunctional linker.Targeted antigen delivery by an anti-class II MHC VHH elicits focused αMUC1(Tn) immunity.Development of a universal glycosyltransferase assay amenable to high-throughput formats.Sugar-assisted ligation in glycoprotein synthesis.Dechalcogenative allylic selenosulfide and disulfide rearrangements: complementary methods for the formation of allylic sulfides in the absence of electrophiles. Scope, limitations, and application to the functionalization of unprotected peptides inSugar-assisted glycopeptide ligation with complex oligosaccharides: scope and limitations.An efficient method for selectively imaging and quantifying in situ the expression of sialylated glycoproteins on living cells.Multi-component synthesis of peptide-sugar conjugates.Advances in glycoprotein synthesis.Comparing naturally occurring glycosylated forms of proline rich antibacterial peptide, Drosocin.Obstacles and solutions for chemical synthesis of syndecan-3 (53-62) glycopeptides with two heparan sulfate chains.Systematic dissection of an aminopyrrolic cage receptor for β-glucopyranosides reveals the essentials for effective recognition.
P2860
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P2860
Synthetic glycopeptides and glycoproteins as tools for biology.
description
2004 nî lūn-bûn
@nan
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Synthetic glycopeptides and glycoproteins as tools for biology.
@ast
Synthetic glycopeptides and glycoproteins as tools for biology.
@en
type
label
Synthetic glycopeptides and glycoproteins as tools for biology.
@ast
Synthetic glycopeptides and glycoproteins as tools for biology.
@en
prefLabel
Synthetic glycopeptides and glycoproteins as tools for biology.
@ast
Synthetic glycopeptides and glycoproteins as tools for biology.
@en
P356
P1476
Synthetic glycopeptides and glycoproteins as tools for biology.
@en
P2093
Carolyn R Bertozzi
Matthew R Pratt
P356
10.1039/B400593G
P577
2004-12-13T00:00:00Z