Chemical assembly of N-glycoproteins: a refined toolbox to address a ubiquitous posttranslational modification.
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Advances in Fmoc solid-phase peptide synthesis(Quasi-)racemic X-ray structures of glycosylated and non-glycosylated forms of the chemokine Ser-CCL1 prepared by total chemical synthesisTotal chemical synthesis, refolding, and crystallographic structure of fully active immunophilin calstabin 2 (FKBP12.6)Total synthesis of glycosylated proteinsSynthetic Nucleosomes Reveal that GlcNAcylation Modulates Direct Interaction with the FACT ComplexEvaluation of the effect of post-translational modification toward protein structure: Chemical synthesis of glycosyl crambins having either a high mannose-type or a complex-type oligosaccharide.Chemical Synthesis of Glycoproteins with the Specific Installation of Gradient-Enriched 15 N-Labeled Amino Acids for Getting Insights into Glycoprotein Behavior.Specificity of O-glycosylation in enhancing the stability and cellulose binding affinity of Family 1 carbohydrate-binding modulesChemical synthesis of syndecan-3 glycopeptides bearing two heparan sulfate glycan chains.Total synthesis of homogeneous variants of hirudin P6: a post-translationally modified anti-thrombotic leech-derived protein.Convergent chemoenzymatic synthesis of a library of glycosylated analogues of pramlintide: structure-activity relationships for amylin receptor agonism.Efficient Chemoenzymatic Synthesis of an N-glycan Isomer Library.Tailored Synthesis of 162-Residue S-Monoglycosylated GM2-Activator Protein (GM2AP) Analogues that Allows Facile Access to a Protein Library.Fully Synthetic Granulocyte Colony-Stimulating Factor Enabled by Isonitrile-Mediated Coupling of Large, Side-Chain-Unprotected PeptidesEndo-F3 Glycosynthase Mutants Enable Chemoenzymatic Synthesis of Core-fucosylated Triantennary Complex Type Glycopeptides and Glycoproteins.Chemical and chemoenzymatic synthesis of glycoproteins for deciphering functions.Synthetic Glycoforms Reveal Carbohydrate-Dependent Bioactivity of Human Saposin D.Recent Developments in Synthetic Carbohydrate-Based Diagnostics, Vaccines, and Therapeutics.Chemical synthesis of erythropoietin glycoforms for insights into the relationship between glycosylation pattern and bioactivitySynthetic multivalent V3 glycopeptides display enhanced recognition by glycan-dependent HIV-1 broadly neutralizing antibodies.Convergent versus sequential protein synthesis: the case of ubiquitinated and glycosylated H2B.Combination of Thiol-Additive-Free Native Chemical Ligation/Desulfurization and Intentional Replacement of Alanine with Cysteine.The ENGases: versatile biocatalysts for the production of homogeneous N-linked glycopeptides and glycoproteins.Cooperative role of calnexin and TigA in Aspergillus oryzae glycoprotein folding.The total chemical synthesis of the monoglycosylated GM2 ganglioside activator using a novel cysteine surrogate.Accelerating chemoselective peptide bond formation using bis(2-selenylethyl)amido peptide selenoester surrogates.Serine promoted synthesis of peptide thioester-precursor on solid support for native chemical ligation.Broad substrate tolerance of tubulin tyrosine ligase enables one-step site-specific enzymatic protein labeling.Efficient synthesis of polypeptide-α-thioester by the method combining polypeptide expression and chemical activation for the semi-synthesis of interferon-γ having oligosaccharides.Total chemical synthesis and biological activities of glycosylated and non-glycosylated forms of the chemokines CCL1 and Ser-CCL1.Occurrence of free sialyl oligosaccharides related to N-glycans (sialyl free N-glycans) in animal sera.Synthesis of Glc1Man9-Glycoprotein Probes by a Misfolding/Enzymatic Glucosylation/Misfolding Sequence.Site-Selective Chemoenzymatic Glycosylation of an HIV-1 Polypeptide Antigen with Two Distinct N-Glycans via an Orthogonal Protecting Group Strategy.Imidazole-Aided Native Chemical Ligation: Imidazole as a One-Pot Desulfurization-Amenable Non-Thiol-Type Alternative to 4-Mercaptophenylacetic Acid.Systematic Synthesis and Binding Study of HIV V3 Glycopeptides Reveal the Fine Epitopes of Several Broadly Neutralizing Antibodies.An enzymatic strategy to asymmetrically branched N-glycans.ECBS & ICBS 2015 Joint Meeting: Bringing Chemistry to Life.Obstacles and solutions for chemical synthesis of syndecan-3 (53-62) glycopeptides with two heparan sulfate chains.Synthetic Three-Component HIV-1 V3 Glycopeptide Immunogens Induce Glycan-Dependent Antibody Responses.Highly Efficient Synthesis of Multiantennary Bisected N-glycans Based on Imidates.
P2860
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P2860
Chemical assembly of N-glycoproteins: a refined toolbox to address a ubiquitous posttranslational modification.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Chemical assembly of N-glycopr ...... osttranslational modification.
@en
type
label
Chemical assembly of N-glycopr ...... osttranslational modification.
@en
prefLabel
Chemical assembly of N-glycopr ...... osttranslational modification.
@en
P2860
P356
P1476
Chemical assembly of N-glycopr ...... osttranslational modification.
@en
P2093
Yasuhiro Kajihara
P2860
P304
P356
10.1039/C3CS35485G
P577
2013-02-13T00:00:00Z