Chemical Protein Synthesis Using a Second-Generation N-Acylurea Linker for the Preparation of Peptide-Thioester Precursors.
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Advances in Fmoc solid-phase peptide synthesisEfficient enzymatic cyclization of an inhibitory cystine knot-containing peptideExpanding the chemical toolbox for the synthesis of large and uniquely modified proteins.Hybrid phase ligation for efficient synthesis of histone proteins.Chemical Synthesis of Phosphorylated Histone H2A at Tyr57 Reveals Insight into the Inhibition Mode of the SAGA Deubiquitinating Module.Accessing human selenoproteins through chemical protein synthesis.Modern tools for the chemical ligation and synthesis of modified peptides and proteins.Combination of Thiol-Additive-Free Native Chemical Ligation/Desulfurization and Intentional Replacement of Alanine with Cysteine.Serine promoted synthesis of peptide thioester-precursor on solid support for native chemical ligation.HF-Free Boc Synthesis of Peptide Thioesters for Ligation and CyclizationA Facile N-Mercaptoethoxyglycinamide (MEGA) Linker Approach to Peptide Thioesterification and Cyclization.Sequence Diversification by Divergent C-Terminal Elongation of Peptides.Exploiting the MeDbz Linker To Generate Protected or Unprotected C-Terminally Modified Peptides.Efficient synthesis of cysteine-rich cyclic peptides through intramolecular native chemical ligation of N-Hnb-Cys peptide crypto-thioesters.Palladium-Assisted Cleavage of Peptides and Proteins Containing a Backbone with Thiazolidine Linkage.Efficient synthesis of longer Aβ peptides via removable backbone modification.Synthesis of l- and d-Ubiquitin by One-Pot Ligation and Metal-Free Desulfurization.Design of Bivalent Nucleic Acid Ligands for Recognition of RNA-Repeated Expansion Associated with Huntington's Disease.Total chemical synthesis of ester-linked ubiquitinated proteins unravels their behavior with deubiquitinases.Expedient on-resin modification of a peptide C-terminus through a benzotriazole linker.An efficient solid-phase synthesis of peptidyl-N-acetylguanidines for use in native chemical ligation.Efficient Palladium-Assisted One-Pot Deprotection of (Acetamidomethyl)Cysteine Following Native Chemical Ligation and/or Desulfurization To Expedite Chemical Protein Synthesis.Epimerization-free access to C-terminal cysteine peptide acids, carboxamides, secondary amides, and esters via complimentary strategies.A straightforward method for automated Fmoc-based synthesis of bio-inspired peptide crypto-thioesters.Leveraging the Knorr Pyrazole Synthesis for the Facile Generation of Thioester Surrogates for use in Native Chemical LigationHF-Free Boc Synthesis of Peptide Thioesters for Ligation and Cyclization
P2860
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P2860
Chemical Protein Synthesis Using a Second-Generation N-Acylurea Linker for the Preparation of Peptide-Thioester Precursors.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Chemical Protein Synthesis Usi ...... Peptide-Thioester Precursors.
@en
type
label
Chemical Protein Synthesis Usi ...... Peptide-Thioester Precursors.
@en
prefLabel
Chemical Protein Synthesis Usi ...... Peptide-Thioester Precursors.
@en
P2093
P356
P1476
Chemical Protein Synthesis Usi ...... f Peptide-Thioester Precursors
@en
P2093
Brunello Nardone
Juan B Blanco-Canosa
Philip E Dawson
P304
P356
10.1021/JACS.5B03504
P407
P577
2015-06-02T00:00:00Z