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Literature DB >> 20157912

Chemical protein synthesis by kinetically controlled ligation of peptide O-esters.

Ji-Shen Zheng¹, Hong-Kui Cui, Ge-Min Fang, Wei-Xian Xi, Lei Liu.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2010 PMID： 20157912 DOI： 10.1002/cbic.200900789

Source DB: PubMed Journal: Chembiochem ISSN： 1439-4227 Impact factor: 3.164

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8 in total

1. Chemical synthesis of proteins using peptide hydrazides as thioester surrogates.

Authors: Ji-Shen Zheng; Shan Tang; Yun-Kun Qi; Zhi-Peng Wang; Lei Liu
Journal: Nat Protoc Date: 2013-11-14 Impact factor: 13.491

2. One-pot chemical synthesis of small ubiquitin-like modifier protein-peptide conjugates using bis(2-sulfanylethyl)amido peptide latent thioester surrogates.

Authors: Emmanuelle Boll; Hervé Drobecq; Nathalie Ollivier; Annick Blanpain; Laurent Raibaut; Rémi Desmet; Jérôme Vicogne; Oleg Melnyk
Journal: Nat Protoc Date: 2015-01-15 Impact factor: 13.491

3. Development of a Chemical Methodology for the Preparation of Peptide Thioesters Applicable to Naturally Occurring Peptides Using a Sequential Quadruple Acyl Transfer System.

Authors: Yusuke Tsuda; Akira Shigenaga; Kohei Tsuji; Masaya Denda; Kohei Sato; Keisuke Kitakaze; Takahiro Nakamura; Tsubasa Inokuma; Kohji Itoh; Akira Otaka
Journal: ChemistryOpen Date: 2015-04-28 Impact factor: 2.911

Chemical protein synthesis by kinetically controlled ligation of peptide O-esters.

1. Chemical synthesis of proteins using peptide hydrazides as thioester surrogates.

2. One-pot chemical synthesis of small ubiquitin-like modifier protein-peptide conjugates using bis(2-sulfanylethyl)amido peptide latent thioester surrogates.

3. Development of a Chemical Methodology for the Preparation of Peptide Thioesters Applicable to Naturally Occurring Peptides Using a Sequential Quadruple Acyl Transfer System.

4. Accelerating chemoselective peptide bond formation using bis(2-selenylethyl)amido peptide selenoester surrogates.

5. Traceless β-mercaptan-assisted activation of valinyl benzimidazolinones in peptide ligations.

6. A new method of N to C sequential ligation using thioacid capture ligation and native chemical ligation.

7. Native Chemical Ligation of Highly Hydrophobic Peptides in Ionic Liquid-Containing Media.

8. Redox-Controlled Chemical Protein Synthesis: Sundry Shades of Latency.