Synthesis of thioester peptides for the incorporation of thioamides into proteins by native chemical ligation

被引:13
|
作者
Batjargal, Solongo [1 ]
Huang, Yun [1 ]
Wang, Yanxin J. [1 ]
Petersson, E. James [1 ]
机构
[1] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Thioamide; Native Chemical Ligation; Thioester; Fmoc SPPS; ALPHA-SYNUCLEIN; FMOC-SPPS; BACKBONE; DYNAMICS; STRATEGY; PROBES;
D O I
10.1002/psc.2589
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thioamides can be used as photoswitches, as reporters of local environment, as inhibitors of enzymes, and as fluorescence quenchers. We have recently demonstrated the incorporation of thioamides into polypeptides and proteins using native chemical ligation (NCL). In this protocol, we describe procedures for the synthesis of a thioamide precursor and an NCL-ready thioamide-containing peptide using Dawson's N-acyl-benzimidazolinone (Nbz) process. We include a description of the synthesis by NCL of a thioamide-labeled fragment of the neuronal protein -synuclein. Copyright (c) 2014 European Peptide Society and John Wiley & Sons, Ltd.
引用
收藏
页码:87 / 91
页数:5
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