Fmoc chemistry compatible thio-ligation assembly of proteins

被引:24
作者
Biancalana, S
Hudson, D
Songster, MF
Thompson, SA
机构
[1] Biosearch Technol Inc, Novato, CA 94949 USA
[2] Berlex Biosci, Richmond, CA 94804 USA
来源
LETTERS IN PEPTIDE SCIENCE | 2000年 / 7卷 / 05期
关键词
chemoselective ligation; Fmoc-methodology; iso-thiouronium salts; Kenner safety catch resin; native chemical ligation; peptide thioesters; peptide isomerisation; safety-catch linkers; solid-phase synthesis; thioester exchange;
D O I
10.1023/A:1011849912229
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
We describe, and compare, two methods which enable the assembly of proteins from peptide thioester fragments prepared by Fmoc chemistry mediated solid phase synthesis. The first, which utilizes iso-thiouronium salts, allows formation of thiophenyl esters directly from partially protected peptides, either in solution or on resin. The second uses `sulfonamide' based safety-catch resins. Data on yields, generality and potential for side-reactions are provided.
引用
收藏
页码:291 / 297
页数:7
相关论文
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[11]  
TAM JP, 1999, INNOVATION PERSPECTI, P1