Towards the total chemical synthesis of integral membrane proteins:: a general method for the synthesis of hydrophobic peptide-αthioester building blocks

被引:79
作者
Johnson, Erik C. B.
Kent, Stephen B. H.
机构
[1] Inst Biophys Dynam, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Biochem, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
关键词
chemical protein synthesis; integral membrane proteins; diacylglycerol kinase; native chemical ligation; thioester;
D O I
10.1016/j.tetlet.2007.01.030
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Modification of a peptide-(alpha)thioester with a sequence of six arginines on the thioester leaving group can render soluble all peptides derived from a polytopic integral membrane protein. This strategy greatly simplifies the synthesis of peptide-(alpha)thioester building blocks for the total chemical synthesis of integral membrane proteins by native chemical ligation. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1795 / 1799
页数:5
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