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.
论文数: 0引用数: 0
h-index: 0
机构:Inst Biophys Dynam, Chicago, IL 60637 USA
Johnson, Erik C. B.
Kent, Stephen B. H.
论文数: 0引用数: 0
h-index: 0
机构:Inst Biophys Dynam, Chicago, IL 60637 USA
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
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.