Development of efficient methods for accomplishing cysteine-free peptide and glycopeptide coupling

被引:65
作者
Chen, Gong [1 ]
Wan, Qian [1 ]
Tan, Zhongping [1 ]
Kan, Cindy [1 ]
Hua, Zihao [1 ]
Ranganathan, Krishnakumar [1 ]
Danishefsky, Samuel J. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Bioorgan Chem Lab, New York, NY 10021 USA
关键词
coupling reactions; glycopeptides; glycoproteins; peptides; synthetic methods;
D O I
10.1002/anie.200702865
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As simple as A, B, C: Non-cysteine-based reiterative fragment coupling of glycopeptides involves a metal-free (TCEP) coupling of a peptidyl C-terminal phenolic ester containing an ortho-disulfide moiety (A) with an N-terminal glycopeptide whose C terminus is an alkyl thioester (B) to produce AB, whose N terminus contains an alkyl thioester. A AgCl-mediated coupling of AB with peptide C then produces the tridomainal peptide ABC. TCEP = tris (2-carboxyethyl)phosphine. (Chemical Equation Presented) © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:7383 / 7387
页数:5
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