Synthesis of multi-domain proteins using expressed protein ligation: Strategies for segmental isotopic labeling of internal regions

被引:23
作者
Blaschke, UK [1 ]
Cotton, GJ [1 ]
Muir, TW [1 ]
机构
[1] Rockefeller Univ, Lab Synthet Prot Chem, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
semi-synthesis technique; expressed protein ligation; isotopic labeling;
D O I
10.1016/S0040-4020(00)00830-9
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Here we describe how a sequential version of the protein semi-synthesis technique, Expressed Protein Ligation (EPL), can be used to assemble multiple (i.e. 3 or more) recombinantly-derived polypeptides segments into a target protein. Sequential EPL was successfully used to assembly the 304 amino acid eukaryotic adaptor protein, Crk-II, from three recombinant polypeptide segments in good yield. Moreover, the resulting multi-component ligation product was found to possess the expected biological activity in a series of ligand binding studies. By allowing the controlled assembly of 3 or more recombinant polypeptide segments, sequential EPL opens the door to the segmental isotopic labeling of internal regions of large proteins with NMR probe-nuclei. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:9461 / 9470
页数:10
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