Synthesis of palmitoylated Ras-peptides and -proteins

被引:15
作者
Brunsveld, L.
Kuhlmann, J.
Waldmann, H.
机构
[1] Max Planck Inst Mol Physiol, D-44227 Dortmund, Germany
[2] Chem Genom Ctr, D-44227 Dortmund, Germany
[3] Univ Dortmund, Fachbereich Chem, D-44221 Dortmund, Germany
关键词
bioorganic chemistry; lipoproteins; peptides; protein ligation; lipopeptides; GTPases;
D O I
10.1016/j.ymeth.2006.04.014
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this review, an overview is given and details are provided for the synthesis of lipidated Ras (rat-adeno-sarcoma)-peptides and -proteins. The progress made in the synthesis of the lipidated peptides from the Ras superfamily is discussed with special emphasis on the recently developed solid-phase synthesis methods, since these methods have turned out to be the preferred synthesis method for the majority of the required peptides. Solid-phase lipopeptide synthesis has given access to native and modified peptides on a scale that allows peptide-consuming studies like for ligation to proteins and concomitant X-ray crystal structure determination. The access to these peptides has also enabled biological questions concerning these peptides and proteins to be resolved. The review describes different solid-phase methods, which are individually suited for different types of lipopeptides, differing for example in lipidation pattern or amino acid side-chain functionality, and their ligation to proteins. Finally, an example is provided how these peptides can serve to resolve biological aspects of the Ras family GTPases. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:151 / 165
页数:15
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