Peptides and peptidomimetics as regulators of protein-protein interactions

被引:110
|
作者
Cunningham, Anna D. [1 ]
Qvit, Nir [1 ]
Mochly-Rosen, Daria [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Chem & Syst Biol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
ABERRANT MITOCHONDRIAL FISSION; KINASE-C; PHAGE DISPLAY; DELTA; INHIBITORS; EXPLORATION; TECHNOLOGY; DELIVERY; REVEALS; INJURY;
D O I
10.1016/j.sbi.2016.12.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein-protein interactions are essential for almost all intracellular and extracellular biological processes. Regulation of protein-protein interactions is one strategy to regulate cell fate in a highly selective manner. Specifically, peptides are ideal candidates for inhibition of protein-protein interactions because they can mimic a protein surface to effectively compete for binding. Additionally, peptides are synthetically accessible and can be stabilized by chemical modifications. In this review, we survey screening and rational design methods for identifying peptides to inhibit protein-protein interactions, as well as methods for stabilizing peptides to effectively mimic protein surfaces. In addition, we discuss recent applications of peptides to regulate protein-protein interactions for both basic research and therapeutic purposes.
引用
收藏
页码:59 / 66
页数:8
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