Targeting Protein-Protein Interfaces Using Macrocyclic Peptides

被引:51
|
作者
Gao, Meng [1 ]
Cheng, Kui [1 ]
Yin, Hang [1 ,2 ]
机构
[1] Tsinghua Univ, Dept Chem, Ctr Basic Mol Sci, Beijing 100082, Peoples R China
[2] Univ Colorado, Dept Chem & Biochem, BioFrontiers Inst, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
macrocyclic peptide; protein-protein interface; rational design; inhibitor; SMALL-MOLECULE INHIBITORS; HIV-1; INTEGRASE; HELICAL PEPTIDES; DISCOVERY; DESIGN; POTENT; ANTAGONIST; BINDING; RECOGNITION; ACTIVATION;
D O I
10.1002/bip.22625
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 (PPIs) are critical in numerous biological processes including signaling transduction, function regulations, and disease development. To regulate PPIs has been thought to be challenging due to their highly dynamic and expansive interfacial areas. Nonetheless, successful examples have been reported of targeting PPIs using small molecules, peptides, and proteins. Peptides, especially macrocyclic peptides have proven to be a particularly useful tool to inhibit PPIs for their exquisite potency, stability and selectivity. Herein we review the recent developments of this area of research, focusing on the macrocyclic peptides isolated from natural products, identified from library screening, and rationally designed based on structures, as PPI regulators. (C) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:310 / 316
页数:7
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