Can self‐inhibitory peptides be derived from the interfaces of globular protein–protein interactions?

生物信息学 对接(动物) 蛋白质-蛋白质相互作用 球状蛋白 计算生物学 背景(考古学) 化学 生物 生物化学 医学 基因 古生物学 护理部
作者
Nir London,Barak Raveh,Dana Movshovitz‐Attias,Ora Schueler‐Furman
出处
期刊:Proteins [Wiley]
卷期号:78 (15): 3140-3149 被引量:152
标识
DOI:10.1002/prot.22785
摘要

Abstract In this study, we assess on a large scale the possibility of deriving self‐inhibitory peptides from protein domains with globular architectures. Such inhibitory peptides would inhibit interactions of their origin domain by mimicking its mode of binding to cognate partners, and could serve as promising leads for rational design of inhibitory drugs. For our large‐scale analysis, we analyzed short linear segments that were cut out of protein interfaces in silico in complex structures of protein–protein docking Benchmark 3.0 and CAPRI targets from rounds 1–19. Our results suggest that more than 50% of these globular interactions are dominated by one short linear segment at the domain interface, which provides more than half of the original interaction energy. Importantly, in many cases the derived peptides show strong energetic preference for their original binding mode independently of the context of their original domain, as we demonstrate by extensive computational peptide docking experiments. As an in depth case study, we computationally design a candidate peptide to inhibit the EphB4–EphrinB2 interaction based on a short peptide derived from the G‐H loop in EphrinB2. Altogether, we provide an elaborate framework for the in silico selection of candidate inhibitory molecules for protein–protein interactions. Such candidate molecules can be readily subjected to wet‐laboratory experiments and provide highly promising starting points for subsequent drug design. Proteins 2010. © 2010 Wiley‐Liss, Inc.
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