Cunningham Anna D, Qvit Nir, Mochly-Rosen Daria
Department of Chemical and Systems Biology, Stanford University, School of Medicine, Stanford, CA 94305-5174, USA.
Department of Chemical and Systems Biology, Stanford University, School of Medicine, Stanford, CA 94305-5174, USA.
Curr Opin Struct Biol. 2017 Jun;44:59-66. doi: 10.1016/j.sbi.2016.12.009. Epub 2017 Jan 4.
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.
蛋白质-蛋白质相互作用对于几乎所有细胞内和细胞外的生物学过程都至关重要。调节蛋白质-蛋白质相互作用是一种以高度选择性方式调节细胞命运的策略。具体而言,肽是抑制蛋白质-蛋白质相互作用的理想候选物,因为它们可以模拟蛋白质表面以有效竞争结合。此外,肽可以通过化学合成获得,并且可以通过化学修饰来稳定。在本综述中,我们概述了用于鉴定抑制蛋白质-蛋白质相互作用的肽的筛选和合理设计方法,以及稳定肽以有效模拟蛋白质表面的方法。此外,我们还讨论了肽在基础研究和治疗目的中调节蛋白质-蛋白质相互作用的最新应用。