Department of Chemistry, Pohang University of Science and Technology, Pohang 790-784, South Korea.
Department of Chemistry, Pohang University of Science and Technology, Pohang 790-784, South Korea; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN 46032, United States.
Curr Opin Chem Biol. 2015 Feb;24:38-47. doi: 10.1016/j.cbpa.2014.10.023. Epub 2014 Nov 15.
α-Helices are the most common protein secondary structure and play a key role in mediating many protein-protein interactions (PPIs) by serving as recognition motifs. Given that aberrant α-helix-mediated PPIs are linked to various disease states, targeting such interactions with small-molecules represents an attractive strategy to develop therapeutic candidates for the related diseases. Over the last decade, significant efforts have been directed toward developing α-helix mimetic small-molecules that can modulate α-helix-mediated PPIs. In this review, we will highlight recent advances in the development of non-peptidic, small-molecule α-helix mimetics with a focus on library synthesis and screening methods to efficiently discover small-molecule α-helix mimetics.
α-螺旋是最常见的蛋白质二级结构,通过充当识别基序在介导许多蛋白质-蛋白质相互作用 (PPIs) 中发挥关键作用。鉴于异常的α-螺旋介导的 PPI 与各种疾病状态有关,因此用小分子靶向这些相互作用代表了开发相关疾病治疗候选物的一种有吸引力的策略。在过去的十年中,人们已经做出了巨大的努力来开发可以调节α-螺旋介导的 PPI 的α-螺旋模拟小分子。在这篇综述中,我们将重点介绍非肽类小分子α-螺旋模拟物的最新进展,以及用于有效发现小分子α-螺旋模拟物的文库合成和筛选方法。