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蛋白质-蛋白质相互作用的分子胶:迈向新梦想的进展。

Molecular glues for protein-protein interactions: Progressing toward a new dream.

机构信息

Department of Pharmaceutical Chemistry and Small Molecule Discovery Center (SMDC), University of California, San Francisco, San Francisco, CA 94143, USA.

Department of Pharmaceutical Chemistry and Small Molecule Discovery Center (SMDC), University of California, San Francisco, San Francisco, CA 94143, USA.

出版信息

Cell Chem Biol. 2024 Jun 20;31(6):1064-1088. doi: 10.1016/j.chembiol.2024.04.002. Epub 2024 May 2.

Abstract

The modulation of protein-protein interactions with small molecules is one of the most rapidly developing areas in drug discovery. In this review, we discuss advances over the past decade (2014-2023) focusing on molecular glues (MGs)-monovalent small molecules that induce proximity, either by stabilizing native interactions or by inducing neomorphic interactions. We include both serendipitous and rational discoveries and describe the different approaches that were used to identify them. We classify the compounds in three main categories: degradative MGs, non-degradative MGs or PPI stabilizers, and MGs that induce self-association. Diverse, illustrative examples with structural data are described in detail, emphasizing the elements of molecular recognition and cooperative binding at the interface that are fundamental for a MG mechanism of action.

摘要

小分子与蛋白质-蛋白质相互作用的调节是药物发现中发展最快的领域之一。在这篇综述中,我们讨论了过去十年(2014-2023 年)的进展,重点介绍了分子胶(MGs)——单价小分子,通过稳定天然相互作用或诱导新表型相互作用来诱导接近。我们包括了偶然发现和合理发现,并描述了用于识别它们的不同方法。我们将化合物分为三类:降解性 MGs、非降解性 MGs 或 PPI 稳定剂以及诱导自组装的 MGs。详细描述了具有结构数据的不同、有代表性的例子,强调了分子识别和界面上协同结合的基本元素,这些元素是 MG 作用机制的基础。

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