合成修饰蛋白质表面,介导诱导接近药理学。

IF 4.1 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RSC medicinal chemistry Pub Date : 2024-08-09 DOI:10.1039/D4MD00388H
Lyn H. Jones
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引用次数: 0

摘要

分子粘合剂和双功能小分子(如靶向蛋白质降解剂)可诱导蛋白质接近,从而介导功能增益药理学。本文介绍了合成操纵蛋白质表面以创建新蛋白质的新兴技术,以及用于蛋白质内部和之间表面标记的共价化学探针的开发。配体引导的蛋白质表面修饰策略有可能增强诱导接近药理学工具包并扩大可用药的蛋白质组,本论文探讨了未来的机遇和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synthetic modification of protein surfaces to mediate induced-proximity pharmacology

Molecular glues and bifunctional small molecules, such as targeted protein degraders, induce protein proximity to mediate gain-of-function pharmacology. Emerging technologies that synthetically manipulate protein surfaces to create neoproteins, and the development of covalent chemical probes for intra- and inter-protein surface labeling are described. Ligand-directed protein surface modification strategies have the potential to enhance the induced-proximity pharmacology toolkit and expand the druggable proteome, and this Opinion considers the opportunities and challenges that lie ahead.

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CiteScore
5.80
自引率
2.40%
发文量
129
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