Suppr超能文献

通过靶向自噬过程中涉及的蛋白质-蛋白质相互作用来进行药物发现。

Drug discovery by targeting the protein-protein interactions involved in autophagy.

作者信息

Xiang Honggang, Zhou Mi, Li Yan, Zhou Lu, Wang Renxiao

机构信息

Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai 201203, China.

出版信息

Acta Pharm Sin B. 2023 Nov;13(11):4373-4390. doi: 10.1016/j.apsb.2023.07.016. Epub 2023 Jul 20.

Abstract

Autophagy is a cellular process in which proteins and organelles are engulfed in autophagosomal vesicles and transported to the lysosome/vacuole for degradation. Protein-protein interactions (PPIs) play a crucial role at many stages of autophagy, which present formidable but attainable targets for autophagy regulation. Moreover, selective regulation of PPIs tends to have a lower risk in causing undesired off-target effects in the context of a complicated biological network. Thus, small-molecule regulators, including peptides and peptidomimetics, targeting the critical PPIs involved in autophagy provide a new opportunity for innovative drug discovery. This article provides general background knowledge of the critical PPIs involved in autophagy and reviews a range of successful attempts on discovering regulators targeting those PPIs. Successful strategies and existing limitations in this field are also discussed.

摘要

自噬是一种细胞过程,其中蛋白质和细胞器被包裹在自噬体小泡中,并被运输到溶酶体/液泡进行降解。蛋白质-蛋白质相互作用(PPI)在自噬的许多阶段发挥着关键作用,这为自噬调节提供了艰巨但可实现的靶点。此外,在复杂的生物网络背景下,对PPI的选择性调节往往具有较低的产生不良脱靶效应的风险。因此,针对参与自噬的关键PPI的小分子调节剂,包括肽和肽模拟物,为创新药物发现提供了新的机会。本文提供了参与自噬的关键PPI的一般背景知识,并综述了一系列针对这些PPI发现调节剂的成功尝试。还讨论了该领域的成功策略和现有局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0239/10638514/61e1a4a5b6d1/ga1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验