Xiang Honggang, Zhou Mi, Li Yan, Zhou Lu, Wang Renxiao
Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai 201203, China.
Acta Pharm Sin B. 2023 Nov;13(11):4373-4390. doi: 10.1016/j.apsb.2023.07.016. Epub 2023 Jul 20.
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.
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。