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

被引:10
|
作者
Xiang, Honggang [1 ]
Zhou, Mi [1 ]
Li, Yan [1 ]
Zhou, Lu [1 ]
Wang, Renxiao [1 ]
机构
[1] Fudan Univ, Sch Pharm, Dept Med Chem, Shanghai 201203, Peoples R China
关键词
Autophagy regulation; Protein-protein interactions; Small-molecule regulators; Drug discovery; SMALL-MOLECULE INHIBITORS; NETWORK; COMPLEX; CANCER; IDENTIFICATION; DIVERSITY; RESOURCE; DISEASE; MODEL; MECHANISMS;
D O I
10.1016/j.apsb.2023.07.016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Autophagy is a cellular process in which proteins and organelles are engulfed in autophago-somal 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 reg-ulators, 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 regu-lators targeting those PPIs. Successful strategies and existing limitations in this field are also discussed.(c) 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:4373 / 4390
页数:18
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