自噬
背景(考古学)
溶酶体
药物发现
细胞生物学
液泡
计算生物学
蛋白质降解
拟肽
药品
生物
化学
生物信息学
生物化学
药理学
肽
细胞凋亡
细胞质
酶
古生物学
作者
Honggang Xiang,Mi Zhou,Yan Li,Lu Zhou,Renxiao Wang
标识
DOI:10.1016/j.apsb.2023.07.016
摘要
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.
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