粒体自噬
化学
帕金
泛素连接酶
泛素
酶
生物化学
蛋白酶
药物发现
细胞生物学
自噬
生物
细胞凋亡
基因
病理
疾病
医学
帕金森病
作者
Arthur F. Kluge,Bharat Lagu,Pranab Maiti,Mahaboobi Jaleel,Michael Webb,Jyoti Malhotra,Ashley Mallat,P. Akhila Srinivas,James E. Thompson
标识
DOI:10.1016/j.bmcl.2018.05.013
摘要
Mitophagy is one of the processes that cells use to maintain overall health. An E3 ligase, parkin, ubiquitinates mitochondrial proteins prior to their degradation by autophagasomes. USP30 is an enzyme that de-ubiquitinates mitochondrial proteins; therefore, inhibiting this enzyme could foster mitophagy. Herein, we disclose the structure-activity relationships (SAR) within a novel series of highly selective USP30 inhibitors. Two structurally similar compounds, MF-094 (a potent and selective USP30 inhibitor) and MF-095 (a significantly less potent USP30 inhibitor), serve as useful controls for biological evaluation. We show that MF-094 increases protein ubiquitination and accelerates mitophagy.
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