泛素
可药性
泛素连接酶
泛素蛋白连接酶类
调节器
DNA连接酶
计算生物学
底物特异性
生物
蛋白质降解
细胞生物学
免疫系统
DDB1型
负调节器
泛素类
生物信息学
机制(生物学)
蛋白酶体
生物化学
卡林
作者
Pirouz Ebadi,Caleb M. Stratton,Shaun K. Olsen
标识
DOI:10.1016/j.tibs.2025.07.009
摘要
The ubiquitin-proteasome system (UPS) is a central regulator of protein turnover and signaling, with E3 ubiquitin ligases conferring substrate specificity and chain-type control. Recent advances have revealed new mechanistic classes of E3 ligases and expanded our understanding of their roles in disease, including cancer, neurodegeneration, and immune dysfunction. These insights have fueled the development of targeted protein degradation strategies that harness the UPS to eliminate disease-associated proteins. Approaches such as proteolysis-targeting chimeras (PROTACs), molecular glues, and antibody-based degraders are broadening the druggable proteome. Despite this progress, key challenges remain, including limited E3 ligase diversity, difficulties in degrader delivery, and resistance mechanisms. This review outlines recent advances in E3 ligase biology and therapeutic degradation, emphasizing opportunities to expand and refine UPS-targeted interventions.
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