Ebadi Pirouz, Stratton Caleb M, Olsen Shaun K
Department of Biochemistry & Structural Biology, and Greehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Department of Biochemistry & Structural Biology, and Greehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Trends Biochem Sci. 2025 Sep 11. doi: 10.1016/j.tibs.2025.07.009.
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.
泛素-蛋白酶体系统(UPS)是蛋白质周转和信号传导的核心调节因子,其中E3泛素连接酶赋予底物特异性和链型控制。最近的进展揭示了E3连接酶的新机制类别,并扩展了我们对其在包括癌症、神经退行性疾病和免疫功能障碍在内的疾病中作用的理解。这些见解推动了靶向蛋白质降解策略的发展,该策略利用UPS消除与疾病相关的蛋白质。诸如蛋白酶靶向嵌合体(PROTACs)、分子胶和基于抗体的降解剂等方法正在拓宽可成药蛋白质组。尽管取得了这一进展,但关键挑战仍然存在,包括E3连接酶多样性有限、降解剂递送困难和耐药机制。本综述概述了E3连接酶生物学和治疗性降解的最新进展,强调了扩展和完善UPS靶向干预措施的机会。