小脑
泛素连接酶
化学
泛素
蛋白酶体
生物物理学
细胞生物学
降级(电信)
蛋白质降解
泛素蛋白连接酶类
机制(生物学)
DNA连接酶
HEK 293细胞
三元络合物
生物化学
蛋白质结构
纳米技术
胶水
蛋白质亚单位
血浆蛋白结合
半胱氨酸
蛋白质水解
计算生物学
内质网相关蛋白降解
作者
Gerasimos Langousis,Pablo Gaínza,Moritz Hunkeler,Despoina Kapsitidou,Etienne J. Donckèle,Stefano Annunziato,L. Wiedmer,Katherine F. M. Jones,Bradley DeMarco,Cynthia Quan,R.D. Bunker,Kevin J. Lumb,Bernhard Fasching,John C. Castle,Sharon A. Townson,Débora Bonenfant
标识
DOI:10.1038/s41467-025-65094-3
摘要
Cereblon (CRBN) is an E3 ubiquitin ligase widely harnessed for targeted protein degradation (TPD). We report the discovery of a molecular glue degrader (MGD), MRT-31619, that drives homo-dimerization of CRBN and promotes its fast, potent, and selective degradation by the ubiquitin proteasome system. Interestingly, the cryo-electron microscopy (cryo-EM) structure of the CRBN homodimer reveals a unique mechanism whereby two molecular glues assemble into a helix-like structure and drive ternary complex formation by mimicking a neosubstrate G-loop degron. This CRBN chemical knockout offers a valuable tool to elucidate the molecular mechanism of MGDs, to investigate its endogenous substrates and understand their physiological roles.
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