化学
降级(电信)
泛素连接酶
计算生物学
蛋白质降解
小分子
三元络合物
靶蛋白
蛋白质-蛋白质相互作用
血浆蛋白结合
计算机科学
泛素
终端(电信)
生物化学
三元运算
HEK 293细胞
蛋白质稳定性
蛋白质组学
蛋白质水解
钥匙(锁)
细胞生物学
作者
Chenlu Zhang,Xiaokang Jin,Chen Zhou,M. Jamal Jenkins,Isabella A. Riha,Xiaoyu Zhang
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2026-01-29
标识
DOI:10.64898/2026.01.28.702440
摘要
Targeted protein degradation (TPD) is a powerful strategy for controlling protein abundance. Here, we establish FBXO31 as a TPD-competent E3 ligase by exploiting its recognition of C-terminal amide-bearing degrons. Using an amidated Ala-Phe motif as a chemical recruiter, multiple small-molecule binders can be transformed into FBXO31-dependent degraders that induce rapid and potent target degradation. Mechanistic studies confirm FBXO31-mediated ternary complex formation and identify key residues in FBXO31 required for recruiter engagement and target degradation. We further show that an FBXO31-based multi-kinase degrader exhibits a distinct and broader degradation profile than a CRBN-based degrader, highlighting a potentially expanded degradable target space beyond CRBN.
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