泛素连接酶
蛋白质降解
小分子
靶蛋白
泛素
化学生物学
计算生物学
药物发现
细胞生物学
配体(生物化学)
化学基因学
三元络合物
基因敲除
化学
生物
作者
Andrew J. Tao,Gillian E. Gadbois,Stanley A. Buczynski,Fleur M. Ferguson
标识
DOI:10.1016/j.cbpa.2021.102114
摘要
Targeted protein degraders are heterobifunctional small molecules that link a target ligand or bait to an E3-ligase binder via a chemical spacer. Upon entering the cell, these ligands trigger the formation of a ternary complex between the target protein, degrader and E3-ligase, which leads to target polyubiquitination and proteasomal degradation. In recent years, TPD has expanded rapidly as a field, becoming the modality of choice in drug discovery and chemical probe development. This has been driven by the unique pharmacology of these molecules, which allows for fast and reversible knockdown of the target protein. Recent studies have demonstrated that degraders with specificity for a defined subpopulation of a protein-of-interest can be developed, giving rise to the emerging concept of protein state-specific targeting. In this article, we review advances towards developing degraders that differentiate between target protein subpopulations based on their; activation state, oligomerization state, cellular localization state, and cell type.
科研通智能强力驱动
Strongly Powered by AbleSci AI