小脑
泛素连接酶
泛素
化学
计算生物学
化学生物学
基因敲除
蛋白质降解
泛素蛋白连接酶类
小分子
HEK 293细胞
DNA连接酶
生物化学
细胞生物学
靶蛋白
细胞
赖氨酸
天然化学连接
血浆蛋白结合
蛋白质-蛋白质相互作用
蛋白质稳定性
细胞培养
组合化学
鉴定(生物学)
药物发现
纳米技术
生物
细胞生长
德隆
蛋白质设计
分子生物学
作者
Rebecca Stevens,Kwok-Ho Chan,Alice Moore,Sam Hardie,Glenn A. Burley,Jennifer J. Knickelbine,Kristin M. Riching,Agnieszka Konopacka,Markus A. Queisser,Afjal H. Miah
标识
DOI:10.1021/acschembio.6c00377
摘要
HaloTags have emerged as versatile tools for protein labeling, investigating target biology, and facilitating targeting protein degradation using synthetic ligands called HaloPROTACs. These chemical tools are heterobifunctional molecules consisting of a chloroalkane derivative linked to E3 ubiquitin ligase-recruiting moieties to artificially induce proximity between the ligase and target protein of interest fused to the HaloTag construct. Through this induced proximity, HaloPROTACs can facilitate temporal- and dose-dependent degradation of target proteins, enabling efficient cellular protein knockdown without the need for target-specific ligands. In this study, we developed cereblon (CRBN)-recruiting HaloPROTACs through the use of plate-based high-throughput synthesis and direct-to-biology screening. We evaluated over 100 structurally diverse CRBN HaloPROTACs in an FAK-tagged cell line, resulting in the identification of highly potent tools. Notably, HaloPROTACs incorporating dihydrouracil CRBN binders exhibited superior potency and selectivity compared with their IMiD-based counterparts. These newly developed CRBN-based HaloPROTACs represent a valuable addition to the existing HaloPROTAC toolkit, offering enhanced capabilities for advancing research on targeted protein degradation.
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