CCR2型
化学
泛素连接酶
变构调节
G蛋白偶联受体
趋化因子受体
泛素
生物化学
受体
趋化因子受体
蛋白质水解
DNA连接酶
细胞生物学
蛋白质降解
药物发现
计算生物学
细胞内
单核细胞
配体(生物化学)
ATP结合盒运输机
作者
Khaled Essa,Natalia V. Ortiz Zacarı́as,Sascha Röth,Bo‐Tao Xin,Sabine de Winter,Cas van der Horst,Bente T.M. Bleijs,Richard A. de Heiden,Rodanthi Voulgaraki,Elsa Neubert,Huib Ovaa,Erik H.J. Danen,Monique P. C. Mulder,Kévin Moreau,Daan van der Es,Laura H. Heitman
标识
DOI:10.1021/acs.jmedchem.5c02920
摘要
Targeted protein degradation (TPD) is one of the most prominent and rapidly advancing modalities in drug discovery. However, only few degraders have been reported for the membrane-bound G protein-coupled receptors (GPCRs). Therefore, using CC chemokine receptor 2 (CCR2) as a GPCR model, we synthesized potential CCR2 molecular degraders. The putative proteolysis-targeting chimeras (PROTACs) employed an allosteric intracellular CCR2 ligand tethered to commonly used E3 ligase ligands. Among these compounds, LUF7996 (8) demonstrated engagement of both CCR2 and the E3 ligase cereblon and displayed sustained and concentration-dependent degradation of CCR2 over 24 h. Mechanistic studies revealed the reliance of LUF7996 on the lysosomal pathway to induce CCR2 degradation. Finally, LUF7996 (8) efficiently inhibited monocyte migration in a transwell assay. Collectively, the developed assessment workflow led to identification of the first CCR2 molecular degraders and has the potential to expand the repertoire of degraders targeting the pharmacologically rich GPCRs.
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