化学
热休克蛋白70
免疫沉淀
癌症研究
癌细胞
癌症
计算生物学
生物化学
热休克蛋白
生物
基因
遗传学
作者
Ziqian Wang,Ting Song,Zongwei Guo,Laura Bonnette Uwituze,Yafei Guo,Hong Zhang,Hang Wang,Xiaodong Zhang,Hao Pan,Tong Ji,Fangkui Yin,Sheng Zhou,Jian Dai,Zhichao Zhang
标识
DOI:10.1016/j.ejmech.2021.113452
摘要
Targeting cancer-related Hsp70-Bim protein-protein interactions (PPIs) offers a new strategy for the design of Hsp70 inhibitors. Herein, we discovered a novel Hsp70 inhibitor, S1g-6, based on the established BH3 mimetics. S1g-6 exhibited sub-μM binding affinity toward Hsp70 and selectively disrupted Hsp70-Bim PPI. The target specificity of S1g-6 in situ was validated by affinity-based protein profiling, co-immunoprecipitation, and cell-based shRNA assays. S1g-6 specifically antagonized the ATPase activity of Hsp70 upon recruiting Bim and showed selective apoptosis induction in some cancer cell lines over normal ones through suppression of some oncogenic clients of Hsp70, representing a new class of antitumor candidates. Hsp70-Bim PPI exhibited cancer-dependent role as a potential anti-cancer target.
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