相互作用体
化学
蛋白质水解
热休克蛋白
格尔德霉素
蛋白质稳态
蛋白质降解
热休克蛋白70
嵌合体(遗传学)
细胞生物学
伴侣(临床)
生物化学
热休克蛋白90
酶
生物
病理
基因
医学
作者
Jinyun Dong,Furong Ma,Mao-Hua Cai,Fei Cao,Haobin Li,Hui Liang,Yulong Li,Guangyu Ding,Juan Li,Xiangdong Cheng,Jiang‐Jiang Qin
标识
DOI:10.1021/acs.jmedchem.4c01518
摘要
Targeted protein degradation (TPD) is an emerging therapeutic paradigm aimed at eliminating the disease-causing protein with aberrant expression. Herein, we report a new approach to inducing intracellular glutathione peroxidase 4 (GPX4) protein degradation to trigger ferroptosis by bridging the target protein to heat shock protein 90 (HSP90), termed HSP90 interactome-mediated proteolysis targeting chimera (HIM-PROTAC). Different series of HIM-PROTACs were synthesized and evaluated, and two of them, GDCNF-2/GDCNF-11 potently induced ferroptosis via HSP90-mediated ubiquitin-proteasomal degradation of GPX4 in HT-1080 cells with DC
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