偶氮苯
化学
基因敲除
连接器
小分子
泛素连接酶
蛋白质水解
蛋白质降解
融合蛋白
K562细胞
靶蛋白
生物物理学
泛素
分子
生物化学
细胞
有机化学
生物
操作系统
基因
酶
细胞凋亡
计算机科学
重组DNA
作者
Yuhui Jin,Mengchen Lu,Yan Wang,Wen-Xin Shan,Xuan‐Yu Wang,Qidong You,Zhengyu Jiang
标识
DOI:10.1021/acs.jmedchem.9b02058
摘要
Reversibly altering endogenous protein levels are persistent issues. Herein, we designed photoswitchable azobenzene-proteolysis targeting chimeras (Azo-PROTACs) by including azobenzene moieties between ligands for the E3 ligase and the protein of interest. Azo-PROTACs are light-controlled small-molecule tools for protein knockdown in cells. The light-induced configuration change can switch the active state to induce protein degradation activity, which can be reversely controlled by light exposure in intact cells. We compared the protein degradation abilities of Azo-PROTACs with different configurations and linker lengths. Using the stable form with the best degradation ability against the BCR-ABL fusion and ABL proteins in myelogenous leukemia K562 cells, we showed that Azo-PROTAC combines the potent protein knockdown and facile cell uptake properties of the small-molecule PROTAC with a reversible photoswitchability, offering a promising chemical knockdown strategy based on the light-induced reversible on/off properties.
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