Azo-PROTAC: Novel Light-Controlled Small-Molecule Tool for Protein Knockdown

被引:122
作者
Jin, Yu-Hui [1 ,2 ,3 ]
Lu, Meng-Chen [1 ,2 ,3 ]
Wang, Yan [1 ,2 ,3 ]
Shan, Wen-Xin [1 ,2 ,3 ]
Wang, Xuan-Yu [3 ]
You, Qi-Dong [1 ,2 ,3 ]
Jiang, Zheng-Yu [1 ,2 ,3 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, State Key Lab Nat Med, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Sch Pharm, Jiang Key Lab Drug Design & Optimizat, Nanjing 210009, Peoples R China
[3] China Pharmaceut Univ, Sch Pharm, Dept Med Chem, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
OPTICAL CONTROL; SPATIOTEMPORAL CONTROL; PROTEASOME INHIBITORS; PHOTOCHROMIC AGONIST; IN-VIVO; DEGRADATION; RECEPTOR; PROTEOLYSIS; GLUTAMATE; DESIGN;
D O I
10.1021/acs.jmedchem.9b02058
中图分类号
R914 [药物化学];
学科分类号
100701 ;
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.
引用
收藏
页码:4644 / 4654
页数:11
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