泛素连接酶
融合蛋白
小分子
蛋白质降解
药物发现
化学基因学
化学
泛素
靶蛋白
细胞生物学
计算生物学
生物化学
化学生物学
生物
重组DNA
基因
作者
Dennis L. Buckley,Kanak Raina,Nicole Darricarrère,John Hines,Jeffrey L. Gustafson,Ian E. Smith,Afjal H. Miah,John D. Harling,Craig M. Crews
标识
DOI:10.1021/acschembio.5b00442
摘要
Small molecule-induced protein degradation is an attractive strategy for the development of chemical probes. One method for inducing targeted protein degradation involves the use of PROTACs, heterobifunctional molecules that can recruit specific E3 ligases to a desired protein of interest. PROTACs have been successfully used to degrade numerous proteins in cells, but the peptidic E3 ligase ligands used in previous PROTACs have hindered their development into more mature chemical probes or therapeutics. We report the design of a novel class of PROTACs that incorporate small molecule VHL ligands to successfully degrade HaloTag7 fusion proteins. These HaloPROTACs will inspire the development of future PROTACs with more drug-like properties. Additionally, these HaloPROTACs are useful chemical genetic tools, due to their ability to chemically knock down widely used HaloTag7 fusion proteins in a general fashion.
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