蛋白酶体
蛋白质降解
泛素
小分子
蛋白质水解
基因敲除
细胞生物学
RNA干扰
融合蛋白
化学
小干扰RNA
功能(生物学)
生物
生物化学
核糖核酸
基因
酶
重组DNA
作者
Eun Ryoung Jang,Wooin Lee,Kyung Bo Kim
标识
DOI:10.1002/9780470559277.ch090242
摘要
Abstract In recent years, small interference RNAs (siRNAs) have greatly enhanced our understanding of protein functions by allowing knockdown of targeted proteins at the mRNA level. Similarly, in an effort to achieve degradation of targeted proteins at the post‐translational level, chimeric small molecules called “PROTACs” (PROteolysis TArgeting Chimeric molecules) have been developed. The PROTAC approach utilizes chimeric small molecules which recruit targeted proteins to the ubiquitin‐proteasome pathway, a major intracellular protein degradation system. Unlike conventional small molecules that bind to protein and inhibit its function, the PROTAC approach induces destruction of target protein via the ubiquitin‐proteasome system. This article presents a typical strategy for PROTAC design and preparation and biological characterization. Curr. Protoc. Chem Biol . 2:71‐87. © 2010 by John Wiley & Sons, Inc.
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