光电开关
蛋白质降解
泛素连接酶
偶氮苯
靶蛋白
泛素
FKBP公司
细胞生物学
蛋白质水解
化学
生物
生物化学
分子
光化学
基因
酶
有机化学
作者
Martin Reynders,Dirk Trauner
标识
DOI:10.1007/978-1-0716-1665-9_17
摘要
Proteolysis Targeting Chimeras (PROTACs) are a promising technology to degrade specific target proteins. As bifunctional small molecules, PROTACs induce the ternary complex formation between an E3 ligase and a protein of interest (POI), leading to polyubiquitylation and subsequent proteasomal degradation of the protein in a catalytic fashion. We have developed a strategy to control PROTACs with the spatiotemporal precision of light, which led to light-activated versions, termed PHOTACs (PHOtochemically TArgeted Chimeras). By incorporating an azobenzene photoswitch into the PROTAC, we can reversibly control degradation of the POI, as demonstrated for BRD2-4 and FKBP12. Here, we describe our modular approach and the application of PHOTACs for the optical control of protein levels in detail. PHOTACs hold promise as both research tools and precision pharmaceutics.
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