生物正交化学
化学
共价键
弹头
串联
组合化学
化学生物学
前药
生物结合
丙烯酰胺
扁桃体
生物化学
小分子
级联反应
点击化学
荧光
靶蛋白
结合
生物物理学
化学合成
纳米技术
动态共价化学
共价结合
作者
Yan Huang,Miao Liu,Dongguang Fan,Fan Xu,Fushuang Xiang,Qingqiang Min,Xingyue Ji
摘要
Precisely controlling the activation of covalent inhibitors through the caging and decaging of their reactive warheads is pivotal, yet this strategy is rarely pursued due to its formidable technical challenges. In this contribution, we report a novel tandem bioorthogonal retro-Cope and Cope elimination designed for efficient and selective activation of the covalent inhibitors bearing an acrylamide or vinylsulfonamide warhead in live cells. Notably, this strategy can be simultaneously tailored to coactivate both the covalent inhibitor and a fluorescent reporter, enabling real-time monitoring of prodrug activation. We successfully demonstrate the proof of concept through on-demand activation of two distinct EGFR covalent inhibitors and a BRD4-targeting molecular glue in live cells. This approach allows precise control over antiproliferative activity or induced protein degradation exclusively upon triggering via the tandem bioorthogonal reaction. We anticipate that this methodology will open new avenues for the selective delivery and controlled activation of covalent inhibitors, with broad potential in chemical biology and targeted therapy.
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