化学
抽象
荧光
级联
计算生物学
活性氧
生物化学
细胞
激进的
程序性细胞死亡
氢原子萃取
氧化磷酸化
费斯特共振能量转移
脂质过氧化
脂质积聚
脂质氧化
生物物理学
纳米技术
生物传感器
理想(伦理)
细胞生物学
钥匙(锁)
组合化学
过氧化氢
作者
Cankun Li,Cheng Yao,Ruiqi Su,Yanyan Deng,Chunchun Jiang,Yuyang Zhang,Jiamu Wei,Lei Li,Linyan Huang,Yubo Lin,Guangbo Ge,Suhua Qi,Xuhong Qian,Xiao Luo,Youjun Yang
摘要
Ferroptosis is an Fe 2+ -dependent and lipid peroxidation-mediated regulated cell death. Its early detection is critical for diagnosis and timely intervention. Lipid hydrogen abstraction is the initiation step of the “lipid peroxidation-ferroptosis” cascade and an ideal target for early detection of ferroptosis. We developed the first set of fluorogenic probes for lipid H-abstraction, i.e., LHA 585 for red, LHA675 for deep-red, and LHA930 for near-infrared. The key to their design is the use of 4-phenyl-3-methylbut-2-enyl, a close mimic of the polyunsaturated lipid, to specifically detect the highly oxidative radicals involved in ferroptosis. Notably, LHA585 yielded a fluorescence turn-on ca. 8 h earlier than the current gold-standard probe in an in vitro OGD/R model, highlighting its superiority for early detection of ferroptosis. While LHA585/675 is intended for in vitro studies, LHA930 was feasible for in vivo ferroptosis detection. Collectively, these findings establish LHA s as a robust advance for ferroptosis sensing, enabling in-depth mechanistic studies of lipid-peroxidation-driven cell death.
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