活性氧
荧光
荧光团
化学
猝灭(荧光)
生物物理学
氧气
二价
细胞凋亡
光化学
程序性细胞死亡
下调和上调
体内
双重角色
生物化学
生物
组合化学
有机化学
生物技术
物理
基因
量子力学
作者
Yueqi Wang,Changjian Li,Jiaming Zhuo,Hui Hui,Bing Zhou,Jie Tian
标识
DOI:10.1007/s11307-022-01774-6
摘要
Ferroptosis, a programmed cell death modality, is an iron-dependent, non-apoptosis pathway that is characterized by the upregulation of divalent iron and reactive oxygen species (ROS) levels. However, the sensitive and rapid detection to track changes in ferroptosis is challenging, partially due to the lack of methods for monitoring the Fe(II) accumulation and ROS generation.Herein, we reported a dual-reaction fluorescent probe DR-1 with turn-on response, which realized the simultaneous visualizing of Fe(II) and ROS with a single probe. The structure of fluorescence quenching group and turn-on fluorophore constitute a double switch for DR-1, which increases its specificity and stability.During ferroptotic cell death, the upregulation of ROS levels led to the cleavage of quenching group of DR-1, and the aggregation of Fe(II) resulting in fluorescence recovery.Overall, this study provides a new dual-reaction probe that shows the great potential to explore the mechanism of ferroptosis in vitro and in vivo by fluorescence imaging.
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