Fluorogenic Probe Using a Mislow-Evans Rearrangement for Real-Time Imaging of Hydrogen Peroxide

被引:48
作者
Pham, Dianne [1 ]
Basu, Upamanyu [1 ]
Pohorilets, Ivanna [1 ]
St Croix, Claudette M. [2 ]
Watkins, Simon C. [2 ]
Koide, Kazunori [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, 219 Parkman Ave, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Cell Biol, Ctr Biol Imaging, 3500 Terrace St, Pittsburgh, PA 15261 USA
基金
美国国家科学基金会;
关键词
fluorescent probe; oxidation; peroxides; selenium; sigmatropic rearrangement; FLUORESCENT-PROBES; ORGANOSELENIUM CHEMISTRY; ALLYLIC SULFOXIDES; OXIDATIVE BURST; SINGLET OXYGEN; NADPH-OXIDASE; LIVING CELLS; NITRIC-OXIDE; TURN-ON; H2O2;
D O I
10.1002/anie.202007104
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen peroxide (H2O2) mediates the biology of wound healing, apoptosis, inflammation, etc. H2O2 has been fluorometrically imaged with protein- or small-molecule-based probes. However, only protein-based probes have afforded temporal insights within seconds. Small-molecule-based electrophilic probes for H2O2 require many minutes for a sufficient response in biological systems. Here, we report a fluorogenic probe that selectively undergoes a [2,3]-sigmatropic rearrangement (seleno-Mislow-Evans rearrangement) with H2O2, followed by acetal hydrolysis, to produce a green fluorescent molecule in seconds. Unlike other electrophilic probes, the current probe acts as a nucleophile. The fast kinetics enabled real-time imaging of H2O2 produced in endothelial cells in 8 seconds (much earlier than previously shown) and H2O2 in a zebrafish wound healing model. This work may provide a platform for endogenous H2O2 detection in real time with chemical probes.
引用
收藏
页码:17435 / 17441
页数:7
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