An ESIPT-based fluorescent probe with fast-response for detection of hydrogen sulfide in mitochondria

被引:32
作者
Du, Yuting [1 ]
Wang, Hongliang [1 ]
Zhang, Ting [1 ]
Wen, Wei [1 ]
Li, Zhiying [1 ]
Bi, Minjie [1 ]
Liu, Juan [1 ]
机构
[1] Xinzhou Teachers Univ, Dept Chem, Xinzhou 034000, Shanxi, Peoples R China
关键词
Fluorescent probe; Hydrogen sulfide; Excited-state intramolecular proton transfer; Mitochondria-targeting; INTRAMOLECULAR PROTON-TRANSFER; SENSITIVE DETECTION; RAPID DETECTION; H2S; SULFUR; GASOTRANSMITTERS; ANGIOGENESIS; PERFORMANCE; ABSORPTION; DESIGN;
D O I
10.1016/j.saa.2021.120390
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Excited-state intramolecular proton transfer (ESIPT) has recently received considerable attention due to its dual fluorescent changes and large Stokes shift. Hydrogen sulfide (H2S) is a gas signal molecule that plays important roles in modulating the functions of different systems. Herein, by modifying 2-(2-hydroxyphenyl) benzothiazole (HBT) scaffold, a novel near-infrared mitochondria-targeted fluorescent probe HBTP-H2S has been rationally designed based on excited-state intramolecular proton transfer (ESIPT) effect. The nucleophilic addition reaction of the H2S with probe HBTP-H2S caused the break of the conjugated skeleton, resulting the shifting of maximum emission peak from 658 nm to 470 nm. HBTP-H2S showed fast-response response time, good selectivity and a large Stokes shift (188 nm) toward H2S. Most importantly, inspired by the inherent advantages of the probe, HBTP-H2S was successfully employed to monitor mitochondrial H2S in HepG2 cells. (C) 2021 Published by Elsevier B.V.
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收藏
页数:7
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