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A novel "turn-on" mitochondria-targeting near-infrared fluorescent probe for determination and bioimaging cellular hydrogen sulfide
被引:14
|作者:
Zhao, Xiong-jie
[1
]
Jiang, Yu-ren
[1
]
Li, Yu-ting
[1
]
Yang, Bing-qing
[1
]
Liu, Ce
[1
]
Liu, Zhi-hong
[1
]
机构:
[1] Cent S Univ, Coll Chem & Chem Engn, Dept Pharmaceut Engn, Changsha 410083, Hunan, Peoples R China
基金:
中国国家自然科学基金;
关键词:
NIR fluorescent probe;
Mitochondria-targeting;
Turn-on" response;
Fast response;
Hydrogen sulfide;
LIVING CELLS;
H2S;
SULFUR;
D O I:
10.1016/j.saa.2018.12.046
中图分类号:
O433 [光谱学];
学科分类号:
0703 ;
070302 ;
摘要:
Hydrogen sulfide (H2S) has been regarded as an important gas transmitter playing vital role in cytoprotective processes and redox signaling. It is very meaningful to monitor and analyze it in biosystem for obtaining important physiological and pathological information. Despite numerous fluorescent probes for cellular H2S have been reported in past decades, only a few have capability to detect mitochondria' H2S with near-infrared (NIR) emission. Therefore, a new mitochondria-targeting NIR fluorescent probe (Mito-NSH) for detection of cellular H2S was developed by introducing 2,4-dinitrophenyl ether into a novel dye (Mito-NOH). A large "turn-on" NIR fluorescence response was obtained due to thiolysis of ether to hydroxyl group when Mito-NSH was treated with NaHS. Moreover, Mito-NSH could quantitatively detect H2S at concentration ranging from 0 to 30 mu M with a detection limit of 68.2 nM, and it exerts some superior optical properties, such as large stokes shift (107 nm), highly selectively mitochondria location, fast response and high selectivity to H2S. More impressively, it was successfully applied to imaging exogenous and endogenously generated H2S in living HeLa cells via confocal fluorescence microscopy. (C) 2018 Elsevier B.V. All rights reserved.
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页码:71 / 77
页数:7
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