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Cyanine-based fluorescent probe for highly selective detection of glutathione in cell cultures and live mouse tissues.

Authors
 Jun Yin  ;  Younghee Kwon  ;  Dabin Kim  ;  Dayoung Lee  ;  Gyoungmi Kim  ;  Ying Hu  ;  Ji-Hwan Ryu  ;  Juyoung Yoon 
Citation
 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, Vol.136(14) : 5351-5358, 2014 
Journal Title
 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY 
ISSN
 0002-7863 
Issue Date
2014
MeSH
Animals ; Carbocyanines/chemical synthesis ; Carbocyanines/chemistry* ; Carbocyanines/pharmacokinetics ; Cell Line ; Cells, Cultured ; Female ; Fluorescent Dyes/chemical synthesis ; Fluorescent Dyes/chemistry* ; Fluorescent Dyes/pharmacokinetics ; Glutathione/analysis* ; HeLa Cells ; Humans ; Mice ; Mice, Inbred C57BL ; Tissue Distribution
Abstract
Glutathione (GSH) plays a crucial role in human pathologies. Near-infrared fluorescence-based sensors capable of detecting intracellular GSH in vivo would be useful tools to understand the mechanisms of diseases. In this work, two cyanine-based fluorescent probes, 1 and 2, containing sulfonamide groups were prepared. Evaluation of the fluorescence changes displayed by probe 1, which contains a 2,4-dinitrobenzenesulfonamide group, shows that it is cell-membrane-permeable and can selectively detect thiols such as GSH, cysteine (Cys), and homocysteine (Hcy) in living cells. The response of 1 to thiols can be reversed by treatment with N-methylmaleimide (NMM). Probe 2, which possesses a 5-(dimethylamino)naphthalenesulfonamide group, displays high selectivity for GSH over Cys and Hcy, and its response can be reversed using NMM. The potential biological utility of 2 was shown by its use in fluorescence imaging of GSH in living cells. Furthermore, probe 2 can determine changes in the intracellular levels of GSH modualated by H2O2. The properties of 2 enable its use in monitoring GSH in vivo in a mouse model. The results showed that intravenous injection of 2 into a mouse generates a dramatic image in which strong fluorescence is emitted from various tissues, including the liver, kidney, lung, and spleen. Importantly, 2 can be utilized to monitor the depletion of GSH in mouse tissue cells promoted by excessive administration of the painkiller acetaminophen. The combined results coming from this effort suggest that the new probe will serve as an efficient tool for detecting cellular GSH in animals.
Full Text
http://pubs.acs.org/doi/abs/10.1021/ja412628z
DOI
10.1021/ja412628z
Appears in Collections:
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
5. Research Institutes (연구소) > Research Center for Human Natural Defense System (생체방어연구센터) > 1. Journal Papers
Yonsei Authors
Kwon, Younghee(권영희)
Ryu, Ji Hwan(유지환)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/98465
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