Transient light-induced intracellular oxidation revealed by redox biosensor

被引:7
|
作者
Kolossov, Vladimir L. [1 ]
Beaudoin, Jessica N. [1 ,2 ]
Hanafin, William P. [1 ]
DiLiberto, Stephen J. [1 ,2 ]
Kenis, Paul J. A. [1 ,3 ]
Gaskins, H. Rex [1 ,2 ,4 ,5 ]
机构
[1] Univ Illinois, Inst Genom Biol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Anim Sci, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Pathobiol, Urbana, IL 61801 USA
[5] Univ Illinois, Div Nutr Sci, Urbana, IL 61801 USA
基金
美国国家卫生研究院;
关键词
Live cell imaging; Redox-sensitive probe; Green fluorescent protein (GFP); Glutathione; Light-induced oxidation; FLUORESCENT PROTEIN INDICATORS; ENDOPLASMIC-RETICULUM; CELL; STRESS; MITOCHONDRIAL; ENVIRONMENT; PROBES; STATE;
D O I
10.1016/j.bbrc.2013.09.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have implemented a ratiometric, genetically encoded redox-sensitive green fluorescent protein fused to human glutaredoxin (Grx1-roGFP2) to monitor real time intracellular glutathione redox potentials of mammalian cells. This probe enabled detection of media-dependent oxidation of the cytosol triggered by short wavelength excitation. The transient nature of light-induced oxidation was revealed by time-lapse live cell imaging when time intervals of less than 30 s were implemented. In contrast, transient ROS generation was not observed with the parental roGFP2 probe without Grx1, which exhibits slower thioldisulfide exchange. These data demonstrate that the enhanced sensitivity of the Grx1-roGFP2 fusion protein enables the detection of short-lived ROS in living cells. The superior sensitivity of Grx1-roGFP2, however, also enhances responsiveness to environmental cues introducing a greater likelihood of false positive results during image acquisition. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:517 / 521
页数:5
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