Literature DB >> 24025674

Transient light-induced intracellular oxidation revealed by redox biosensor.

Vladimir L Kolossov1, Jessica N Beaudoin, William P Hanafin, Stephen J DiLiberto, Paul J A Kenis, H Rex Gaskins.   

Abstract

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 30s were implemented. In contrast, transient ROS generation was not observed with the parental roGFP2 probe without Grx1, which exhibits slower thiol-disulfide 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.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  GSH; GSSG; Glutathione; Green fluorescent protein (GFP); Grx1; Light-induced oxidation; Live cell imaging; Redox-sensitive probe; human glutaredoxin 1; oxidized glutathione; redox-sensitive green fluorescent proteins; reduced glutathione; roGFP

Mesh:

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Year:  2013        PMID: 24025674      PMCID: PMC3830497          DOI: 10.1016/j.bbrc.2013.09.011

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  24 in total

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  4 in total

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2.  Ratiometric Imaging of Mitochondrial Hydrogen Peroxide in Aβ42-Mediated Neurotoxicity.

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3.  Inhibition of glutathione synthesis distinctly alters mitochondrial and cytosolic redox poise.

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Journal:  Exp Biol Med (Maywood)       Date:  2014-02-28

4.  Design considerations for open-well microfluidic platforms for hypoxic cell studies.

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