Redox Biology · 2022 · 53 citations · 21 references
Life SciencesBiochemistryMolecular BiologyEnzymologyMolecular ImagingProtein BiochemistryDisulfide Bond FormationMolecular Probe DevelopmentSulfur ChemistrySulfur Compound AnalysisSulfur CompoundsChemical PropertiesCysteine-related Sulfur CompoundsDisulfide Bond Isomerase ActivityDisulfide Reductase ActivityPhysical PropertiesProtein Disulfide IsomeraseSelectivitySulfur Compound Detection
Fluorescent probes are useful tools for the detection of sulfane sulfurs in biological systems. In this work, we report the development of SSP4, a widely used probe generated in our laboratory. We describe its evolution, preparation, and physical/chemical properties. Fluorescence analyses of SSP4 determined its high selectivity and sensitivity to sulfane sulfurs, even with the interfering presence of other species, such as amino acids and metal ions. Protocols for using SSP4 in a relatively quick and simple manner for the detection of persulfidated proteins, including papain, BSA, and GAPDH were developed. The method was then applied to human protein disulfide isomerase (PDI), leading to the discovery that persulfidation can occur at PDI's non-active site cysteines, and that PDI reductase activity is affected by sulfane sulfur treatment. Protocols for using SSP4 for the bioimaging of exogenous and endogenous sulfane sulfurs in different -cell lines were also established. These results should guide further applications of SSP4.
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Polysulfides Link H <sub>2</sub> S to Protein Thiol Oxidation
Romy Greiner, Zoltán Pálinkás, Katrin Bäsell et al. · Antioxidants and Redox Signaling · 2013 · 459 citations · Full text