期刊
REDOX BIOLOGY
卷 56, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.redox.2022.102433
关键词
SSP4; Sulfane sulfurs; Fluorescent probe; S-persulfidation
资金
- NSF [CHE2100870]
- NIH [R01GM125968, R35HL135775, 5U01HL143365]
- American Society of Hematology Scholar Award
- Ministry of Edu- cation, Culture, Sports, Science and Technology (MEXT) , Japan [18H05277, 21H05258, 21H05263, 22K19397, 19K07554, 22K06893]
- Japan Science and Technology Agency (JST) , CREST Grant, Japan [JPMJCR2024]
The fluorescent probe SSP4 exhibits high selectivity and sensitivity to sulfane sulfurs in biological systems, even in the presence of interfering species. Protocols for detecting persulfidated proteins and bioimaging sulfane sulfurs have been developed using SSP4, leading to the discovery of new findings in the field.
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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