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-SulfoBiotics- SSP4

Item # Unit Size
SB10-10
1 mg

For Research Use Only Products



Storage Condition : -20℃, protect from light
Shipping Condition : Blue Ice
Purity : ≥90.0% (HPLC)
Chemical name: 3',6'-Di(O-thiosalicyl)fluorescein 
M.W.: 604.65
CAS#: N/A


Product Description:

SSP4 (Sulfane Sulfur Probe 4) is a novel fluorescent probe to detect sulfane sulfurs selectively. SSP4 itself is non-fluorescent, but it emits strong green fluorescence when it reacts with sulfane sulfurs. Thus, SSP4 enables high sensitive fluorescence detection and imaging of sulfane sulfurs.

       

        Fig. 1 Reaction of SSP4 with sulfane sulfurs




Fluorescent property:

       

Chemical species of Intravital sulfane sulfur:

       



Selectivity of the SSP4:
       

Experimental example:

Detection of sulfane sulfurs in cells treated with a sulfane sulfur donor or sulfane sulfur quencher.

1) W. Chen, C. Liu, B. Peng, Y. Zhao, A. Pacheco, and M. Xian, “New fluorescent probe for sulfane sulfurs and the application in bioimaging”, Chem. Sci., 2013, 4, 2892.
2) T. Ida, T. Sawa, H. Ihara. Y. Tsuchiya, Y. Watanabe, Y. Kumagai, M. Suematsu, H. Motohashi, S. Fujii, T, Matsunaga, M. Yamamoto, K. Ono, N. O. Devarie-Baez, M. Xian, J. M Fukuto, and T. Akaike, “Reactive cysteine persulfides and S-polythiolation regulate oxidative stress and redox signaling”, Proc Natl Acad Sci U S A., 2014, 111, 7606.
3) E. Marutani, M. Sakaguchi, W. Chen, K. Sasakura, J. Liu, M. Xian, K. Hanaoka, T. Nagano, and F. Ichinose, "Cytoprotective effects of hydrogen sulfide-releasing N-methyl-D-aspartate receptor antagonists mediated by intracellular sulfane sulfur", Med. Chem. Commun., 2014, 5, 1577.
4) M. Sakaguchi, E. Marutani, H-S. Shin, W. Chen, K. Hanaoka, M. Xian, and F. Ichinose, “Sodium Thiosulfate Attenuates Acute Lung Injury in Mice”, Anesthesiology, 2014, 121, 1248
5) Y. Kimura, Y. Toyofuku, S. Koike, N. Shibuya, N. Nagahara, D. Lefer, Y. Ogasawara, and H. Kimura, "Identification of H2S3 and H2S produced by 3-mercaptopyruvate sulfurtransferase in the brain", Nature Scientific Reports., 2015, 5, 14774.
6) E. DeLeon, Y. Gao, E. Huang, M. Arif, N. Arora, A. Divietro, S. Patel, K. Olson, "A case of mistaken identity: are reactive oxygen species actually reactive sulfide species?", Am J Physiol Regul Integr Comp Physiol, 2016, 310(7), R549.
7) P. Yadav, M. Martinov, V. Vitvitsky, J. Seravalli, R. Wedmann, M. Filipovic, and R. Banerjee, "Biosynthesis and Reactivity of Cysteine Persulfides in Signaling", Jounal of the American Chemical Society., 2016, 138, (1), 289.
8)A. Moustafa, Y. Habara, "Reciprocal interaction among gasotransmitters in isolated pancreatic β-cells", Free Radical Biology and Medicine., 2016, 90, 47.
9) A. Moustafa and Y. Habara, "Crosstalk between polysulfide and nitric oxide in rat peritoneal mast cells", Am. J. Physiol. Cell Physiol., (in press)
10) E. R. DeLeon, Y. Gao, E. Huang, M. Arif, N. Arora, A. Divietro, S. Patel, and K. R. Olson , "A case of mistaken identity: are reactive oxygen species actually reactive sulfide species?", American Journal of Physiology: Regulatory, Integrative and Comparative Physiology ., 2015, 310, (7), 549.
11) N. Takahashi, FY Wei, S. Watanabe, M. Hirayama, Y. Ohuchi, A. Fujimura, T. Kaitsuka, I. Ishii, T. Sawa, H. Nakayama, T. Akaike and K. Tomizawa,"Reactive sulfur species regulate tRNA methylthiolation and contribute to insulin secretion", Nucleic Acids Res., 2016, doi: 10.1093/nar/gkw745 .