Thiosulfoxide (sulfane) sulfur: new chemistry and new regulatory roles in biology
Open accessAbstract
The understanding of sulfur bonding is undergoing change. Old theories on hypervalency of sulfur and the nature of the chalcogen-chalcogen bond are now questioned. At the same time, there is a rapidly expanding literature on the effects of sulfur in regulating biological systems. The two fields are inter-related because the new understanding of the thiosulfoxide bond helps to explain the newfound roles of sulfur in biology. This review examines the nature of thiosulfoxide (sulfane, S0) sulfur, the history of its regulatory role, its generation in biological systems, and its functions in cells. The functions include synthesis of cofactors (molybdenum cofactor, iron-sulfur clusters), sulfuration of tRNA, modulation of enzyme activities, and regulating the redox environment by several mechanisms (including the enhancement of the reductive capacity of glutathione). A brief review of the analogous form of selenium suggests that the toxicity of selenium may be due to over-reduction caused by the powerful reductive activity of glutathione perselenide.
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Sulfur atoms with valence 0 or -1 are called sulfane sulfur and are present not only in S8 but also in polysulfide, polythionate and other sulfur compounds.
“These sulfur atoms with valence 0 or -1 are called sulfane sulfur and are present not only in S8 but also in polysulfide, polythionate and other sulfur compounds [43,45].”
From On the chemical biology of the nitrite/sulfide interaction (2015) · cites this paper as [45]
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References 133 · Cited by 173
- Authors
- Toohey, J., & Cooper, A.
- Affiliations
- Cytoregulation Research, Elgin, ON K0G1E0, Canada
- New York Medical College (US)
- Corresponding author
- Toohey, John
- ORCID
- Cooper, Arthur
- Venue
- Molecules
- Publisher
- MDPI AG
- Published
- 2014-08-21
- Volume
- 19
- Issue
- 8
- Pages
- 12789-12813
- ISSN
- 1420-3049 (ISSN-L)
- PMC
- PMC4170951
- OpenAlex
- W1966039102
- Cited by
- 173
- References
- 133
- Citations by year
- 2026: 6 · 2025: 17 · 2024: 9 · 2023: 12 · 2022: 18 · 2021: 10 · 2020: 20 · 2019: 16 · 2018: 15 · 2017: 20 · 2016: 14 · 2015: 12 · 2014: 4
- FWCI
- 1.43
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecules (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Touro Scholar (Touro College) (submittedVersion, cc-by)
- Touro Scholar (Touro College) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK 16739, R01DK016739)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Sulfur Compounds in Biology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Physical Sciences › Chemistry › Organic Chemistry › Sulfur-Based Synthesis Techniques
- Keywords
- sulfane sulfur, sulfur bonding, hypervalent sulfur, molybdenum cofactor, iron-sulfur clusters, enzyme activity modulation, glutathione, redox regulation, selenium toxicity
- MeSH terms
- Animals, Antioxidants, Humans, Oxidation-Reduction, Sulfoxides, Biosynthetic Pathways
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