Cited by 173Sulfur Compounds in BiologyRedox biology and oxidative stressSulfur-Based Synthesis Techniques

Thiosulfoxide (sulfane) sulfur: new chemistry and new regulatory roles in biology

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Toohey, John, Cooper, Arthur·2014·Molecules

Abstract

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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Crossref · 10.3390/molecules190812789

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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
Venue
Molecules
Publisher
MDPI AG
Published
2014-08-21
Volume
19
Issue
8
Pages
12789-12813
ISSN
1420-3049 (ISSN-L)
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
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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