Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a22a195b4f18a3ae

Jump to content

Persulfide

From Wikipedia, the free encyclopedia
Cysteine hydropersulfide (top) and glutathione hydropersulfide (bottom), the two most physiologically relevant persulfide species. The additional sulfanyl group is marked in orange.

In chemistry, hydropersulfide refers to the functional group R-S-S-H.[1][2] The anionic form of a hydropersulfide is a persulfide, analogous to the nomenclature for hydroperoxides.[3] Persulfides are intermediates in the biosynthesis of iron-sulfur proteins[4] and are invoked as precursors to hydrogen sulfide, a biological signaling molecule. Hydropersulfides are thought to mediate many of the antioxidant signaling functions once ascribed purely to hydrogen sulfide via modification of protein cysteine (Cys) residues in a process referred to as persulfidation.[2][5] Hydropersulfides are prototypical reactive sulfur species.

Nomenclature

[edit]

The nomenclature used for organosulfur compounds is often non-systematic. The current literature (in English) has standardized the use of hydropersulfide and persulfide.[2][3] Hydropersulfides may also be described as S-sulfanyl derivatives of their corresponding thiols (i.e. S-sulfanylcysteine for cysteine hydropersulfide). In older literature, persulfides are called hydrodisulfides or hydridodisulfides to further avoid confusion with disulfides with the grouping R-S-S-R, by emphasizing the presence of an H at one end of a disulfide bond. Older literature has also referred to hydropersulfides as "perthiols".[6] Likewise, the formation of protein hydropersulfides from protein thiols in the context of signaling was once referred to as "S-sulfhydration",[6] a term which is now deprecated in favor of "S-persulfidation" or "persulfidation" in the current literature.[2][3]

Chemical properties

[edit]

Hydropersulfides, as with catenated sulfur species in general,[7] are thermodynamically unstable with respect to loss of elemental sulfur:

RSSH → RSH + 1/8 S8

The S-H bond is both more acidic and more fragile than in thiols. Hydropersulfides are on average between 1 and 3 pKa units more acidic than their corresponding thiols, occupying a range of 4.6 to 6.3 for the biologically relevant thiols.[8][9] Thus, persulfides exist predominantly in the ionized form at neutral pH. However, the self-reactivity of hydropersulfides makes reliabie quantification of their pKa values difficult.

The bond dissociation energy of a typical hydropersulfide is 22 kcal/mol weaker than a typical thiol, and the lower pKa of about 6.2 for persulfides compared to 7.5 for thiols. This effect is attributed to the stability of the RSS· radical.[9][10]

Structure and reactivity

[edit]

The structure of trityl hydropersulfide has been determined by X-ray crystallography. The S-S bond length is 204 picometers and the C-S-S-H dihedral angle is 82°. These parameters are unexceptional.[11] (C6H5)3CSSH behaves as a source of sulfur, illustrated by its reaction with triphenylphosphine to give triphenylphosphine sulfide and triphenylmethanethiol:

(C6H5)3CSSH + P(C6H5)3 → (C6H5)3CSH + SP(C6H5)3

Regioselectivity for nucleophilic attack at the two sulfurs of a hydropersulfide depends on the substituents at sulfur.[12] For the reaction of a thiol nucleophile with a hydropersulfide, attack at the terminal sulfur atom results in a net transfer of a sulfhydryl group from the hydropersulfide to the attacking thiol, a reaction known as transpersulfidation. Attack at the inner sulfur atom results in the release of hydrosulfide anion (in equilibrium at neutral pH with hydrogen sulfide) and formation of new disulfide.

R1SSH + R2SH R1SH + R2SSH transpersulfidation

R1SSH + R2SH R1SSR2 + H2S disulfide formation

Both processes are operative in solution. However, transpersulfidation is slightly kinetically favored due to a lower steric barrier. Electron-withdrawing groups on the hydropersulfide stabilize developing negative charge on the inner sulfur atom of the transpersulfidation transition state, further biasing reactivity towards transpersulfidation. The disulfide formation pathway is most competitive when the hydropersulfide is sterically unhindered.

Transpersulfidation from low-molecular weight hydropersulfides onto protein cysteine residues is thought to be the dominant mechanism by which proteins are persulfidated.[3] The instability of hydropersulfides in solution has motivated the design of hydropersulfide donor molecules for biochemical research, which typically operate via transpersulfidation reactivity.[13]

Owing to their increased acidity, hydropersulfides exist as persulfide anions at physiological pH moreso than the corresponding thiols exist as thiolates. The role of the α-effect on this nucleophilicity of persulfides is debated.[13][14] Protonation of hydropersulfides enhances the electrophilicity of the S-S bond.

Under neutral to mildly acidic conditions, where both the electrophilic hydropersulfide and nucleophilic persulfide anion protonation states are present, hydropersulfides reversibly disproportionate to give a complex equilibrium of hydrogen sulfide, persulfides, trisulfides, tetrasulfides and higher-order polysulfides, and elemental sulfur:[15][16]

R1S + R2SSSH R1SSH + R2SS R1SSSR2 + HS

R1SSSR2 + R3SS R3SSSSR2 + R1S → → RxS(S)nSRy

Note that the above equations do not encompass all possible sulfur exchange chemistry and recombination products that could be formed. Trisulfides represent a local thermodynamic minimum for persulfides in dilute solution but are subject to sulfur catenation reactivity. Hydropolysulfides [RS(S)nSH] may also be formed and are expected to possess similar properties to hydropersulfides.[5]

The unique instability of persulfides complicates their detection in biological samples, which is typically performed via alkylation of persulfides with electrophiles such as iodoacetamide derivatives and Michael acceptors such as N-ethylmaleimide.[17][18]

Because of the stability of the perthiyl radical (RSS·), hydropersulfides have been found to be exceptional physiological hydrogen atom transfer reagents comparable to alpha-tocopherol, the canonical lipid membrane-soluble single-electron antioxidant. Hydropersulfides have been found to rapidly inhibit lipid peroxidation chain reactions via conversion of lipid peroxyl radicals to lipid hydroperoxides.[9][19]

Biosynthetic and physiological roles

[edit]

Hydropersulfides may be synthesized directly from hydrogen sulfide via reaction with sulfenic acids, a biologically relevant but short-lived oxoform of cysteine:[20]

RSOH + H2S → RSSH + H2O

Formation of biological hydropersulfide species from hydrogen sulfide and a thiol is a net oxidation process and thus must necessarily occur via some manner of oxidation, even if no obvious oxidizing agent is present.

Cysteine (Cys) hydropersulfide may be generated from cystine via the transsulfuration pathway enzymes cystathionine β-synthase (CBS) and cystathionine γ-lyase (CSE, also referred to as cystathionase).[21] The mitochondrial cysteine aminoacyl-tRNA synthetase CARS2 synthesizes cysteine hydropersulfide from cysteine and allows for co-translational incorporation of hydropersulfides into nascent proteins.[22] The enzyme 3-mercaptopyruvate sulfurtransferase catabolizes 3-mercaptopyruvate to produce an active site Cys hydropersulfide, which may undergo transpersulfidation reactions with thiols or be reduced to release H2S.[23] Sulfide:quinone oxidoreductase (SQOR) oxidizes H2S to form hydropersulfides in the presence of a thiol acceptor such as glutathione.[2] The thiosulfate sulfurtransferase rhodanese interconverts hydropersulfides and thiosulfate.

Cysteine desulfurases also generate active site Cys hydropersulfides, which are used as sulfur sources for the biosynthesis of sulfur-containing cofactors such as 4-thiouridine and thiamine,[24] as well as iron-sulfur cluster assembly in both bacteria[25] and mammalian cells.[26] Mitochondrial iron-sulfur cluster assembly requires transpersulfidation from the Cys desulfurase NFS1 to the iron-sulfur cluster assembly protein ISCU, mediated by the accessory protein frataxin (FXN); loss of effective transpersulfidation from NFS1 via deleterious mutations in FXN results in Friedrich's ataxia.

Persulfides have been invoked as intermediates in the biodegradation of carbon disulfide.[27]

Hydropersulfides are typically thought to be antioxidants due to activation of Nrf2 signaling via persulfidation of Keap1, the inhibitor protein of Nrf2.[2][5] Hydropersulfides also inhibit ferroptosis via depletion of oxidizing radical species.[19][28] Hydropersulfides have been shown to act as physiological protecting groups for protein Cys residues against overoxidation, as they may be sacrificially oxidized to thiosulfonic acids and then cleaved by thioredoxins to regenerate the original protein.[29] However, persulfidation may also act in a pro-oxidant capacity by promoting disulfide formation, which is traditionally considered an oxidative modification in biology.

Persulfides are catabolized in the mitochondria as part of H2S catabolism. Rhodanese may reversibly utilize GSSH as a sulfur source to produce thiosulfate. GSSH is irreversibly degraded by the persulfide dioxygenase ETHE1 to GSH and sulfite, which is further oxidized and excreted.[2] Cysteine hydropersulfide may be directly effluxed from mammalian cells via the cystine/glutamate antiporter SLC7A11.[30]

See also

[edit]

References

[edit]
  1. Park, Chung-Min; Weerasinghe, Laksiri; Day, Jacob J.; Fukuto, Jon M.; Xian, Ming (2015). "Persulfides: Current knowledge and challenges in chemistry and chemical biology". Molecular BioSystems. 11 (7): 1775–1785. doi:10.1039/c5mb00216h. PMC 4470748. PMID 25969163.
  2. 1 2 3 4 5 6 7 Filipovic, Milos R.; Zivanovic, Jasmina; Alvarez, Beatriz; Banerjee, Ruma (2018-02-14). "Chemical Biology of H2S Signaling through Persulfidation". Chemical Reviews. 118 (3): 1253–1337. Bibcode:2018ChRv..118.1253F. doi:10.1021/acs.chemrev.7b00205. ISSN 0009-2665. PMC 6029264. PMID 29112440.
  3. 1 2 3 4 Vignane, Thibaut; Filipovic, Milos R. (2023-07-01). "Emerging Chemical Biology of Protein Persulfidation". Antioxidants & Redox Signaling. 39 (1–3): 19–39. doi:10.1089/ars.2023.0352. ISSN 1523-0864. PMC 10433728. PMID 37288744.
  4. Lill, Roland (2009). "Function and biogenesis of iron–sulphur proteins". Nature. 460 (7257): 831–838. Bibcode:2009Natur.460..831L. doi:10.1038/nature08301. PMID 19675643.
  5. 1 2 3 Nagy, Péter; Dóka, Éva; Domán, Andrea; Paul, Bindu D.; Balla, József; Murphy, Michael P.; Winterbourn, Christine; Radi, Rafael; Snyder, Solomon H.; Ignarro, Louis J.; Sies, Helmut (April 2026). "Multifaceted roles for persulfide species in redox chemical biology". Nature Chemical Biology. 22 (4): 540–555. doi:10.1038/s41589-026-02142-z. ISSN 1552-4469. PMID 41731189.
  6. 1 2 Everett, S. A.; Folkes, L. K.; Wardman, P.; Asmus, K.-D. (1994-01-01). "Free-Radical Repair by a Novel Perthiol: Reversible Hydrogen Transfer and Perthiyl Radical Formation". Free Radical Research. 20 (6): 387–400. doi:10.3109/10715769409145638. ISSN 1071-5762. PMID 8081454.
  7. Williams, Charles R.; Harpp, David N. (1990-08-01). "Sulfur Extrusion Reactions - Scope and Mechanistic Aspects". Sulfur Reports. 10 (2): 103–191. doi:10.1080/01961779008048753. ISSN 0196-1772.
  8. Benchoam, Dayana; Cuevasanta, Ernesto; Roman, Joseph V.; Banerjee, Ruma; Alvarez, Beatriz (May 2024). "Acidity of persulfides and its modulation by the protein environments in sulfide quinone oxidoreductase and thiosulfate sulfurtransferase". The Journal of Biological Chemistry. 300 (5) 107149. doi:10.1016/j.jbc.2024.107149. ISSN 1083-351X. PMC 11039317. PMID 38479599.
  9. 1 2 3 Chauvin, Jean-Philippe R.; Griesser, Markus; Pratt, Derek A. (2017-05-10). "Hydropersulfides: H-Atom Transfer Agents Par Excellence". Journal of the American Chemical Society. 139 (18): 6484–6493. Bibcode:2017JAChS.139.6484C. doi:10.1021/jacs.7b02571. ISSN 0002-7863. PMID 28419803.
  10. Bianco, Christopher L.; Chavez, Tyler A.; Sosa, Victor; Saund, Simran S.; Nguyen, Q. Nhu N.; Tantillo, Dean J.; Ichimura, Andrew S.; Toscano, John P.; Fukuto, Jon M. (December 2016). "The chemical biology of the persulfide (RSSH)/perthiyl (RSS·) redox couple and possible role in biological redox signaling". Free Radical Biology & Medicine. 101: 20–31. doi:10.1016/j.freeradbiomed.2016.09.020. ISSN 1873-4596. PMC 5154930. PMID 27677567.
  11. Bailey, T. Spencer; Zakharov, Lev N.; Pluth, Michael D. (2014). "Understanding Hydrogen Sulfide Storage: Probing Conditions for Sulfide Release from Hydrodisulfides". Journal of the American Chemical Society. 136 (30): 10573–10576. Bibcode:2014JAChS.13610573B. doi:10.1021/ja505371z. PMC 4120993. PMID 25010540.
  12. Fosnacht, Kaylin G.; Sharma, Jyoti; Champagne, Pier Alexandre; Pluth, Michael D. (2024-07-10). "Transpersulfidation or H2S Release? Understanding the Landscape of Persulfide Chemical Biology". Journal of the American Chemical Society. 146 (27): 18689–18698. Bibcode:2024JAChS.14618689F. doi:10.1021/jacs.4c05874. ISSN 0002-7863. PMID 38935871.
  13. 1 2 Liu, Daniel; Lamar, Jordan; Thampoe, Andrew; Khodade, Vinayak S.; Toscano, John P. (2026-07-01). "Hydropersulfide Donors: Mechanistic and Kinetic Insights With Biological and Potential Therapeutic Implications". Journal of Physical Organic Chemistry. 39 (7) e70087. doi:10.1002/poc.70087. ISSN 1099-1395.
  14. Switzer, Christopher H. (2023-09-23). "How super is supersulfide?: Reconsidering persulfide reactivity in cellular biology". Redox Biology. 67 102899. doi:10.1016/j.redox.2023.102899. ISSN 2213-2317. PMC 10522965. PMID 37748320.
  15. Bailey, T. Spencer; Pluth, Michael D. (December 2015). "Reactions of isolated persulfides provide insights into the interplay between H2S and persulfide reactivity". Free Radical Biology & Medicine. 89: 662–667. doi:10.1016/j.freeradbiomed.2015.08.017. ISSN 1873-4596. PMC 4684792. PMID 26454077.
  16. Saund, Simran S.; Sosa, Victor; Henriquez, Stephanie; Nguyen, Q. Nhu N.; Bianco, Christopher L.; Soeda, Shuhei; Millikin, Robert; White, Corey; Le, Henry; Ono, Katsuhiko; Tantillo, Dean J.; Kumagai, Yoshito; Akaike, Takaaki; Lin, Joseph; Fukuto, Jon M. (2015-12-15). "The chemical biology of hydropersulfides (RSSH): Chemical stability, reactivity and redox roles". Archives of Biochemistry and Biophysics. 588: 15–24. doi:10.1016/j.abb.2015.10.016. ISSN 1096-0384. PMC 4833115. PMID 26519887.
  17. Bogdándi, Virág; Ida, Tomoaki; Sutton, Thomas R; Bianco, Christopher; Ditrói, Tamás; Koster, Grielof; Henthorn, Hillary A; Minnion, Magda; Toscano, John P; van der Vliet, Albert; Pluth, Michael D; Feelisch, Martin; Fukuto, Jon M; Akaike, Takaaki; Nagy, Péter (2019). "Speciation of reactive sulfur species and their reactions with alkylating agents: do we have any clue about what is present inside the cell?". British Journal of Pharmacology. 176 (4): 646–670. doi:10.1111/bph.14394. ISSN 1476-5381. PMC 6346080. PMID 29909607.
  18. Schilling, Danny; Barayeu, Uladzimir; Steimbach, Raphael R.; Talwar, Deepti; Miller, Aubry K.; Dick, Tobias P. (2022). "Commonly Used Alkylating Agents Limit Persulfide Detection by Converting Protein Persulfides into Thioethers". Angewandte Chemie International Edition. 61 (30) e202203684. Bibcode:2022ACIE...61E3684S. doi:10.1002/anie.202203684. ISSN 1521-3773. PMC 9401046. PMID 35506673.
  19. 1 2 Wu, Zijun; Khodade, Vinayak S.; Chauvin, Jean-Philippe R.; Rodriguez, Deborah; Toscano, John P.; Pratt, Derek A. (2022-08-31). "Hydropersulfides Inhibit Lipid Peroxidation and Protect Cells from Ferroptosis". Journal of the American Chemical Society. 144 (34): 15825–15837. Bibcode:2022JAChS.14415825W. doi:10.1021/jacs.2c06804. ISSN 0002-7863. PMID 35977425.
  20. Cuevasanta, Ernesto; Lange, Mike; Bonanata, Jenner; Coitiño, E. Laura; Ferrer-Sueta, Gerardo; Filipovic, Milos R.; Alvarez, Beatriz (2015-11-06). "Reaction of Hydrogen Sulfide with Disulfide and Sulfenic Acid to Form the Strongly Nucleophilic Persulfide". The Journal of Biological Chemistry. 290 (45): 26866–26880. Bibcode:2015JBiCh.29026866C. doi:10.1074/jbc.M115.672816. ISSN 1083-351X. PMC 4646399. PMID 26269587.
  21. Ida, Tomoaki; Sawa, Tomohiro; Ihara, Hideshi; Tsuchiya, Yukihiro; Watanabe, Yasuo; Kumagai, Yoshito; Suematsu, Makoto; Motohashi, Hozumi; Fujii, Shigemoto; Matsunaga, Tetsuro; Yamamoto, Masayuki; Ono, Katsuhiko; Devarie-Baez, Nelmi O.; Xian, Ming; Fukuto, Jon M. (2014-05-27). "Reactive cysteine persulfides and S-polythiolation regulate oxidative stress and redox signaling". Proceedings of the National Academy of Sciences. 111 (21): 7606–7611. Bibcode:2014PNAS..111.7606I. doi:10.1073/pnas.1321232111. PMC 4040604. PMID 24733942.
  22. Akaike, Takaaki; Ida, Tomoaki; Wei, Fan-Yan; Nishida, Motohiro; Kumagai, Yoshito; Alam, Md Morshedul; Ihara, Hideshi; Sawa, Tomohiro; Matsunaga, Tetsuro; Kasamatsu, Shingo; Nishimura, Akiyuki; Morita, Masanobu; Tomizawa, Kazuhito; Nishimura, Akira; Watanabe, Satoshi (2017-10-27). "Cysteinyl-tRNA synthetase governs cysteine polysulfidation and mitochondrial bioenergetics". Nature Communications. 8 (1): 1177. Bibcode:2017NatCo...8.1177A. doi:10.1038/s41467-017-01311-y. ISSN 2041-1723. PMC 5660078. PMID 29079736.
  23. Pedre, Brandán; Talwar, Deepti; Barayeu, Uladzimir; Schilling, Danny; Luzarowski, Marcin; Sokolowski, Mikolaj; Glatt, Sebastian; Dick, Tobias P. (April 2023). "3-Mercaptopyruvate sulfur transferase is a protein persulfidase". Nature Chemical Biology. 19 (4): 507–517. doi:10.1038/s41589-022-01244-8. ISSN 1552-4469. PMC 10060159. PMID 36732619.
  24. Mueller, Eugene G. (April 2006). "Trafficking in persulfides: delivering sulfur in biosynthetic pathways". Nature Chemical Biology. 2 (4): 185–194. doi:10.1038/nchembio779. ISSN 1552-4469. PMID 16547481.
  25. Gogar, Rajleen K.; Chhikara, Nidhi; Vo, Minh; Gilbert, Nathaniel C.; Dunkle, Jack A.; Frantom, Patrick A. (2024-09-01). "The structure of the SufS–SufE complex reveals interactions driving protected persulfide transfer in iron-sulfur cluster biogenesis". Journal of Biological Chemistry. 300 (9) 107641. Bibcode:2024JBiCh.300j7641G. doi:10.1016/j.jbc.2024.107641. ISSN 0021-9258. PMC 11408855. PMID 39122000.
  26. Parent, Aubérie; Elduque, Xavier; Cornu, David; Belot, Laura; Le Caer, Jean-Pierre; Grandas, Anna; Toledano, Michel B.; D'Autréaux, Benoit (2015-01-19). "Mammalian frataxin directly enhances sulfur transfer of NFS1 persulfide to both ISCU and free thiols". Nature Communications. 6 (1): 5686. Bibcode:2015NatCo...6.5686P. doi:10.1038/ncomms6686. ISSN 2041-1723. PMID 25597503.
  27. Catignani, George L., Robert A. Neal (1975). "Evidence for the formation of a protein bound hydrodisulfide resulting from the microsomal mixed function oxidase catalyzed desulfuration of carbon disulfide". Biochemical and Biophysical Research Communications. 65 (2): 629–636. Bibcode:1975BBRC...65..629C. doi:10.1016/S0006-291X(75)80193-8. PMID 238535.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  28. Barayeu, Uladzimir; Schilling, Danny; Eid, Mohammad; Xavier da Silva, Thamara Nishida; Schlicker, Lisa; Mitreska, Nikolina; Zapp, Christopher; Gräter, Frauke; Miller, Aubry K.; Kappl, Reinhard; Schulze, Almut; Friedmann Angeli, José Pedro; Dick, Tobias P. (January 2023). "Hydropersulfides inhibit lipid peroxidation and ferroptosis by scavenging radicals". Nature Chemical Biology. 19 (1): 28–37. doi:10.1038/s41589-022-01145-w. ISSN 1552-4469. PMC 7613997. PMID 36109647.
  29. Dóka, É.; Ida, T.; Dagnell, M.; Abiko, Y.; Luong, N. C.; Balog, N.; Takata, T.; Espinosa, B.; Nishimura, A.; Cheng, Q.; Funato, Y.; Miki, H.; Fukuto, J. M.; Prigge, J. R.; Schmidt, E. E. (January 2020). "Control of protein function through oxidation and reduction of persulfidated states". Science Advances. 6 (1) eaax8358. Bibcode:2020SciA....6.8358D. doi:10.1126/sciadv.aax8358. PMC 6938701. PMID 31911946.
  30. Akiyama, Masahiro; Unoki, Takamitsu; Aoki, Hanako; Nishimura, Akiyuki; Shinkai, Yasuhiro; Warabi, Eiji; Nishiyama, Kazuhiro; Furumoto, Yuka; Anzai, Naohiko; Akaike, Takaaki; Nishida, Motohiro; Kumagai, Yoshito (November 2022). "Cystine-dependent antiporters buffer against excess intracellular reactive sulfur species-induced stress". Redox Biology. 57 102514. doi:10.1016/j.redox.2022.102514. ISSN 2213-2317. PMC 9594640. PMID 36279630.