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001-es BibID:BIBFORM062918
Első szerző:Dóka Éva (vegyész)
Cím:A novel persulfide detection method reveals protein persulfide- and polysulfide-reducing functions of thioredoxin and glutathione systems / Éva Dóka, Irina Pader, Adrienn Bíró, Katarina Johansson, Qing Cheng, Krisztina Ballagó, Justin R. Prigge, Daniel Pastor-Flores, Tobias P. Dick, Edward E. Schmidt, Elias S. J. Arnér, Péter Nagy
Dátum:2016
ISSN:2375-2548
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Science Advances. - 2 : 1 (2016), p. e1500968. -
További szerzők:Pader, Irina Bíró Adrienn Johansson, Katarina Cheng, Qing Ballagó Krisztina Prigge, Justin R. Pastor-Flores, Daniel Dick, Tobias P. Schmidt, Edward E. Arner, Elias S. J. Nagy Péter
Internet cím:DOI
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001-es BibID:BIBFORM062162
Első szerző:Vasas Anita (környezetkutató)
Cím:Kinetic and thermodynamic studies on the disulfide-bond reducing potential of hydrogen sulfide / Anita Vasas, Éva Dóka, István Fábián, Péter Nagy
Dátum:2015
ISSN:1089-8603
Megjegyzések:The significance of persulfide species in hydrogen sulfide biology is increasingly recognized. However,the molecular mechanisms of their formation remain largely elusive. The obvious pathway of the reduction of biologically abundant disulfide moieties by sulfide was challenged on both thermodynamicand kinetic grounds. Using DTNB (5,5·-dithiobis-(2-nitrobenzoic acid), also known as Ellman's reagent)as a model disulfide we conducted a comprehensive kinetic study for its reaction with sulfide. The bimolecular reaction is relatively fast with a second-order rate constant of 889 ? 12 M?1s?1 at pH = 7.4. pHdependence of the rate law revealed that the reaction proceeds via the bisulfide anion species with aninitial nucleophilic thiol-disulfide exchange reaction to give 5-thio-2-nitrobenzoic acid (TNB) and TNBpersulfide with a pH independent second-order rate constant of 1090 ? 12 M?1s?1. However, kinetic studiesand stoichiometric analyses in a wide range of reactant ratios together with kinetic simulations revealed that it is a multistep process that proceeds via kinetically driven, practically irreversible reactionsalong the disulfide ? persulfide ? inorganic polysulfides axis. The kinetic model postulated here, whichis fully consistent with the experimental data, suggests that the TNB-persulfide is further reduced bysulfide with a second-order rate constant in the range of 5 ? 103 ? 5 ? 104 M?1s?1 at pH 7.4 and eventually yields inorganic polysulfides and TNB. The reactions of cystine and GSSG with sulfide were foundto be significantly slower and to occur via more complicated reaction schemes. 1H NMR studies suggestthat these reactions also generate Cys-persulfide and inorganic polysulfide species, but in contrast withDTNB, in consecutive equilibrium processes that are sensitive to changes in the reactant and productratios. Collectively, our results demonstrate that the reaction of disulfides with sulfide is a highly systemspecific process from both thermodynamic and kinetic aspects, which together with the considerablesteady-state concentrations of the reactants in biological systems signifies physiological relevance.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
Hydrogen sulfide
Disulfide reduction
Persulfide
Kinetics and mechanisms
Speciation
Megjelenés:Nitric Oxide-Biology And Chemistry. - 46 (2015), p. 93-101. -
További szerzők:Dóka Éva (1988-) (vegyész) Fábián István (1956-) (vegyész) Nagy Péter
Internet cím:Szerző által megadott URL
DOI
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