Theoretical insights into the mechanism of redox switch in heat shock protein Hsp33

Verfasser / Beitragende:
[Mironel Enescu, Rima Kassim, Christophe Ramseyer, Bruno Cardey]
Ort, Verlag, Jahr:
2015
Enthalten in:
JBIC Journal of Biological Inorganic Chemistry, 20/3(2015-04-01), 555-562
Format:
Artikel (online)
ID: 605507260
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024 7 0 |a 10.1007/s00775-015-1240-z  |2 doi 
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245 0 0 |a Theoretical insights into the mechanism of redox switch in heat shock protein Hsp33  |h [Elektronische Daten]  |c [Mironel Enescu, Rima Kassim, Christophe Ramseyer, Bruno Cardey] 
520 3 |a Heat shock protein 33 (Hsp33) is activated in the presence of H2O2 by a very interesting redox switch based on a tetra-coordinated zinc-cysteine complex present in the fully reduced and inactive protein form. The oxidation of this zinc center by H2O2 induces formation of two S-S bridges and the zinc release followed by the protein unfolding. We report here a theoretical study of the step-by-step sequence of the overall process starting with the oxidation of the first cysteine residue and ending with the zinc release. Each reaction step is characterized by its Gibbs free energy barrier (∆G ‡). It is predicted that the first reaction step consists in the oxidation of Cys263 by H2O2 which is by far the most reactive cysteine (∆G ‡=15.4kcalmol−1). The next two reaction steps are the formation of the first S-S bridge between Cys263 and Cys266 (∆G ‡=13.6kcalmol−1) and the oxidation of Cys231 by H2O2 (∆G ‡=20.4kcalmol−1). It is then shown that the formation of the second S-S bridge (Cys231-Cys233) before the zinc release is most unlikely (∆G ‡=34.8kcalmol−1). Instead, the release of zinc just after the oxidation of the third cysteine (Cys231) is shown to be thermodynamically (dissociation Gibbs free energy ∆G d=6.0kcalmol−1) and kinetically (reaction rate constant k d≈106s−1) favored. This result is in good agreement with the experimental data on the oxidation mechanism of Hsp33 zinc center available to date. 
540 |a SBIC, 2015 
690 7 |a Hsp33  |2 nationallicence 
690 7 |a Redox switch  |2 nationallicence 
690 7 |a Hydrogen peroxide  |2 nationallicence 
690 7 |a Ab initio  |2 nationallicence 
690 7 |a Energy barrier  |2 nationallicence 
700 1 |a Enescu  |D Mironel  |u Laboratoire Chrono Environnement UMR CNRS 6249, University of Franche-Comté, 16 route de Gray, 25030, Besançon Cedex, France  |4 aut 
700 1 |a Kassim  |D Rima  |u Centre de Recherche Universitaire de Djibouti (CRUD), University of Djibouti, Avenue Georges Clemenceau, Djibouti, Djibouti  |4 aut 
700 1 |a Ramseyer  |D Christophe  |u Laboratoire Chrono Environnement UMR CNRS 6249, University of Franche-Comté, 16 route de Gray, 25030, Besançon Cedex, France  |4 aut 
700 1 |a Cardey  |D Bruno  |u Laboratoire Chrono Environnement UMR CNRS 6249, University of Franche-Comté, 16 route de Gray, 25030, Besançon Cedex, France  |4 aut 
773 0 |t JBIC Journal of Biological Inorganic Chemistry  |d Springer Berlin Heidelberg  |g 20/3(2015-04-01), 555-562  |x 0949-8257  |q 20:3<555  |1 2015  |2 20  |o 775 
856 4 0 |u https://doi.org/10.1007/s00775-015-1240-z  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00775-015-1240-z  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Enescu  |D Mironel  |u Laboratoire Chrono Environnement UMR CNRS 6249, University of Franche-Comté, 16 route de Gray, 25030, Besançon Cedex, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kassim  |D Rima  |u Centre de Recherche Universitaire de Djibouti (CRUD), University of Djibouti, Avenue Georges Clemenceau, Djibouti, Djibouti  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ramseyer  |D Christophe  |u Laboratoire Chrono Environnement UMR CNRS 6249, University of Franche-Comté, 16 route de Gray, 25030, Besançon Cedex, France  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Cardey  |D Bruno  |u Laboratoire Chrono Environnement UMR CNRS 6249, University of Franche-Comté, 16 route de Gray, 25030, Besançon Cedex, France  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t JBIC Journal of Biological Inorganic Chemistry  |d Springer Berlin Heidelberg  |g 20/3(2015-04-01), 555-562  |x 0949-8257  |q 20:3<555  |1 2015  |2 20  |o 775