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Transient Catalytic Voltammetry of Sulfite Oxidase Reveals Rate Limiting Conformational Changes

  • Sulfite oxidases are metalloenzymes that oxidize sulfite to sulfate at a molybdenum active site. In vertebrate sulfite oxidases, the electrons generated at the Mo center are transferred to an external electron acceptor via a heme domain, which can adopt two conformations: a “closed” conformation, suitable for internal electron transfer, and an “open” conformation suitable for intermolecular electron transfer. This conformational change is an integral part of the catalytic cycle. Sulfite oxidases have been wired to electrode surfaces, but their immobilization leads to a significant decrease in their catalytic activity, raising the question of the occurrence of the conformational change when the enzyme is on an electrode. We recorded and quantitatively modeled for the first time the transient response of the catalytic cycle of human sulfite oxidase immobilized on an electrode. We show that conformational changes still occur on the electrode, but at a lower rate than in solution, which is the reason for the decrease in activity ofSulfite oxidases are metalloenzymes that oxidize sulfite to sulfate at a molybdenum active site. In vertebrate sulfite oxidases, the electrons generated at the Mo center are transferred to an external electron acceptor via a heme domain, which can adopt two conformations: a “closed” conformation, suitable for internal electron transfer, and an “open” conformation suitable for intermolecular electron transfer. This conformational change is an integral part of the catalytic cycle. Sulfite oxidases have been wired to electrode surfaces, but their immobilization leads to a significant decrease in their catalytic activity, raising the question of the occurrence of the conformational change when the enzyme is on an electrode. We recorded and quantitatively modeled for the first time the transient response of the catalytic cycle of human sulfite oxidase immobilized on an electrode. We show that conformational changes still occur on the electrode, but at a lower rate than in solution, which is the reason for the decrease in activity of sulfite oxidases upon immobilization.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Ting Zeng, Silke LeimkühlerORCiDGND, Ulla WollenbergerORCiDGND, Vincent FourmondORCiD
DOI:https://doi.org/10.1021/jacs.7b05480
ISSN:0002-7863
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/28727916
Titel des übergeordneten Werks (Englisch):Journal of the American Chemical Society
Verlag:American Chemical Society
Verlagsort:Washington
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Jahr der Erstveröffentlichung:2017
Erscheinungsjahr:2017
Datum der Freischaltung:20.04.2020
Band:139
Seitenanzahl:9
Erste Seite:11559
Letzte Seite:11567
Fördernde Institution:CNRS; Agence Nationale de la Recherche [ANR-12-BS08-0014, Government program [ANR-11-IDEX-0001-02]; Deutsche Forschungsgemeinschaft (Unicat Cluster of Excellence) [EXC 314]
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
Peer Review:Referiert
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