Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/55830
Título: Probing the role of the hinge segment of cytochrome P450 oxidoreductase in the interaction with cytochrome P450
Autor: Campelo, Diana
Esteves, Francisco
Palma, Bernardo Brito
Gomes, Bruno Costa
Rueff, José
Lautier, Thomas
Urban, Philippe
Truan, Gilles
Kranendonk, Michel
Palavras-chave: Cytochrome b5 (CYB5)
Electron-transfer (ET)
Microsomal cytochrome p450 (CYP)
NADPH-cytochrome P450 reductase (CPR)
Protein dynamics
Protein-protein interaction
Molecular Biology
Computer Science Applications
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry
Data: 1-Dez-2018
Resumo: NADPH-cytochrome P450 reductase (CPR) is the unique redox partner of microsomal cytochrome P450s (CYPs). CPR exists in a conformational equilibrium between open and closed conformations throughout its electron transfer (ET) function. Previously, we have shown that electrostatic and flexibility properties of the hinge segment of CPR are critical for ET. Three mutants of human CPR were studied (S243P, I245P and R246A) and combined with representative human drug-metabolizing CYPs (isoforms 1A2, 2A6 and 3A4). To probe the effect of these hinge mutations different experimental approaches were employed: CYP bioactivation capacity of pre-carcinogens, enzyme kinetic analysis, and effect of the ionic strength and cytochrome b5 (CYB5) on CYP activity. The hinge mutations influenced the bioactivation of pre-carcinogens, which seemed CYP isoform and substrate dependent. The deviations of Michaelis-Menten kinetic parameters uncovered tend to confirm this discrepancy, which was confirmed by CYP and hinge mutant specific salt/activity profiles. CPR/CYB5 competition experiments indicated a less important role of affinity in CPR/CYP interaction. Overall, our data suggest that the highly flexible hinge of CPR is responsible for the existence of a conformational aggregate of different open CPR conformers enabling ET-interaction with structural varied redox partners.
Peer review: yes
URI: http://www.scopus.com/inward/record.url?scp=85058293841&partnerID=8YFLogxK
DOI: https://doi.org/10.3390/ijms19123914
ISSN: 1661-6596
Aparece nas colecções:NMS-FCM: ToxOmics - Artigos em revista internacional com arbitragem científica

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