Adrenodoxin allosterically alters human cytochrome P450 11B enzymes to accelerate substrate binding and decelerate release.


Journal

RSC chemical biology
ISSN: 2633-0679
Titre abrégé: RSC Chem Biol
Pays: England
ID NLM: 101768727

Informations de publication

Date de publication:
02 Aug 2024
Historique:
received: 15 01 2024
accepted: 22 07 2024
medline: 12 8 2024
pubmed: 12 8 2024
entrez: 12 8 2024
Statut: aheadofprint

Résumé

Two human mitochondrial membrane CYP11B enzymes play a pivotal role in steroidogenesis. CYP11B1 generates the major glucocorticoid cortisol, while CYP11B2 catalysis yields the primary mineralocorticoid aldosterone. Catalysis by both requires electron delivery by a soluble iron-sulfur adrenodoxin redox partner. However recent studies have shown that adrenodoxin/CYP11B interaction alone allosterically increases substrate and inhibitor affinity as exhibited by decreased dissociation constant (

Identifiants

pubmed: 39129792
doi: 10.1039/d4cb00015c
pii: d4cb00015c
pmc: PMC11310744
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

The authors declare that they have no conflicts of interest with the contents of this article.

Auteurs

Cara L Loomis (CL)

Department of Biological Chemistry, University of Michigan Ann Arbor MI 48109 USA scottee@umich.edu.

Sang-Choul Im (SC)

Division of Metabolism, Endocrinology, & Diabetes, Department of Internal Medicine, University of Michigan Ann Arbor MI USA.
Ann Arbor Veterans Affairs Medical Center Ann Arbor MI USA.

Emily E Scott (EE)

Department of Biological Chemistry, University of Michigan Ann Arbor MI 48109 USA scottee@umich.edu.
Department of Medicinal Chemistry, University of Michigan Ann Arbor MI 48109 USA.
Department of Pharmacology, University of Michigan Ann Arbor MI 48109 USA.

Classifications MeSH