Structure and mechanisms of ROS generation by NADPH oxidases.
Journal
Current opinion in structural biology
ISSN: 1879-033X
Titre abrégé: Curr Opin Struct Biol
Pays: England
ID NLM: 9107784
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
10
01
2019
revised:
14
02
2019
accepted:
04
03
2019
pubmed:
6
5
2019
medline:
4
8
2020
entrez:
4
5
2019
Statut:
ppublish
Résumé
NADPH oxidases (NOXs) are integral membrane enzymes that produce reactive oxygen species. Humans have seven NOX enzymes that feature a very similar catalytic core but distinct regulatory mechanisms. The recent structural elucidation of the NOX catalytic domains has been a step forward in the field. NADPH, FAD, and two hemes form a linear array of redox cofactors that transfer electrons across to the two sides of the membrane. Oxygen is reduced through an unusual outer sphere mechanism that does not involve any covalent intermediate with the heme iron. Several recent studies have expanded the roles of NOXs in cell signaling, innate immune response, and cell proliferation including oncogenic transformation. This work reinforces NOX-generated ROS as powerful signaling molecules. A challenging question is to understand the specific mechanisms of enzyme regulation and to harness the growing insight on NOXs' structure and biochemistry to generate more powerful small-molecule modulators of NOX activities.
Identifiants
pubmed: 31051297
pii: S0959-440X(18)30180-5
doi: 10.1016/j.sbi.2019.03.001
pii:
doi:
Substances chimiques
Reactive Oxygen Species
0
NADPH Oxidases
EC 1.6.3.-
Oxygen
S88TT14065
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
91-97Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.