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Mitigation of NADPH Oxidase 2 Activity as a Strategy to Inhibit Peroxynitrite Formation

Authors :
Lynn VerPlank
Balaraman Kalyanaraman
Jacek Zielonka
Olivier Ouari
Radosław Podsiadły
Monika Zielonka
J. David Lambeth
Gang Cheng
Mehmet Menaf Ayhan
Adam Sikora
Micael Hardy
Medical College of Wisconsin
Broad Institute of MIT and Harvard (BROAD INSTITUTE)
Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston]
Institut de Chimie Radicalaire (ICR)
Aix Marseille Université (AMU)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Institute of Polymer and Dye Technology [Łódź University of Technology]
Łódź University of Technology
Institute of Applied Radiation Chemistry, Technical University of Lodz
Department of Pathology & Laboratory Medicine
Emory University [Atlanta, GA]
Source :
Journal of Biological Chemistry, Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2016, 291, pp.7029-7044. ⟨10.1074/jbc.M115.702787⟩, Journal of Biological Chemistry, 2016, 291, pp.7029-7044. ⟨10.1074/jbc.M115.702787⟩
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

Using high throughput screening-compatible assays for superoxide and hydrogen peroxide, we identified potential inhibitors of the NADPH oxidase (Nox2) isoform from a small library of bioactive compounds. By using multiple probes (hydroethidine, hydropropidine, Amplex Red, and coumarin boronate) with well defined redox chemistry that form highly diagnostic marker products upon reaction with superoxide (O2 (̇̄)), hydrogen peroxide (H2O2), and peroxynitrite (ONOO(-)), the number of false positives was greatly decreased. Selected hits for Nox2 were further screened for their ability to inhibit ONOO(-)formation in activated macrophages. A new diagnostic marker product for ONOO(-)is reported. We conclude that the newly developed high throughput screening/reactive oxygen species assays could also be used to identify potential inhibitors of ONOO(-)formed from Nox2-derived O2 (̇̄)and nitric oxide synthase-derived nitric oxide.

Details

ISSN :
00219258 and 1083351X
Volume :
291
Database :
OpenAIRE
Journal :
Journal of Biological Chemistry
Accession number :
edsair.doi.dedup.....6eaeb47228111c2e44875990bb9d14c3