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PMID: 10692434 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Dityrosine formation outcompetes tyrosine nitration at low steady-state concentrations of peroxynitrite. Implications for tyrosine modification by nitric oxide/superoxide in vivo.

The Journal of biological chemistry ·Vol. 275 ·No. 9 ·2000-03-03 ·Pages 6346-52

Pfeiffer S, Schmidt K, Mayer B

Abstract

Formation of peroxynitrite from NO and O-(*2) is considered an important trigger for cellular tyrosine nitration under pathophysiological conditions. However, this view has been questioned by a recent report indicating that NO and O-(*2) generated simultaneously from (Z)-1-(N-[3-aminopropyl]-N-[4-(3-aminopropylammonio)butyl]-amino) diazen-1-ium-1,2-diolate] (SPER/NO) and hypoxanthine/xanthine oxidase, respectively, exhibit much lower nitrating efficiency than authentic peroxynitrite (Pfeiffer, S. and Mayer, B. (1998) J. Biol. Chem. 273, 27280-27285). The present study extends those earlier findings to several alternative NO/O-(*2)-generating systems and provides evidence that the apparent lack of tyrosine nitration by NO/O-(*2) is due to a pronounced decrease of nitration efficiency at low steady-state concentrations of authentic peroxynitrite. The decrease in the yields of 3-nitrotyrosine was accompanied by an increase in the recovery of dityrosine, showing that dimerization of tyrosine radicals outcompetes the nitration reaction at low peroxynitrite concentrations. The observed inverse dependence on peroxynitrite concentration of dityrosine formation and tyrosine nitration is predicted by a kinetic model assuming that radical formation by peroxynitrous acid homolysis results in the generation of tyrosyl radicals that either dimerize to yield dityrosine or combine with (*)NO(2) radical to form 3-nitrotyrosine. The present results demonstrate that very high fluxes (>2 microM/s) of NO/O-(*2) are required to render peroxynitrite an efficient trigger of tyrosine nitration and that dityrosine is a major product of tyrosine modification caused by low steady-state concentrations of peroxynitrite.

MeSH Terms
Dimerization Flavin Mononucleotide/pharmacology Free Radicals/chemistry Hydrazines/chemistry Hypoxanthine/metabolism Kinetics Nitrates/chemistry Nitric Oxide/chemistry Nitrogen Oxides Spermine/analogs & derivatives,chemistry Tyrosine/analogs & derivatives,chemistry Xanthine Oxidase/metabolism
Chemicals
Free Radicals Hydrazines Nitrates Nitrogen Oxides spermine nitric oxide complex peroxynitric acid Spermine Hypoxanthine Nitric Oxide 3-nitrotyrosine Tyrosine Flavin Mononucleotide 1,1-diethyl-2-hydroxy-2-nitrosohydrazine dityrosine Xanthine Oxidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pfeiffer S
Institut für Pharmakologie und Toxikologie, Karl-Franzens-Universität Graz, Universitätsplatz 2, A-8010 Graz, Austria. [email protected]
Schmidt K
Mayer B
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2000-03-03
Pages
6346-52
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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