Mechanistic insight into the catalytic inhibition by nitroxides of tyrosine oxidation and nitration
Nitroxide antioxidants (RNO•) protect from injuries associated with oxidative stress. Tyrosine residues in proteins are major targets for oxidizing species giving rise to irreversible cross-linking and protein nitration, but the mechanisms underlying the protective activity of RNO• on these processe...
Saved in:
Published in | Biochimica et biophysica acta. General subjects Vol. 1863; no. 11; p. 129403 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.11.2019
|
Subjects | |
Online Access | Get full text |
ISSN | 0304-4165 1872-8006 1872-8006 |
DOI | 10.1016/j.bbagen.2019.07.012 |
Cover
Summary: | Nitroxide antioxidants (RNO•) protect from injuries associated with oxidative stress. Tyrosine residues in proteins are major targets for oxidizing species giving rise to irreversible cross-linking and protein nitration, but the mechanisms underlying the protective activity of RNO• on these processes are not sufficiently clear.
Tyrosine oxidation by the oxoammonium cation (RN+=O) was studied by following the kinetics of RNO• formation using EPR spectroscopy. Tyrosine oxidation and nitration were investigated using the peroxidase/H2O2 system without and with nitrite. The inhibitory effect of RNO• on these processes was studied by following the kinetics of the evolved O2 and accumulation of tyrosine oxidation and nitration products.
Tyrosine ion is readily oxidized by RN+=O, and the equilibrium constant of this reaction depends on RNO• structure and reduction potential. RNO• catalytically inhibits tyrosine oxidation and nitration since it scavenges both tyrosyl and •NO2 radicals while recycling through RN+=O reduction by H2O2, tyrosine and nitrite. The inhibitory effect of nitroxide on tyrosine oxidation and nitration increases as its reduction potential decreases where the 6-membered ring nitroxides are better catalysts than the 5-membered ones.
Nitroxides catalytically inhibit tyrosine oxidation and nitration. The proposed reaction mechanism adequately fits the results explaining the dependence of the nitroxide inhibitory effect on its reduction potential and on the concentrations of the reducing species present in the system.
Nitroxides protect against both oxidative and nitrative damage. The proposed reaction mechanism further emphasizes the role of the reducing environment to the efficacy of these catalysts.
[Display omitted]
•Nitroxides catalytically inhibit tyrosine oxidation mediated by peroxidase/H2O2.•Nitroxide catalysts inhibit tyrosine nitration mediated by peroxidase/H2O2/nitrite.•The inhibitory effect increases as nitroxide reduction potential decreases.•The 6-membered ring nitroxides are better catalyst than the 5-memnbered ones.•The proposed mechanism implies a role of reducing agents on nitroxide efficacy. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0304-4165 1872-8006 1872-8006 |
DOI: | 10.1016/j.bbagen.2019.07.012 |