4.8 Review

Biochemistry of Peroxynitrite and Protein Tyrosine Nitration

Journal

CHEMICAL REVIEWS
Volume 118, Issue 3, Pages 462-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrev.7b00568

Keywords

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Funding

  1. Universidad de la Republica (CSIC)
  2. Universidad de la Republica (Espacio Interdisciplinario, UdelaR)
  3. Agencia Nacional de Investigation e Innovation [FCE_2014_104233]
  4. Programa de Desarrollo de Ciencias Basicas (PEDECIBA)
  5. Centro de Biologia Estructural del Mercosur (CeBEM)
  6. Centro Argentino Brasileno de Biotecnologia (CABBIO)
  7. Ridaline through Fundacion Manuel Perez (Facultad de Medicina, Universidad de la Republica)
  8. Universidad de la Republica (CAP_Uruguay)

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Peroxynitrite is a short-lived and reactive biological oxidant formed from the diffusion-controlled reaction of the free radicals superoxide (O-2(center dot-)) and nitric oxide ((NO)-N-center dot). In this review, we first analyze the biochemical evidence for the formation of peroxynitrite in vivo and the reactions that lead to it. Then, we describe the principal reactions that peroxynitrite undergoes with biological targets and provide kinetic and mechanistic details.. In these reactions, peroxynitrite has roles as (1) peroxide, (2) Lewis base, and (3) free radical generator. Physiological levels of CO2 can change the outcome of peroxynitrite reactions. The second part of the review assesses the formation of protein 3-nitrotyrosine ((center dot)NO(2)Tyr) by peroxynitrite-dependent and-independent mechanisms, as one of the hallmarks of the actions of (NO)-N-center dot-derived oxidants in biological systems. Moreover, tyrosine nitration impacts protein structure and function, tyrosine kinase signal transduction cascades and protein turnover. Overall, the review is aimed to provide an integrated biochemical view on the formation and reactions of peroxynitrite under biologically relevant conditions and the impact of this stealthy oxidant and one of its major footprints, protein NO(2)Tyr, in the disruption of cellular homeostasis.

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