Photochemistry of tyrosine dimer: when an oxidative lesion of proteins is able to photoinduce further damage.


Journal

Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
ISSN: 1474-9092
Titre abrégé: Photochem Photobiol Sci
Pays: England
ID NLM: 101124451

Informations de publication

Date de publication:
10 Jul 2019
Historique:
pubmed: 10 5 2019
medline: 18 7 2019
entrez: 10 5 2019
Statut: ppublish

Résumé

The tyrosine dimer (Tyr2), a covalent bond between two tyrosines (Tyr), is one of the most important modifications of the oxidative damage of proteins. This compound is increasingly used as a marker of aging, stress and pathogenesis. At physiological pH, Tyr2 is able to absorb radiation at wavelengths significantly present in the solar radiation and artificial sources of light. As a result, when Tyr2 is formed in vivo, a new chromophore appears in the proteins. Despite the biomedical importance of Tyr2, the information of its photochemical properties is limited due to the drawbacks of its synthesis. Therefore, in this work we demonstrate that at physiological pH, Tyr2 undergoes oxidation upon UV excitation yielding different products which conserve the dimeric structure. During its photodegradation different reactive oxygen species, like hydrogen peroxide, superoxide anion and singlet oxygen, are produced. Otherwise, we demonstrated that Tyr2 is able to sensitize the photodegradation of tyrosine. The results presented in this work confirm that Tyr2 can act as a potential photosensitizer, contributing to the harmful effects of UV-A radiation on biological systems.

Identifiants

pubmed: 31070216
doi: 10.1039/c9pp00182d
doi:

Substances chimiques

Proteins 0
Reactive Oxygen Species 0
Superoxides 11062-77-4
Tyrosine 42HK56048U
Hydrogen Peroxide BBX060AN9V

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1732-1741

Auteurs

Lara O Reid (LO)

Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Departamento de Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, CCT La Plata-CONICET. Casilla de Correo 16, Sucursal 4, (1900) La Plata, Argentina. ldantola@inifta.unlp.edu.ar.

Mariana Vignoni (M)

Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Departamento de Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, CCT La Plata-CONICET. Casilla de Correo 16, Sucursal 4, (1900) La Plata, Argentina. ldantola@inifta.unlp.edu.ar.

Nathalie Martins-Froment (N)

Service Commun de Spectrométrie de Masse (FR2599), Université de Toulouse III (Paul Sabatier), 118, route de Narbonne, F-31062 Toulouse cédex 9, France.

Andrés H Thomas (AH)

Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Departamento de Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, CCT La Plata-CONICET. Casilla de Correo 16, Sucursal 4, (1900) La Plata, Argentina. ldantola@inifta.unlp.edu.ar.

M Laura Dántola (ML)

Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Departamento de Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, CCT La Plata-CONICET. Casilla de Correo 16, Sucursal 4, (1900) La Plata, Argentina. ldantola@inifta.unlp.edu.ar.

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Classifications MeSH