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Artículo

Photo-tuneable protein nitration by sensitiser tris(bipyridine)-Ruthenium(II) chloride complex

Giménez, EzequielIcon ; Urlaub, Henning; Falomir Lockhart, Lisandro JorgeIcon
Fecha de publicación: 12/2022
Editorial: Academic Press Inc Elsevier Science
Revista: Nitric Oxide-Biology and Chemistry
ISSN: 1089-8603
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Biofísica

Resumen

Post-translational modifications (PTMs) of proteins are a diverse source of variability that impacts on their functions, localisation, regulation, and lifetime. However, one of the main pitfalls in their study is that they appear in rather low frequencies and/or are only transiently observed. To overcome this issue and ease the study in vitro of stress-related protein PTMs, several methods have been proposed to model stress conditions and chemically introduce them. These techniques employ the combination of peroxides with transition metal ions or haem-containing proteins, as well as other possibilities such as peroxy radicals or UV radiation. However, their control, reproducibility and undesired secondary reactions that reduce the process yield are often a matter of concern. Here we introduce a photo-tuneable method that selectively targets nitration of aromatic residues. We initially present the adaptation of an oxidation method based on the photosensitiser tris(2,2′-bipyridine)-Ruthenium(II) chloride complex and ammonium persulfate, in which we employ an alternative radical neutralisation/trapping pathway that uses nitrite ions for the nitration of free L-Tyrosine and L-Tryptophan amino acids. After analysing the effect of several factors, we report the application of the photo-tuneable protein nitration (PTPN) method to four different model proteins in which we evaluate the nitration and oxidation of residues in each case. A mass spectrometry label-free quantitation of Tyr and Trp nitration is also described in order to compare the degree of modification and the accessibility of these residues. The method described could be employed to scale up the production of proteins with a selected range of oxidative PTMs for their characterisation, the assessment of their pathophysiological roles, and the development of detection and quantification methods to validate these PTMs as novel biomarkers associated with oxidative stress-related pathologies, such as in cardiovascular or neurodegenerative diseases.
Palabras clave: NITRO-TYROSINE , NITROSATIVE STRESS , OXIDATIVE STRESS , PHOTOCHEMISTRY , PHOTOSENSITISER , PROTEIN POST-TRANSLATIONAL MODIFICATIONS
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info:eu-repo/semantics/restrictedAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/212499
URL: https://www.sciencedirect.com/science/article/pii/S1089860322001100
DOI: https://doi.org/10.1016/j.niox.2022.10.002
Colecciones
Articulos(INIBIOLP)
Articulos de INST.DE INVEST.BIOQUIMICAS DE LA PLATA
Citación
Giménez, Ezequiel; Urlaub, Henning; Falomir Lockhart, Lisandro Jorge; Photo-tuneable protein nitration by sensitiser tris(bipyridine)-Ruthenium(II) chloride complex; Academic Press Inc Elsevier Science; Nitric Oxide-Biology and Chemistry; 129; 12-2022; 63-73
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