Oxidation proteomics: the role of thiol modifications

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Etat: Public
Version: de l'auteur⸱e
ID Serval
serval:BIB_F23E1D0CEB06
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Oxidation proteomics: the role of thiol modifications
Périodique
Current Proteomics
Auteur⸱e⸱s
Riederer B.M
ISSN
1570-1646
Statut éditorial
Publié
Date de publication
2009
Volume
6
Numéro
1
Pages
51-62
Langue
anglais
Résumé
Identification of thiol modifications has gained significant importance. It is increasingly recognized that cysteines play an important role in protein function under both physiological and patho-physiological conditions. Here we reviewed different approaches that are used to identify oxidized proteins and discuss different fluorescent labeling techniques, differential two-dimensional gel electrophoresis and matrix-assisted laser desorption ionization - time of flight identification, in short MALDI-TOF. We illuminate processes that depend on protein oxidation of cysteines and we look into consequences of thiol oxidation during aging and in a variety of diseases, with a special reference to Alzheimer's disease. There is an urgent need for methods that detect specifically oxidized proteins and are able to distinguish different oxidation types.
Mots-clé
Aging , cysteine , oxidation , thiol , DIGE , MALDI-TOF , Western blot , dye labeling , disease
Web of science
Création de la notice
23/08/2010 14:24
Dernière modification de la notice
20/08/2019 17:19
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