Literature DB >> 17172690

Proteomic identification of S-nitrosylated proteins in endothelial cells.

Antonio Martínez-Ruiz1, Santiago Lamas.   

Abstract

Nitric oxide (NO) produced in endothelial cells exerts important roles in the vascular system. In recent years, posttranslational modifications induced by NO have been increasingly studied and, among them, cysteine modification by S-nitrosylation (also called S-nitrosation) has been hypothesized to represent a relevant mechanism for cell signaling. Thus, knowledge of the proteins that can be S-nitrosylated in endothelial cells will help to better understand the possible role of this modification. We describe a protocol to identify the S-nitrosylome or S-nitrosoproteome of endothelial cells, based on the specific derivatization of the S-nitrosylation, substituting it by a biotinylation, and the purification of the biotinylated proteins.

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Year:  2007        PMID: 17172690     DOI: 10.1385/1-59745-214-9:215

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  8 in total

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3.  S-nitrosylation of phosphotransfer proteins represses cytokinin signaling.

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4.  Nitrate reductase mediates nitric oxide-dependent gravitropic response in Arabidopsis thaliana roots.

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5.  Comprehensive identification and modified-site mapping of S-nitrosylated targets in prostate epithelial cells.

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Journal:  PLoS One       Date:  2010-02-05       Impact factor: 3.240

Review 6.  Radical-free biology of oxidative stress.

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7.  The Redox System in C. elegans, a Phylogenetic Approach.

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Journal:  J Toxicol       Date:  2012-07-31

8.  Distribution of Endogenous NO Regulates Early Gravitropic Response and PIN2 Localization in Arabidopsis Roots.

Authors:  Ramiro París; María M Vazquez; Magdalena Graziano; María C Terrile; Nathan D Miller; Edgar P Spalding; Marisa S Otegui; Claudia A Casalongué
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  8 in total

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