Detection and proteomic identification of S-nitrosated proteins in human hepatocytes
Keywords: 
Hepatocytes/metabolism
Proteins/analysis
Proteins/metabolism
Proteomics/methods
S-Nitrosothiols/analysis
S-Nitrosothiols/metabolism
Issue Date: 
2008
Publisher: 
Elsevier
ISSN: 
1557-7988
Citation: 
Lopez-Sanchez LM, Corrales FJ, De La Mata M, Muntane J, Rodriguez-Ariza A. Detection and proteomic identification of S-nitrosated proteins in human hepatocytes. Methods Enzymol 2008;440:273-281.
Abstract
The S-nitrosation of protein thiols is a redox-based posttranslational modification that modulates protein function and cell phenotype. Although the detection of S-nitrosated proteins is problematical because of the lability of S-nitrosothiols, an increasing range of proteins has been shown to undergo S-nitrosation with the improvement of molecular tools. This chapter describes the methodology used to identify potential targets of S-nitrosation in cultured primary human hepatocytes using proteomic approaches. This methodology is based on the biotin switch method, which labels S-nitrosated proteins with an affinity tag, allowing their selective detection and proteomic identification.

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