Protein 3-nitrotyrosine in complex biological samples: quantification by high-pressure liquid chromatography/electrochemical detection and emergence of proteomic approaches for unbiased identification of modification sites. Article uri icon

Overview

abstract

  • Nitration of tyrosine residues by nitric oxide (NO)-derived species results in the accumulation of 3-nitrotyrosine in proteins, a hallmark of nitrosative stress in cells and tissues. Tyrosine nitration is recognized as one of the multiple signaling modalities used by NO-derived species for the regulation of protein structure and function in health and disease. Various methods have been described for the quantification of protein 3-nitrotyrosine residues, and several strategies have been presented toward the goal of proteome-wide identification of protein tyrosine modification sites. This chapter details a useful protocol for the quantification of 3-nitrotyrosine in cells and tissues using high-pressure liquid chromatography with electrochemical detection. Additionally, this chapter describes a novel biotin-tagging strategy for specific enrichment of 3-nitrotyrosine-containing peptides. Application of this strategy, in conjunction with high-throughput MS/MS-based peptide sequencing, is anticipated to fuel efforts in developing comprehensive inventories of nitrosative stress-induced protein-tyrosine modification sites in cells and tissues.

publication date

  • January 1, 2008

Research

keywords

  • Complex Mixtures
  • Electrochemistry
  • Proteins
  • Proteomics
  • Tandem Mass Spectrometry
  • Tyrosine

Identity

PubMed Central ID

  • PMC2483310

Scopus Document Identifier

  • 52249115847

Digital Object Identifier (DOI)

  • 10.1016/S0076-6879(08)01201-9

PubMed ID

  • 18554526

Additional Document Info

volume

  • 441