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Mass spectrometric analysis of protein tyrosine nitration in aging and neurodegenerative diseases

journal contribution
posted on 2015-03-01, 00:00 authored by Woon-Seok Yeo, Young Jun Kim, Mohammad Humayun Kabir, Jeong Won Kang, Md Ahsan Ul Bari, Kwang Pyo Kim
This review highlights the significance of protein tyrosine nitration (PTN) in signal transduction pathways, the progress achieved in analytical methods, and the implication of nitration in the cellular pathophysiology of aging and age‐related neurodegenerative diseases. Although mass spectrometry of nitrated peptides has become a powerful tool for the characterization of nitrated peptides, the low stoichiometry of this modification clearly necessitates the use of affinity chromatography to enrich modified peptides. Analysis of nitropeptides involves identification of endogenous, intact modification as well as chemical conversion of the nitro group to a chemically reactive amine group and further modifications that enable affinity capture and enhance detectability by altering molecular properties. In this review, we focus on the recent progress in chemical derivatization of nitropeptides for enrichment and mass analysis, and for detection and quantification using various analytical tools. PTN participates in physiological processes, such as aging and neurodegenerative diseases. Accumulation of 3‐nitrotyrosine has been found to occur during the aging process; this was identified through mass spectrometry. Further, there are several studies implicating the presence of nitrated tyrosine in age‐related diseases such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis.

History

Journal

Mass spectrometry reviews

Volume

34

Season

Mar/Apr

Pagination

166-183

Location

Chichester, Eng.

ISSN

0277-7037

Language

eng

Publication classification

C1.1 Refereed article in a scholarly journal

Copyright notice

2014, Wiley Periodicals, Inc.

Issue

2

Publisher

John Wiley & Sons