Technologies and challenges in large-scale phosphoproteomics.

Proteomics

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.

Published: March 2013

Phosphorylation, the reversible addition of a phosphate group to amino acid side chains of proteins, is a fundamental regulator of protein activity, stability, and molecular interactions. Most cellular processes, such as inter- and intracellular signaling, protein synthesis, degradation, and apoptosis, rely on phosphorylation. This PTM is thus involved in many diseases, rendering localization and assessment of extent of phosphorylation of major scientific interest. MS-based phosphoproteomics, which aims at describing all phosphorylation sites in a specific type of cell, tissue, or organism, has become the main technique for discovery and characterization of phosphoproteins in a nonhypothesis driven fashion. In this review, we describe methods for state-of-the-art MS-based analysis of protein phosphorylation as well as the strategies employed in large-scale phosphoproteomic experiments with focus on the various challenges and limitations this field currently faces.

Download full-text PDF

Source
http://dx.doi.org/10.1002/pmic.201200484DOI Listing

Publication Analysis

Top Keywords

phosphorylation
5
technologies challenges
4
challenges large-scale
4
large-scale phosphoproteomics
4
phosphoproteomics phosphorylation
4
phosphorylation reversible
4
reversible addition
4
addition phosphate
4
phosphate group
4
group amino
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!