Modification-specific proteomics: Strategies for characterization of post-translational modifications using enrichment techniques

被引:270
作者
Zhao, Yingming [1 ]
Jensen, Ole N. [2 ]
机构
[1] Univ Chicago, Ben May Dept Canc Res, Chicago, IL 60637 USA
[2] Univ So Denmark, Dept Biochem & Mol Biol, Prot Res Grp, Odense, Denmark
关键词
Affinity chromatography; Microbiology; MS; Post-translational modification; GLCNAC-MODIFIED PROTEINS; N-LINKED GLYCOPROTEINS; SITE-SPECIFIC PHOSPHORYLATION; TANDEM MASS-SPECTROMETRY; LARGE-SCALE ANALYSIS; SACCHAROMYCES-CEREVISIAE; AFFINITY-CHROMATOGRAPHY; IN-VIVO; MEMBRANE-PROTEINS; PLASMA-MEMBRANE;
D O I
10.1002/pmic.200900398
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
More than 300 different types of protein post-translational modifications (PTMs) have been described, many of which are known to have pivotal roles in cellular physiology and disease. Nevertheless, only a handful of PTMs have been extensively investigated at the proteome level. Knowledge of protein substrates and their PTM sites is key to dissection of PTM-mediated cellular processes. The past several years have seen a tremendous progress in developing MS-based proteomics technologies for global PTM analysis, including numerous studies of yeast and other microbes. Modification-specific enrichment techniques combined with advanced MS/MS methods and computational data analysis have revealed a surprisingly large extent of PTMs in proteins, including multi-site, cooperative modifications in individual proteins. We review some of the current strategies employed for enrichment and detection of PTMs in modification-specific proteomics.
引用
收藏
页码:4632 / 4641
页数:10
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