Analytical strategies for phosphoproteomics

被引:370
作者
Thingholm, Tine E. [1 ,2 ]
Jensen, Ole N. [2 ]
Larsen, Martin R. [2 ]
机构
[1] Odense Univ Hosp, Dept Endocrinol, KMEB, DK-5000 Odense M, Denmark
[2] Univ So Denmark, Dept Biochem & Mol Biol, Odense M, Denmark
关键词
Affinity enrichment; Cell signaling; Immunoaffinity chromatography; SIMAC; Titanium dioxide chromatography; TANDEM MASS-SPECTROMETRY; ION AFFINITY-CHROMATOGRAPHY; GROWTH-FACTOR RECEPTOR; ANION-EXCHANGE CHROMATOGRAPHY; ELECTRON-CAPTURE DISSOCIATION; SITE-SPECIFIC PHOSPHORYLATION; HIGHLY SELECTIVE ENRICHMENT; PROTEIN-PHOSPHORYLATION; TYROSINE PHOSPHORYLATION; PROTEOMIC ANALYSIS;
D O I
10.1002/pmic.200800454
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein phosphorylation is a key regulator of cellular signaling pathways. It is involved in most cellular events in which the complex interplay between protein kinases and protein phosphatases strictly controls biological processes such as proliferation, differentiation, and apoptosis. Defective or altered signaling pathways often result in abnormalities leading to various diseases, emphasizing the importance of understanding protein phosphorylation. Phosphorylation is a transient modification, and phosphoproteins are often very low abundant. Consequently, phosphoproteome analysis requires highly sensitive and specific strategies. Today, most phosphoproteomic studies are conducted by mass spectrometric strategies in combination with phospho-specific enrichment methods. This review presents an overview of different analytical strategies for the characterization of phosphoproteins. Emphasis will be on the affinity methods utilized specifically for phosphoprotein and phosphopeptide enrichment prior to MS analysis, and on recent applications of these methods in cell biological applications.
引用
收藏
页码:1451 / 1468
页数:18
相关论文
共 132 条
[1]   HYDROPHILIC-INTERACTION CHROMATOGRAPHY FOR THE SEPARATION OF PEPTIDES, NUCLEIC-ACIDS AND OTHER POLAR COMPOUNDS [J].
ALPERT, AJ .
JOURNAL OF CHROMATOGRAPHY, 1990, 499 :177-196
[2]   ISOLATION OF PHOSPHOPROTEINS BY IMMOBILIZED METAL (FE-3+) AFFINITY-CHROMATOGRAPHY [J].
ANDERSSON, L ;
PORATH, J .
ANALYTICAL BIOCHEMISTRY, 1986, 154 (01) :250-254
[3]  
[Anonymous], 52 ASMS C MASS SPECT
[4]   Limitations to the comparative proteomic analysis of thrombopoietin producing Chinese hamster ovary cells treated with sodium butyrate [J].
Baik, Jong Youn ;
Joo, Eun Jin ;
Kim, Young Hwan ;
Lee, Gyun Min .
JOURNAL OF BIOTECHNOLOGY, 2008, 133 (04) :461-468
[5]   Quantitative mass spectrometry in proteomics: a critical review [J].
Bantscheff, Marcus ;
Schirle, Markus ;
Sweetman, Gavain ;
Rick, Jens ;
Kuster, Bernhard .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2007, 389 (04) :1017-1031
[6]   Large-scale characterization of HeLa cell nuclear phosphoproteins [J].
Beausoleil, SA ;
Jedrychowski, M ;
Schwartz, D ;
Elias, JE ;
Villén, J ;
Li, JX ;
Cohn, MA ;
Cantley, LC ;
Gygi, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (33) :12130-12135
[7]   Quantitative phosphoproteomics of early elicitor signaling in Arabidopsis [J].
Benschop, Joris J. ;
Mohammed, Shabaz ;
O'Flaherty, Martina ;
Heck, Albert J. R. ;
Slijper, Monique ;
Menke, Frank L. H. .
MOLECULAR & CELLULAR PROTEOMICS, 2007, 6 (07) :1198-1214
[8]   CONTRIBUTIONS OF MASS-SPECTROMETRY TO PEPTIDE AND PROTEIN-STRUCTURE [J].
BIEMANN, K .
BIOMEDICAL AND ENVIRONMENTAL MASS SPECTROMETRY, 1988, 16 (1-12) :99-111
[9]   An integrated chemical, mass spectrometric and computational strategy for (quantitative) phosphoproteomics:: application to Drosophila melanogaster Kc167 cells [J].
Bodenmiller, Bernd ;
Mueller, Lukas N. ;
Pedrioli, Patrick G. A. ;
Pflieger, Delphine ;
Juenger, Martin A. ;
Eng, Jimmy K. ;
Aebersold, Ruedi ;
Tao, W. Andy .
MOLECULAR BIOSYSTEMS, 2007, 3 (04) :275-286
[10]   Reproducible isolation of distinct, overlapping segments of the phosphoproteome [J].
Bodenmiller, Bernd ;
Mueller, Lukas N. ;
Mueller, Markus ;
Domon, Bruno ;
Aebersold, Ruedi .
NATURE METHODS, 2007, 4 (03) :231-237