Evaluation of proteomic strategies for analyzing ubiquitinated proteins

被引:34
作者
Peng, Junmin [1 ]
机构
[1] Emory Univ, Sch Med, Dept Human Genet, Ctr Neurodegenerat Dis, Atlanta, GA 30322 USA
关键词
affinity chromatography; mass spectrometry; middle-down; proteomics; ubiquitin;
D O I
10.5483/BMBRep.2008.41.3.177
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ubiquitin is an essential, highly-conserved small regulatory protein in eukaryotic cells. It covalently modifies a wide variety of targeted proteins in the forms of monomer and polymers, altering the conformation and binding properties of the proteins and thus regulating proteasomal delivery, protein activities and localization. Mass spectrometry has emerged as an indispensable tool for in-depth characterization of protein ubiquitination. Ubiquitinated proteins in cell lysates are usually enriched by affinity chromatography and subsequently analyzed by mass spectrometry for identification and quantification. Ubiquitin-conjugated amino acid residues can be determined by unique mass shift caused by the modification. Moreover, the complex structure of polyubiquitin chains on substrates can be dissected by bottom-up and middle-down mass spectrometric approaches, revealing potential novel functions of polyubiquitin linkages. Here I review the advances and caveats of these strategies, emphasizing caution in the validation of ubiquitinated proteins and in the interpretation of raw data.
引用
收藏
页码:177 / 183
页数:7
相关论文
共 52 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]   Global changes to the ubiquitin system in Huntington's disease [J].
Bennett, Eric J. ;
Shaler, Thomas A. ;
Woodman, Ben ;
Ryu, Kwon-Yul ;
Zaitseva, Tatiana S. ;
Becker, Christopher H. ;
Bates, Gillian P. ;
Schulman, Howard ;
Kopito, Ron R. .
NATURE, 2007, 448 (7154) :704-U11
[3]   Ubiquitination on nonlysine residues by a viral E3 ubiquitin ligase [J].
Cadwell, K ;
Coscoy, L .
SCIENCE, 2005, 309 (5731) :127-130
[4]   N-terminal ubiquitination: more protein substrates join in [J].
Ciechanover, A ;
Ben-Saadon, R .
TRENDS IN CELL BIOLOGY, 2004, 14 (03) :103-106
[5]   Ubiquitin chains are remodeled at the proteasome by opposing ubiquitin ligase and deubiquitinating activities [J].
Crosas, Bernat ;
Hanna, John ;
Kirkpatrick, Donald S. ;
Zhang, Dan Phoebe ;
Tone, Yoshiko ;
Hathaway, Nathaniel A. ;
Buecker, Christa ;
Leggett, David S. ;
Schmidt, Marion ;
King, Randall W. ;
Gygi, Steven P. ;
Finley, Daniel .
CELL, 2006, 127 (07) :1401-1413
[6]   Tryptic digestion of ubiquitin standards reveals an improved strategy for identifying ubiquitinated proteins by mass spectrometry [J].
Denis, Nicholas J. ;
Vasilescu, Julian ;
Lambert, Jean-Philippe ;
Smith, Jeffrey C. ;
Figeys, Daniel .
PROTEOMICS, 2007, 7 (06) :868-874
[7]   Characterization of neurohistone variants and post-translational modifications by electron capture dissociation mass spectrometry [J].
Garcia, Benjamin A. ;
Siuti, Nertila ;
Thomas, C. Eric ;
Mizzen, Craig A. ;
Kelleher, Neil L. .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2007, 259 (1-3) :184-196
[8]   Structural complexity in ubiquitin recognition [J].
Harper, JW ;
Schulman, BA .
CELL, 2006, 124 (06) :1133-1136
[9]   Ubiquitin-binding domains [J].
Hicke, L ;
Schubert, HL ;
Hill, CP .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (08) :610-621
[10]   A subset of membrane-associated proteins is ubiquitinated in response to mutations in the endoplasmic reticulum degradation machinery [J].
Hitchcock, AL ;
Auld, K ;
Gygi, SP ;
Silver, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (22) :12735-12740