A software suite for the generation and comparison of peptide arrays from sets of data collected by liquid chromatography-mass spectrometry

被引:142
作者
Li, XJ
Yi, EC
Kemp, CJ
Zhang, H
Aebersold, R
机构
[1] Inst Syst Biol, Seattle, WA 98103 USA
[2] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[3] Swiss Fed Inst Technol, Inst Mol Syst Biol, CH-8093 Zurich, Switzerland
[4] Univ Zurich, Fac Nat Sci, CH-8093 Zurich, Switzerland
关键词
D O I
10.1074/mcp.M500141-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
There is an increasing interest in the quantitative proteomic measurement of the protein contents of substantially similar biological samples, e. g. for the analysis of cellular response to perturbations over time or for the discovery of protein biomarkers from clinical samples. Technical limitations of current proteomic platforms such as limited reproducibility and low throughput make this a challenging task. A new LC-MS-based platform is able to generate complex peptide patterns from the analysis of proteolyzed protein samples at high throughput and represents a promising approach for quantitative proteomics. A crucial component of the LC-MS approach is the accurate evaluation of the abundance of detected peptides over many samples and the identification of peptide features that can stratify samples with respect to their genetic, physiological, or environmental origins. We present here a new software suite, SpecArray, that generates a peptide versus sample array from a set of LC-MS data. A peptide array stores the relative abundance of thousands of peptide features in many samples and is in a format identical to that of a gene expression microarray. A peptide array can be subjected to an unsupervised clustering analysis to stratify samples or to a discriminant analysis to identify discriminatory peptide features. We applied the SpecArray to analyze two sets of LC-MS data: one was from four repeat LC-MS analyses of the same glycopeptide sample, and another was from LC-MS analysis of serum samples of five male and five female mice. We demonstrate through these two study cases that the SpecArray software suite can serve as an effective software platform in the LC-MS approach for quantitative proteomics.
引用
收藏
页码:1328 / 1340
页数:13
相关论文
共 40 条
[1]   Toward a human blood serum proteome - Analysis by multidimensional separation coupled with mass spectrometry [J].
Adkins, JN ;
Varnum, SM ;
Auberry, KJ ;
Moore, RJ ;
Angell, NH ;
Smith, RD ;
Springer, DL ;
Pounds, JG .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (12) :947-955
[2]   Mass spectrometry in proteomics [J].
Aebersold, R ;
Goodlett, DR .
CHEMICAL REVIEWS, 2001, 101 (02) :269-295
[3]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[4]   Temporal analysis of phosphotyrosine-dependent signaling networks by quantitative proteomics [J].
Blagoev, B ;
Ong, SE ;
Kratchmarova, I ;
Mann, M .
NATURE BIOTECHNOLOGY, 2004, 22 (09) :1139-1145
[5]   A proteomics strategy to elucidate functional protein-protein interactions applied to EGF signaling [J].
Blagoev, B ;
Kratchmarova, I ;
Ong, SE ;
Nielsen, M ;
Foster, LJ ;
Mann, M .
NATURE BIOTECHNOLOGY, 2003, 21 (03) :315-318
[6]   Biomedical informatics for proteomics [J].
Boguski, MS ;
McIntosh, MW .
NATURE, 2003, 422 (6928) :233-237
[7]   Identification and relative quantitation of protein mixtures by enzymatic digestion followed by capillary reversed-phase liquid chromatography-tandem mass spectrometry [J].
Bondarenko, PV ;
Chelius, D ;
Shaler, TA .
ANALYTICAL CHEMISTRY, 2002, 74 (18) :4741-4749
[8]  
COIFMAN R. R., 1995, Wavelets and statistics, P125, DOI DOI 10.1007/978-1-4612-2544-7_9
[9]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[10]   AN APPROACH TO CORRELATE TANDEM MASS-SPECTRAL DATA OF PEPTIDES WITH AMINO-ACID-SEQUENCES IN A PROTEIN DATABASE [J].
ENG, JK ;
MCCORMACK, AL ;
YATES, JR .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (11) :976-989