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
[31]   DEAMIDATION OF SOLUBLE CD4 AT ASPARAGINE-52 RESULTS IN REDUCED BINDING-CAPACITY FOR THE HIV-1 ENVELOPE GLYCOPROTEIN GP120 [J].
TESHIMA, G ;
PORTER, J ;
YIM, K ;
LING, V ;
GUZZETTA, A .
BIOCHEMISTRY, 1991, 30 (16) :3916-3922
[32]   From genomics to proteomics [J].
Tyers, M ;
Mann, M .
NATURE, 2003, 422 (6928) :193-197
[33]   Quantification of proteins and metabolites by mass spectrometry without isotopic labeling or spiked standards [J].
Wang, WX ;
Zhou, HH ;
Lin, H ;
Roy, S ;
Shaler, TA ;
Hill, LR ;
Norton, S ;
Kumar, P ;
Anderle, M ;
Becker, CH .
ANALYTICAL CHEMISTRY, 2003, 75 (18) :4818-4826
[34]   Large-scale analysis of the yeast proteome by multidimensional protein identification technology [J].
Washburn, MP ;
Wolters, D ;
Yates, JR .
NATURE BIOTECHNOLOGY, 2001, 19 (03) :242-247
[35]   Analysis of quantitative proteomic data generated via multidimensional protein identification technology [J].
Washburn, MP ;
Ulaszek, R ;
Deciu, C ;
Schieltz, DM ;
Yates, JR .
ANALYTICAL CHEMISTRY, 2002, 74 (07) :1650-1657
[36]   Isotopic deconvolution of matrix-assisted laser desorption/ionization mass spectra for substance-class specific analysis of complex samples [J].
Wehofsky, M ;
Hoffmann, R ;
Hubert, M ;
Spengler, B .
EUROPEAN JOURNAL OF MASS SPECTROMETRY, 2001, 7 (01) :39-46
[37]   Proteolytic 18O labeling for comparative proteomics:: Model studies with two serotypes of adenovirus [J].
Yao, XD ;
Freas, A ;
Ramirez, J ;
Demirev, PA ;
Fenselau, C .
ANALYTICAL CHEMISTRY, 2001, 73 (13) :2836-2842
[38]   Microfluidic chip for peptide analysis with an integrated HPLC column, sample enrichment column, and nanoelectrospray tip [J].
Yin, NF ;
Killeen, K ;
Brennen, R ;
Sobek, D ;
Werlich, M ;
van de Goor, TV .
ANALYTICAL CHEMISTRY, 2005, 77 (02) :527-533
[39]   Identification and quantification of N-linked glycoproteins using hydrazide chemistry, stable isotope labeling and mass spectrometry [J].
Zhang, H ;
Li, XJ ;
Martin, DB ;
Aebersold, R .
NATURE BIOTECHNOLOGY, 2003, 21 (06) :660-666
[40]   Energy transfer electrogenerated chemiluminescence for the determination of sulfite [J].
Zhang, MN ;
Zhang, CX ;
Qi, HL .
MICROCHIMICA ACTA, 2004, 144 (1-3) :155-160