Network-based inference from complex proteomic mixtures using SNIPE

被引:10
作者
Nusinow, David P. [1 ]
Kiezun, Adam [1 ]
O'Connell, Daniel J. [1 ]
Chick, Joel M. [2 ]
Yue, Yingzi [1 ]
Maas, Richard L. [1 ]
Gygi, Steven P. [2 ]
Sunyaev, Shamil R. [1 ]
机构
[1] Brigham & Womens Hosp, Div Genet, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
MASS-SPECTROMETRY; PROTEIN ABUNDANCE; SCALE; QUANTIFICATION; ASSOCIATION; EXPRESSION; BIOLOGY; SYSTEMS; GENES; YEAST;
D O I
10.1093/bioinformatics/bts594
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Proteomics presents the opportunity to provide novel insights about the global biochemical state of a tissue. However, a significant problem with current methods is that shotgun proteomics has limited success at detecting many low abundance proteins, such as transcription factors from complex mixtures of cells and tissues. The ability to assay for these proteins in the context of the entire proteome would be useful in many areas of experimental biology. Results: We used network-based inference in an approach named SNIPE (Software for Network Inference of Proteomics Experiments) that selectively highlights proteins that are more likely to be active but are otherwise undetectable in a shotgun proteomic sample. SNIPE integrates spectral counts from paired case-control samples over a network neighbourhood and assesses the statistical likelihood of enrichment by a permutation test. As an initial application, SNIPE was able to select several proteins required for early murine tooth development. Multiple lines of additional experimental evidence confirm that SNIPE can uncover previously unreported transcription factors in this system. We conclude that SNIPE can enhance the utility of shotgun proteomics data to facilitate the study of poorly detected proteins in complex mixtures.
引用
收藏
页码:3115 / 3122
页数:8
相关论文
共 27 条
[1]  
[Anonymous], 2011, R: A Language and Environment for Statistical Computing
[2]  
[Anonymous], 2006, INT J COMPLEX SYST
[3]   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
[4]   Molecular genetics of tooth development [J].
Bei, Marianna .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2009, 19 (05) :504-510
[5]   Tissue specificity and the human protein interaction network [J].
Bossi, Alice ;
Lehner, Ben .
MOLECULAR SYSTEMS BIOLOGY, 2009, 5
[6]   The Mouse Genome Database (MGD): mouse biology and model systems [J].
Bult, Carol J. ;
Eppig, Janan T. ;
Kadin, James A. ;
Richardson, Joel E. ;
Blake, Judith A. .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D724-D728
[7]   Comprehensive mass-spectrometry-based proteome quantification of haploid versus diploid yeast [J].
de Godoy, Lyris M. F. ;
Olsen, Jesper V. ;
Cox, Juergen ;
Nielsen, Michael L. ;
Hubner, Nina C. ;
Froehlich, Florian ;
Walther, Tobias C. ;
Mann, Matthias .
NATURE, 2008, 455 (7217) :1251-U60
[8]   Interpreting Metabolomic Profiles using Unbiased Pathway Models [J].
Deo, Rahul C. ;
Hunter, Luke ;
Lewis, Gregory D. ;
Pare, Guillaume ;
Vasan, Ramachandran S. ;
Chasman, Daniel ;
Wang, Thomas J. ;
Gerszten, Robert E. ;
Roth, Frederick P. .
PLOS COMPUTATIONAL BIOLOGY, 2010, 6 (02)
[9]   Chemogenomic profiling on a genomewide scale using reverse-engineered gene networks [J].
di Bernardo, D ;
Thompson, MJ ;
Gardner, TS ;
Chobot, SE ;
Eastwood, EL ;
Wojtovich, AP ;
Elliott, SJ ;
Schaus, SE ;
Collins, JJ .
NATURE BIOTECHNOLOGY, 2005, 23 (03) :377-383
[10]   lumi:: a pipeline for processing Illumina microarray [J].
Du, Pan ;
Kibbe, Warren A. ;
Lin, Simon M. .
BIOINFORMATICS, 2008, 24 (13) :1547-1548