Pathway discovery by genome-wide, high-throughput, quantitative mass spectrometry

被引:0
作者
Jin, Shuangshuang [1 ]
Suleiman, Atef [1 ]
Daly, Donald [2 ]
Springer, David [2 ]
Miller, John [1 ]
机构
[1] Washington State Univ Tri Cities, Richland, WA 99352 USA
[2] Pacific NW Natl Lab, Richland, WA 99352 USA
来源
2008 IEEE INTERNATIONAL WORKSHOP ON GENOMIC SIGNAL PROCESSING AND STATISTICS | 2008年
关键词
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中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Genome-wide high-throughput mass spectrometry has emerged as an important new source of data on biological systems. This technology yields global information about the proteins expressed by an organism; consequently, biological processes can be studied without prior assumptions about the proteins that are involved. A profile of up- and down-regulated proteins is obtained which can be used to discover the gene-expression and cellular signaling pathways that underlie disease states and/or responses to treatments. Many data-manipulation steps are involved in obtaining pathway information from mass spectrometry of protease-digested complex mixtures of proteins. In this paper, we describe work to create a seamless data flow through these steps from peptide detection to queries of pathway databases based on patterns of up- and down-regulated proteins. Data from a mouse-model study of chronic obstructive pulmonary disease (COPD) are used to illustrate our results.
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页码:3 / +
页数:2
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