Mass Spectrometry-Based Proteomics and Network Biology

被引:304
作者
Bensimon, Ariel [1 ,2 ]
Heck, Albert J. R. [1 ,3 ,4 ]
Aebersold, Ruedi [1 ,2 ,5 ]
机构
[1] ETH, Dept Biol, Inst Mol Syst Biol, CH-8093 Zurich, Switzerland
[2] ETH, Competence Ctr Syst Physiol & Metab Dis, CH-8093 Zurich, Switzerland
[3] Univ Utrecht, NL-3584 CH Utrecht, Netherlands
[4] Netherlands Prote Ctr, NL-3584 CH Utrecht, Netherlands
[5] Univ Zurich, Fac Sci, CH-8006 Zurich, Switzerland
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 81 | 2012年 / 81卷
关键词
systems biology; quantitative proteomics; protein interaction network; protein-signaling network; posttranslational modification; data-driven modeling; QUANTITATIVE INTERACTION PROTEOMICS; PROTEIN-INTERACTION NETWORKS; LARGE-SCALE; PHOSPHOPROTEOMIC ANALYSIS; ABSOLUTE QUANTIFICATION; SYSTEMS BIOLOGY; SIGNALING NETWORKS; LC-MS; KINASE; REVEALS;
D O I
10.1146/annurev-biochem-072909-100424
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
In the life sciences, a new paradigm is emerging that places networks of interacting molecules between genotype and phenotype. These networks are dynamically modulated by a multitude of factors, and the properties emerging from the network as a whole determine observable phenotypes. This paradigm is usually referred to as systems biology, network biology, or integrative biology. Mass spectrometry (MS)-based proteomics is a central life science technology that has realized great progress toward the identification, quantification, and characterization of the proteins that constitute a proteome. Here, we review how MS-based proteomics has been applied to network biology to identify the nodes and edges of biological networks, to detect and quantify perturbation-induced network changes, and to correlate dynamic network rewiring with the cellular phenotype. We discuss future directions for MS-based proteomics within the network biology paradigm.
引用
收藏
页码:379 / 405
页数:27
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