Advances in proteomic workflows for systems biology

被引:78
作者
Malmstroem, Johan
Lee, Hookeun
Aebersold, Ruedi [1 ]
机构
[1] ETH, Inst Mol Syst Biol, Zurich, Switzerland
[2] Univ Zurich, Fac Sci, Zurich, Switzerland
[3] Inst Syst Biol, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.copbio.2007.07.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mass spectrometry, specifically the analysis of complex peptide mixtures by liquid chromatography and tandem mass spectrometry (shotgun proteomics) has been at the centre of proteomics research for the past decade. To overcome some of the fundamental limitations of the approach, including its limited sensitivity and high degree of redundancy, new proteomic workflows are being developed. Among these, targeting methods in which specific peptides are selectively isolated, identified and quantified are particularly promising. Here we summarize recent incremental advances in shotgun proteomic methods and outline emerging targeted workflows. The development of the target-driven approaches with their ability to detect and quantify identical, non-redundant sets of proteins in multiple repeat analyses will be crucially important for the application of proteomics to biomarker discovery and validation, and. to systems biology research.
引用
收藏
页码:378 / 384
页数:7
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