A Proteome Catalog of Drosophila melanogaster -: An essential resource for targeted quantitative proteomics

被引:13
作者
Ahrens, Christian H. [1 ,2 ]
Brunner, Erich [1 ,3 ]
Hafen, Ernst [4 ]
Aebersold, Ruedi [4 ,5 ]
Basler, Konrad [1 ,3 ]
机构
[1] Univ Zurich, Ctr Model Organism Proteomes, CH-8057 Zurich, Switzerland
[2] Univ Zurich, Swiss Fed Inst Technol, Funct Genom Ctr, CH-8057 Zurich, Switzerland
[3] Univ Zurich, Inst Mol Biol, CH-8057 Zurich, Switzerland
[4] Inst Mol Syst Biol, Zurich, Switzerland
[5] Univ Zurich, Fac Sci, CH-8057 Zurich, Switzerland
关键词
proteomics; mass spectrometry; proteome catalog; targeted quantitative proteomics; proteotypic peptide (PTP); multiple reaction monitoring (MRM); technology development; analysis-driven experimentation (ADE); systems biology;
D O I
10.4161/fly.4532
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
Proteomic analyses are critically important for systems biology because important aspects related to the structure, function and control of biological systems are only amenable by direct protein measurements. It has become apparent that the current proteomics technologies are unlikely to allow routine, quantitative measurements of whole proteomes. We have therefore suggested and largely implemented a two-step strategy for quantitative proteome analysis. In a first step, the discovery phase, the proteome observable by mass spectrometry is extensively analyzed. The resulting proteome catalog can then be used to select peptides specific to only one protein, so-called proteotypic peptides (PTPs). It represents the basis to realize sensitive, robust and reproducible measurements based on targeted mass spectrometry of these PTPs in a subsequent scoring phase. In this Extra View we describe the need for such proteome catalogs and their multiple benefits for catalyzing the shift towards targeted quantitative proteomic analysis and beyond. We use the Insulin signaling cascade as a representative example to illustrate the limitations of currently used proteomics approaches for the specific analysis of individual pathway components, and describe how the recently published Drosophila proteome catalog already helped to overcome many of these limitations.
引用
收藏
页码:182 / 186
页数:5
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