A high-quality catalog of the Drosophila melanogaster proteome

被引:219
作者
Brunner, Erich
Ahrens, Christian H.
Mohanty, Sonali
Baetschmann, Hansruedi
Loevenich, Sandra
Potthast, Frank
Deutsch, Eric W.
Panse, Christian
de Lichtenberg, Ulrik
Rinner, Oliver
Lee, Hookeun
Pedrioli, Patrick G. A.
Malmstrom, Johan
Koehler, Katja
Schrimpf, Sabine
Krijgsveld, Jeroen
Kregenow, Floyd
Heck, Albert J. R.
Hafen, Ernst
Schlapbach, Ralph
Aebersold, Ruedi
机构
[1] ETH Honggerberg, Inst Mol Syst Biol, Swiss Fed Inst Technol, CH-8093 Zurich, Switzerland
[2] Univ Zurich, Ctr Model Organism Proteomes, CH-8057 Zurich, Switzerland
[3] ETH, Funct Genom Ctr, CH-8057 Zurich, Switzerland
[4] Inst Syst Biol, Seattle, WA 98103 USA
[5] Tech Univ Denmark, Ctr Biol Sequence Anal, Biocentrum, DK-2800 Lyngby, Denmark
[6] Leo Pharmaceut Prod, DK-2750 Ballerup, Denmark
[7] Univ Zurich, Inst Mol Biol, CH-8057 Zurich, Switzerland
[8] Univ Utrecht, Dept Biomol Mass Spectrometry, Bijvoet Ctr Biomol Res, NL-3584 CA Utrecht, Netherlands
[9] Univ Utrecht, Inst Pharmaceut Sci, NL-3584 CA Utrecht, Netherlands
[10] Univ Zurich, Fac Sci, CH-8057 Zurich, Switzerland
关键词
D O I
10.1038/nbt1300
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Understanding how proteins and their complex interaction networks convert the genomic information into a dynamic living organism is a fundamental challenge in biological sciences. As an important step towards understanding the systems biology of a complex eukaryote, we cataloged 63% of the predicted Drosophila melanogaster proteome by detecting 9,124 proteins from 498,000 redundant and 72,281 distinct peptide identifications. This unprecedented high proteome coverage for a complex eukaryote was achieved by combining sample diversity, multidimensional biochemical fractionation and analysis-driven experimentation feedback loops, whereby data collection is guided by statistical analysis of prior data. We show that high-quality proteomics data provide crucial information to amend genome annotation and to confirm many predicted gene models. We also present experimentally identified proteotypic peptides matching similar to 50% of D. melanogaster gene models. This library of proteotypic peptides should enable fast, targeted and quantitative proteomic studies to elucidate the systems biology of this model organism.
引用
收藏
页码:576 / 583
页数:8
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