The One Hour Yeast Proteome

Alexander S. Hebert(University of Wisconsin–Madison), Alicia Richards(University of Wisconsin–Madison), Derek J. Bailey(University of Wisconsin–Madison), Arne Ulbrich(University of Wisconsin–Madison), Emma E. Coughlin(University of Wisconsin–Madison), Michael S. Westphall(University of Wisconsin–Madison), Joshua J. Coon(University of Wisconsin–Madison)
Molecular & Cellular Proteomics
October 19, 2013
Cited by 555Open Access
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Abstract

We describe the comprehensive analysis of the yeast proteome in just over one hour of optimized analysis. We achieve this expedited proteome characterization with improved sample preparation, chromatographic separations, and by using a new Orbitrap hybrid mass spectrometer equipped with a mass filter, a collision cell, a high-field Orbitrap analyzer, and, finally, a dual cell linear ion trap analyzer (Q-OT-qIT, Orbitrap Fusion). This system offers high MS(2) acquisition speed of 20 Hz and detects up to 19 peptide sequences within a single second of operation. Over a 1.3 h chromatographic method, the Q-OT-qIT hybrid collected an average of 13,447 MS(1) and 80,460 MS(2) scans (per run) to produce 43,400 (x) peptide spectral matches and 34,255 (x) peptides with unique amino acid sequences (1% false discovery rate (FDR)). On average, each one hour analysis achieved detection of 3,977 proteins (1% FDR). We conclude that further improvements in mass spectrometer scan rate could render comprehensive analysis of the human proteome within a few hours.


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