One-hour proteome analysis in yeast

被引:88
|
作者
Richards, Alicia L. [1 ,2 ]
Hebert, Alexander S. [1 ,3 ]
Ulbrich, Arne [1 ,2 ]
Bailey, Derek J. [1 ,2 ]
Coughlin, Emma E. [1 ]
Westphall, Michael S. [1 ]
Coon, Joshua J. [1 ,2 ,3 ]
机构
[1] Univ Wisconsin, Genome Ctr Wisconsin, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[3] Univ Wisconsin, Biomol Chem, Madison, WI USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
PEPTIDE IDENTIFICATION;
D O I
10.1038/nprot.2015.040
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent advances in chromatography and mass spectrometry (MS) have made rapid and deep proteomic profiling possible. To maximize the performance of the recently produced Orbitrap hybrid mass spectrometer, we have developed a protocol that combines improved sample preparation (including optimized cellular lysis by extensive bead beating) and chromatographic conditions (specifically, 30-cm capillary columns packed with 1.7-mm bridged ethylene hybrid material) and the manufacture of a column heater (to accommodate flow rates of 350-375 nl/min) that increases the number of proteins identified across a single liquid chromatography-tandem MS (LC-MS/MS) separation, thereby reducing the need for extensive sample fractionation. This strategy allowed the identification of up to 4,002 proteins (at a 1% false discovery rate (FDR)) in yeast (Saccharomyces cerevisiae strain BY4741) over 70 min of LC-MS/MS analysis. Quintuplicate analysis of technical replicates reveals 83% overlap at the protein level, thus demonstrating the reproducibility of this procedure. This protocol, which includes cell lysis, overnight tryptic digestion, sample analysis and database searching, takes similar to 24 h to complete. Aspects of this protocol, including chromatographic separation and instrument parameters, can be adapted for the optimal analysis of other organisms.
引用
收藏
页码:701 / 714
页数:14
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