Improving Proteome Coverage on a LTQ-Orbitrap Using Design of Experiments

被引:51
作者
Andrews, Genna L. [1 ]
Dean, Ralph A. [2 ]
Hawkridge, Adam M. [1 ]
Muddiman, David C. [1 ]
机构
[1] N Carolina State Univ, Dept Chem, WM Keck FT ICR Mass Spectrometry Lab, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Ctr Integrated Fungal Res, Raleigh, NC 27695 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
LTQ-Orbitrap XL MS/MS instrument parameters; Design of experiments; Fractional-factorial design; Saccharomyces cerevisiae; Proteomics; MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; STATISTICAL-MODEL; MESSENGER-RNA; PEAK-CAPACITY; ESI-MS; IDENTIFICATION; PROTEINS; PARAMETERS; ABUNDANCE;
D O I
10.1007/s13361-011-0075-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Design of experiments (DOE) was used to determine improved settings for a LTQ-Orbitrap XL to maximize proteome coverage of Saccharomyces cerevisiae. A total of nine instrument parameters were evaluated with the best values affording an increase of approximately 60% in proteome coverage. Utilizing JMP software, 2 DOE screening design tables were generated and used to specify parameter values for instrument methods. DOE 1, a fractional factorial design, required 32 methods fully resolving the investigation of six instrument parameters involving only half the time necessary for a full factorial design of the same resolution. It was advantageous to complete a full factorial design for the analysis of three additional instrument parameters. Measured with a maximum of 1% false discovery rate, protein groups, unique peptides, and spectral counts gauged instrument performance. Randomized triplicate nanoLC-LTQ-Orbitrap XL MS/MS analysis of the S. cerevisiae digest demonstrated that the following five parameters significantly influenced proteome coverage of the sample: (1) maximum ion trap ionization time; (2) monoisotopic precursor selection; (3) number of MS/MS events; (4) capillary temperature; and (5) tube lens voltage. Minimal influence on the proteome coverage was observed for the remaining four parameters (dynamic exclusion duration, resolving power, minimum count threshold to trigger a MS/MS event, and normalized collision energy). The DOE approach represents a time- and cost-effective method for empirically optimizing MS-based proteomics workflows including sample preparation, LC conditions, and multiple instrument platforms.
引用
收藏
页码:773 / 783
页数:11
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