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PMID: 21472614 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Improving proteome coverage on a LTQ-Orbitrap using design of experiments.

Journal of the American Society for Mass Spectrometry ·Vol. 22 ·No. 4 ·2011-04-00 ·Pages 773-83

Andrews GL, Dean RA, Hawkridge AM, Muddiman DC

Abstract

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.

MeSH Terms
Peptide Fragments Peptide Mapping Proteome/chemistry Proteomics/methods Research Design Saccharomyces cerevisiae Proteins/chemistry Tandem Mass Spectrometry/methods Temperature
Chemicals
Peptide Fragments Proteome Saccharomyces cerevisiae Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Andrews Genna L
W. M. Keck FT-ICR Mass Spectrometry Laboratory, Department of Chemistry, North Carolina State University, Raleigh, NC 27695, USA.
Dean Ralph A
Hawkridge Adam M
Muddiman David C
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Article Info
Journal
Journal of the American Society for Mass Spectrometry
Abbr.
J Am Soc Mass Spectrom
ISSN
1879-1123
Published
2011-04-00
Epub
2011-00-15
Pages
773-83
Language
English
Region
United States
NLM ID
9010412
PMCID
PMC3145359
Subset
IM
Grants
NIGMS NIH HHS · T32 GM008776-08 · United States
NCI NIH HHS · K25 CA128666-04 · United States
NIGMS NIH HHS · T32 GM008776 · United States
NCI NIH HHS · K25 CA128666 · United States
NIGMS NIH HHS · 5T32GM00-8776-08 · United States
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