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J Am Soc Mass Spectrom. 2011 Aug;22(8):1373-80. doi: 10.1007/s13361-011-0142-8. Epub 2011 Apr 22.

Software lock mass by two-dimensional minimization of peptide mass errors.

Author information

1
Proteomics and Signal Transduction, Max-Planck Institute of Biochemistry, Martinsried, Germany. cox@biochem.mpg.de

Abstract

Mass accuracy is a key parameter in proteomic experiments, improving specificity, and success rates of peptide identification. Advances in instrumentation now make it possible to routinely obtain high resolution data in proteomic experiments. To compensate for drifts in instrument calibration, a compound of known mass is often employed. This 'lock mass' provides an internal mass standard in every spectrum. Here we take advantage of the complexity of typical peptide mixtures in proteomics to eliminate the requirement for a physical lock mass. We find that mass scale drift is primarily a function of the m/z and the elution time dimensions. Using a subset of high confidence peptide identifications from a first pass database search, which effectively substitute for the lock mass, we set up a global mathematical minimization problem. We perform a simultaneous fit in two dimensions using a function whose parameterization is automatically adjusted to the complexity of the analyzed peptide mixture. Mass deviation of the high confidence peptides from their calculated values is then minimized globally as a function of both m/z value and elution time. The resulting recalibration function performs equal or better than adding a lock mass from laboratory air to LTQ-Orbitrap spectra. This 'software lock mass' drastically improves mass accuracy compared with mass measurement without lock mass (up to 10-fold), with none of the experimental cost of a physical lock mass, and it integrated into the freely available MaxQuant analysis pipeline ( www.maxquant.org ).

PMID:
21953191
PMCID:
PMC3231580
DOI:
10.1007/s13361-011-0142-8
[Indexed for MEDLINE]
Free PMC Article

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