Precision enhancement of MALDI-TOF MS using high resolution peak detection and label-free alignment

We have developed an automated procedure for aligning peaks in multiple TOF spectra that eliminates common timing errors and small variations in spectrometer output. Our method incorporates high-resolution peak detection, re-binning, and robust linear data fitting in the time domain. This procedure...

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Published inProteomics (Weinheim) Vol. 8; no. 8; pp. 1530 - 1538
Main Authors Tracy, Maureen B, Chen, Haijian, Weaver, Dennis M, Malyarenko, Dariya I, Sasinowski, Maciek, Cazares, Lisa H, Drake, Richard R, Semmes, O. John, Tracy, Eugene R, Cooke, William E
Format Journal Article
LanguageEnglish
Published Weinheim Wiley-VCH Verlag 01.04.2008
WILEY-VCH Verlag
WILEY‐VCH Verlag
Wiley-VCH
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ISSN1615-9853
1615-9861
1615-9861
DOI10.1002/pmic.200701146

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Summary:We have developed an automated procedure for aligning peaks in multiple TOF spectra that eliminates common timing errors and small variations in spectrometer output. Our method incorporates high-resolution peak detection, re-binning, and robust linear data fitting in the time domain. This procedure aligns label-free (uncalibrated) peaks to minimize the variation in each peak's location from one spectrum to the next, while maintaining a high number of degrees of freedom. We apply our method to replicate pooled-serum spectra from multiple laboratories and increase peak precision (t/σt) to values limited only by small random errors (with σt less than one time count in 89 out of 91 instances, 13 peaks in seven datasets). The resulting high precision allowed for an order of magnitude improvement in peak m/z reproducibility. We show that the CV for m/z is 0.01% (100 ppm) for 12 out of the 13 peaks that were observed in all datasets between 2995 and 9297 Da.
Bibliography:http://dx.doi.org/10.1002/pmic.200701146
National Cancer Institute - No. CA101479; No. CA126118; No. CA085067
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ISSN:1615-9853
1615-9861
1615-9861
DOI:10.1002/pmic.200701146