In most MALDI peptide profiling cases, sequencing is required to identify peptides of interest, preferentially by using different mass spectrometry techniques. Using identical samples, we determined the number of false positive matches in sequence of peptide identification using different mass spectrometers. This paper demonstrates that the reliability of the identification phase greatly benefits from concerted MS-technologies and determines the influence of mass accuracy, signal-to-noise and statistical score on peptide identification.

ESI-orbitrap, False positive match in sequence, MALDI-FT-ICR, MALDI-TOF/TOF, Peptide identification
dx.doi.org/10.1021/pr800489a, hdl.handle.net/1765/32509
Journal of Proteome Research
Erasmus MC: University Medical Center Rotterdam

Stoop, M.P, Lamers, R.J.A.N, Burgers, P.C, Smitt, P.A, Hintzen, R.Q, & Luider, T.M. (2008). The rate of false positive sequence matches of peptides profiled by MALDI MS and identified by MS/MS. Journal of Proteome Research, 7(11), 4841–4847. doi:10.1021/pr800489a