Abstract
We report an automated method for determining charge states from high-resolution mass spectra. Fourier transforms of isotope packets from high-resolution mass spectra are compared to Fourier transforms of modeled isotopic peak packets for a range of charge states. The charge state for the experimental ion packet is determined by the model isotope packet that yields the best match in the comparison of the Fourier transforms. This strategy is demonstrated for determining peptide ion charge states from "zoom scan" data from a linear quadrupole ion trap mass spectrometer, enabling the subsequent automated identification of singly- through quadruply-charged peptide ions, while reducing the numbers of conflicting identifications from ambiguous charge state assignments. We also apply this technique to determine the charges of intact protein ions from LC-FTICR data, demonstrating that it is more sensitive under these experimental conditions than two existing algorithms. The strategy outlined in this paper should be generally applicable to mass spectra obtained from any instrument capable of isotopic resolution.
Original language | English |
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Pages (from-to) | 903-915 |
Number of pages | 13 |
Journal | Journal of the American Society for Mass Spectrometry |
Volume | 17 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2006 |
Funding
The authors acknowledge Hayes McDonald for advice on high-resolution measurements in quadrupole ion trap mass spectrometers. Research was funded by the United States Department of Energy’s Office of Biological and Environmental Research through the Genomics: GTL Center for Molecular and Cellular Systems. Oak Ridge National Laboratory is managed by UT-Battelle, LLC for the U.S. Department of Energy under contract number DE-AC05-00OR22725.
Funders | Funder number |
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GTL Center for Molecular and Cellular Systems | |
U.S. Department of Energy | DE-AC05-00OR22725 |
Biological and Environmental Research | |
Oak Ridge National Laboratory |