4.7 Article

Using Power Spectrum Analysis to Evaluate 18O-Water Labeling Data Acquired from Low Resolution Mass Spectrometers

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 9, Issue 8, Pages 4306-4312

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/pr100642q

Keywords

power spectral analysis; low-pass and band filtering; correlation of filtered spectrum with a theoretical isotope distribution; mass spectrometry; quantification; ratio estimation; O-18-water labeling; bioinformatics

Funding

  1. NIAID [HHSN272200800048C]
  2. McCoy Foundation
  3. Juvenile Diabetes Research Foundation

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We describe a method for ratio estimations in O-18-water labeling experiments acquired from low resolution isotopically resolved data. The method is implemented in a software package specifically designed for use in experiments making use of zoom-scan mode data acquisition. Zoom-scan mode data allow commonly used ion trap mass spectrometers to attain isotopic resolution, which makes them amenable to use in labeling schemes such as O-18-water labeling, but algorithms and software developed for high resolution instruments may not be appropriate for the lower resolution data acquired in zoom-scan mode. The use of power spectrum analysis is proposed as a general approach that may be uniquely suited to these data types. The software implementation uses a power spectrum to remove high-frequency noise and band-filter contributions from coeluting species of differing charge states. From the elemental composition of a peptide sequence, we generate theoretical isotope envelopes of heavy-light peptide pairs in five different ratios; these theoretical envelopes are correlated with the filtered experimental zoom scans. To automate peptide quantification in high-throughput experiments, we have implemented our approach in a computer program, MassXplorer. We demonstrate the application of MassXplorer to two model mixtures of known proteins and to a complex mixture of mouse kidney cortical extract. Comparison with another algorithm for ratio estimations demonstrates the increased precision and automation of MassXplorer.

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