Review of software tools for design and analysis of large scale MRM proteomic datasets

Methods. 2013 Jun 15;61(3):287-98. doi: 10.1016/j.ymeth.2013.05.004. Epub 2013 May 21.

Abstract

Selective or Multiple Reaction monitoring (SRM/MRM) is a liquid-chromatography (LC)/tandem-mass spectrometry (MS/MS) method that enables the quantitation of specific proteins in a sample by analyzing precursor ions and the fragment ions of their selected tryptic peptides. Instrumentation software has advanced to the point that thousands of transitions (pairs of primary and secondary m/z values) can be measured in a triple quadrupole instrument coupled to an LC, by a well-designed scheduling and selection of m/z windows. The design of a good MRM assay relies on the availability of peptide spectra from previous discovery-phase LC-MS/MS studies. The tedious aspect of manually developing and processing MRM assays involving thousands of transitions has spurred to development of software tools to automate this process. Software packages have been developed for project management, assay development, assay validation, data export, peak integration, quality assessment, and biostatistical analysis. No single tool provides a complete end-to-end solution, thus this article reviews the current state and discusses future directions of these software tools in order to enable researchers to combine these tools for a comprehensive targeted proteomics workflow.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Chromatography, Liquid / methods
  • Chromatography, Liquid / standards
  • Chromatography, Liquid / statistics & numerical data*
  • Humans
  • Ions
  • Peptide Fragments / analysis*
  • Proteins / analysis*
  • Proteomics / methods
  • Proteomics / standards
  • Proteomics / statistics & numerical data*
  • Software*
  • Tandem Mass Spectrometry / methods
  • Tandem Mass Spectrometry / standards
  • Tandem Mass Spectrometry / statistics & numerical data*

Substances

  • Ions
  • Peptide Fragments
  • Proteins