An assessment of current bioinformatic solutions for analyzing LC-MS data acquired by selected reaction monitoring technology

Proteomics. 2012 Apr;12(8):1176-84. doi: 10.1002/pmic.201100571.

Abstract

Selected reaction monitoring (SRM) is an accurate quantitative technique, typically used for small-molecule mass spectrometry (MS). SRM has emerged as an important technique for targeted and hypothesis-driven proteomic research, and is becoming the reference method for protein quantification in complex biological samples. SRM offers high selectivity, a lower limit of detection and improved reproducibility, compared to conventional shot-gun-based tandem MS (LC-MS/MS) methods. Unlike LC-MS/MS, which requires computationally intensive informatic postanalysis, SRM requires preacquisition bioinformatic analysis to determine proteotypic peptides and optimal transitions to uniquely identify and to accurately quantitate proteins of interest. Extensive arrays of bioinformatics software tools, both web-based and stand-alone, have been published to assist researchers to determine optimal peptides and transition sets. The transitions are oftentimes selected based on preferred precursor charge state, peptide molecular weight, hydrophobicity, fragmentation pattern at a given collision energy (CE), and instrumentation chosen. Validation of the selected transitions for each peptide is critical since peptide performance varies depending on the mass spectrometer used. In this review, we provide an overview of open source and commercial bioinformatic tools for analyzing LC-MS data acquired by SRM.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Algorithms
  • Chromatography, Liquid / methods*
  • Chromatography, Liquid / standards
  • Computational Biology / methods*
  • Computational Biology / standards
  • Databases, Protein
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Internet
  • Molecular Weight
  • Peptides / analysis*
  • Proteolysis
  • Reproducibility of Results
  • Saccharomyces cerevisiae / chemistry
  • Sensitivity and Specificity
  • Software*
  • Tandem Mass Spectrometry / methods*
  • Tandem Mass Spectrometry / standards

Substances

  • Peptides