Enhanced identification of peptides lacking basic residues by LC-ESI-MS/MS analysis of singly charged peptides

Proteomics. 2012 May;12(9):1303-9. doi: 10.1002/pmic.201100569.

Abstract

Peptide sequences lacking basic residues (arginine, lysine, or histidine, referred to as "base-less") are of particular importance in proteomic experiments targeting protein C-termini or employing nontryptic proteases such as GluC or chymotrypsin. We demonstrate enhanced identification of base-less peptides by focused analysis of singly charged precursors in liquid chromatography (LC) electrospray ionization (ESI) tandem mass spectrometry (MS/MS). Singly charged precursors are often excluded from fragmentation and sequence analysis in LC-MS/MS. We generated different pools of base-less and base-containing peptides by tryptic and nontryptic digestion of bacterial proteomes. Focused LC-MS/MS analysis of singly charged precursor ions yielded predominantly base-less peptide identifications. Similar numbers of base-less peptides were identified by LC-MS/M Sanalysis targeting multiply charged precursors. There was little redundancy between the base-less sequences derived by both MS/MS schemes. In the present experimental outcome, additional LC-MS/MS analysis of singly charged precursors substantially increased the identification rate of base-less sequences derived from multiply charged precursors. In conclusion, LC-MS/MS based identification of base-less peptides is substantially enhanced by additional focused analysis of singly charged precursors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Chromatography, Liquid / methods*
  • Escherichia coli Proteins / analysis
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / metabolism
  • Molecular Sequence Data
  • Peptide Fragments / analysis
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • Proteomics / methods*
  • Serine Proteases / metabolism
  • Spectrometry, Mass, Electrospray Ionization / methods*
  • Tandem Mass Spectrometry / methods

Substances

  • Escherichia coli Proteins
  • Peptide Fragments
  • Serine Proteases