Investigation of c ions formed by N-terminally charged peptides upon collision-induced dissociation

J Mass Spectrom. 2016 Nov;51(11):989-997. doi: 10.1002/jms.3841.

Abstract

Peptide fragments such as b and y sequence ions generated upon low-energy collision-induced dissociation have been routinely used for tandem mass spectrometry (MS/MS)-based peptide/protein identification. The underlying formation mechanisms have been studied extensively and described within the literature. As a result, the 'mobile proton model' and 'pathways in competition model' have been built to interpret a majority of peptide fragmentation behavior. However, unusual peptide fragments which involve unfamiliar fragmentation pathways or various rearrangement reactions occasionally appear in MS/MS spectra, resulting in confused MS/MS interpretations. In this work, a series of unfamiliar c ions are detected in MS/MS spectra of the model peptides having an N-terminal Arg or deuterohemin group upon low-energy collision-induced dissociation process. Both the protonated Arg and deuterohemin group play an important role in retention of a positive charge at the N-terminus that is remote from the cleavage sites. According to previous reports and our studies involving amino acid substitutions and hydrogen-deuterium exchange, we propose a McLafferty-type rearrangement via charge-remote fragmentation as the potential mechanism to explain the formation of c ions from precursor peptide ions or unconventional b ions. Density functional theory calculations are also employed in order to elucidate the proposed fragmentation mechanisms. Copyright © 2016 John Wiley & Sons, Ltd.

Keywords: McLafferty-type rearrangement; c ions; charge-remote; fixed-charge; peptide fragmentation.

MeSH terms

  • Amino Acid Sequence
  • Deuterium
  • Ions / chemistry
  • Peptide Fragments / chemistry
  • Peptides / chemistry*
  • Protons
  • Tandem Mass Spectrometry

Substances

  • Ions
  • Peptide Fragments
  • Peptides
  • Protons
  • Deuterium