Peptides derivatized with bicyclic quaternary ammonium ionization tags. Sequencing via tandem mass spectrometry

Bartosz Setner, Magdalena Rudowska, Ewelina Klem, Marek Cebrat, Zbigniew Szewczuk

Research output: Contribution to journalArticle

Abstract

Improving the sensitivity of detection and fragmentation of peptides to provide reliable sequencing of peptides is an important goal of mass spectrometric analysis. Peptides derivatized by bicyclic quaternary ammonium ionization tags: 1-azabicyclo[2.2.2]octane (ABCO) or 1,4-diazabicyclo[2.2.2]octane (DABCO), are characterized by an increased detection sensitivity in electrospray ionization mass spectrometry (ESI-MS) and longer retention times on the reverse-phase (RP) chromatography columns. The improvement of the detection limit was observed even for peptides dissolved in 10 mM NaCl. Collision-induced dissociation tandem mass spectrometry of quaternary ammonium salts derivatives of peptides showed dominant a- and b-type ions, allowing facile sequencing of peptides. The bicyclic ionization tags are stable in collision-induced dissociation experiments, and the resulted fragmentation pattern is not significantly influenced by either acidic or basic amino acid residues in the peptide sequence. Obtained results indicate the general usefulness of the bicyclic quaternary ammonium ionization tags for ESI-MS/MS sequencing of peptides.

Original languageEnglish (US)
Pages (from-to)995-1001
Number of pages7
JournalJournal of Mass Spectrometry
Volume49
Issue number10
DOIs
StatePublished - Oct 1 2014
Externally publishedYes

Keywords

  • ABCO
  • DABCO
  • derivatization of peptides
  • peptide sequencing

ASJC Scopus subject areas

  • Spectroscopy
  • Medicine(all)

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