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Analysis of the trypanosome flagellar proteome using a combined electron transfer collisionally activated dissociation strategy.

Research output: Contribution to journalJournal articlepeer-review

  • Sarah R. Hart
  • King Wai Wai Lau
  • Zhiqi Hao
  • Richard Broadhead
  • Neil Portman
  • Andreas Huhmer
  • Keith Gull
  • Paul G. McKean
  • Simon J. Hubbard
  • Simon J. Gaskell
<mark>Journal publication date</mark>02/2009
<mark>Journal</mark>Journal of The American Society for Mass Spectrometry
Issue number2
Number of pages9
Pages (from-to)167-175
Publication StatusPublished
<mark>Original language</mark>English


The use of electron-transfer dissociation as an alternative peptide ion activation method for generation of protein sequence information is examined here in comparison with the conventional method of choice, collisionally activated dissociation, using a linear ion trapping instrument. Direct comparability between collisionally and electron-transfer-activated product ion data were ensured by employing an activation-switching method during acquisition, sequentially activating precisely the same precursor ion species with each fragmentation method in turn. Sequest (Thermo Fisher Scientific, San Jose, CA) searching of product ion data generated an overlapping yet distinct pool of polypeptide identifications from the products of collisional and electron-transfer-mediated activation products. To provide a highly confident set of protein recognitions, identification data were filtered using parameters that achieved a peptide false discovery rate of 1%, with two or more independent peptide assignments required for each protein. The use of electron transfer dissociation (ETD) has allowed us to identify additional peptides where the quality of product ion data generated by collisionally activated dissociation (CAD) was insufficient to infer peptide sequence. Thus, a combined ETD/CAD approach leads to the recognition of more peptides and proteins than are achieved using peptide analysis by CAD- or ETD-based tandem mass spectrometry alone.