4.8 Article

Toward Full Peptide Sequence Coverage by Dual Fragmentation Combining Electron-Transfer and Higher-Energy Collision Dissociation Tandem Mass Spectrometry

Journal

ANALYTICAL CHEMISTRY
Volume 84, Issue 22, Pages 9668-9673

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac3025366

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Funding

  1. Netherlands Proteomics Center
  2. PRIME-XS project [262067]
  3. European Union
  4. Netherlands Organization for Scientific Research (NWO) [700.10.429]

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Increasing peptide sequence coverage by tandem mass spectrometry improves confidence in database search-based peptide identification and facilitates mapping of post-translational modifications and de novo sequencing. Inducing 2-fold fragmentation by combining electron-transfer and higher-energy collision dissociation (EThcD) generates dual fragment ion series and facilitates extensive peptide backbone fragmentation. After an initial electron-transfer dissociation step, all ions including the unreacted precursor ions are subjected to collision induced dissociation which yields b/y- and c/z-type fragment ions in a single spectrum. This new fragmentation scheme provides richer spectra and substantially increases the peptide sequence coverage and confidence in peptide identification.

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