Publication | Open Access
Sequencing-Grade <i>De novo</i> Analysis of MS/MS Triplets (CID/HCD/ETD) From Overlapping Peptides
70
Citations
32
References
2013
Year
Molecular BiologyPeptide ScienceAssembled Tandem MassFull-length DeProteomic TechnologyProtein FoldingProteomicsBiochemistryBioinformaticsProtein BioinformaticsMs/ms TripletsNatural SciencesPeptide LibraryMass SpectrometryProtein Mass SpectrometrySystems BiologyMedicinePeptides YieldMolecular Fragmentation
Full-length de novo sequencing of unknown proteins remains a challenging open problem. Traditional methods that sequence spectra individually are limited by short peptide length, incomplete peptide fragmentation, and ambiguous de novo interpretations. We address these issues by determining consensus sequences for assembled tandem mass (MS/MS) spectra from overlapping peptides (e.g., by using multiple enzymatic digests). We have combined electron-transfer dissociation (ETD) with collision-induced dissociation (CID) and higher-energy collision-induced dissociation (HCD) fragmentation methods to boost interpretation of long, highly charged peptides and take advantage of corroborating b/y/c/z ions in CID/HCD/ETD. Using these strategies, we show that triplet CID/HCD/ETD MS/MS spectra from overlapping peptides yield de novo sequences of average length 70 AA and as long as 200 AA at up to 99% sequencing accuracy.
| Year | Citations | |
|---|---|---|
Page 1
Page 1