Comparison of collisionally activated dissociation mass spectra for the identification of cyclopeptides and cyclodepsipeptides
β Scribed by F. Cavelier; C. Enjalbal; J. Martinez; M. Roque; P. Sanchez; J.-L. Aubagnac
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 81 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0951-4198
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β¦ Synopsis
Collisionally activated dissociation (CAD) spectra of protonated molecules of cyclopeptides and cyclodepsipeptides obtained with two different mass spectrometry systems were compared. Fragmentations were obtained either from collisions induced in the ion source of an electrospray mass spectrometer fitted with a single quadrupole by increasing the extracting cone voltage or from collisions with an inert gas in a free-field area of a fast-atom bombardment (FAB) mass spectrometer. Similar fragmentation pathways were produced with the two configurations even though actual tandem mass spectrometry experiments with magnetic and electric sectors provided more information than cone-induced dissociations. However, only the latter mode allowed us to perform mass spectrometric analyses coupled to liquid chromatography (LC/ ESI-MS) at low cost on commercially widespread instruments.
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The collision-induced tandem mass spectral data for MH' and [M -HI-ions from six bio-active peptides from Litoriu rubella are compared. Backbone cleavages of [M -HI-ions provide sequencing information for five of the peptides [e.g. Phe Pro 'lkp Leu (NH,) and pGlu Phe Pro 'lkp Leu (NH,)] and in these
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