Do collisions inside the collision cell play a relevant role in CID‐LIFT experiments?
- 8 December 2006
- journal article
- research article
- Published by Wiley in Journal of Mass Spectrometry
- Vol. 42 (1) , 117-126
Abstract
Collision experiments are a valid approach to characterize the ionic species generated by matrix assisted laser desorption ionization (MALDI). When a time‐of‐flight analyzer is employed, three different approaches are available for these experiments: the postsource decay (PSD), the LIFT and the MALDI‐TOF/TOF. The last two are of particular interest because of the overcoming of the PSD problems related to mass calibration of the product ion spectra.Experiments performed by LIFT on linear or cyclic peptides, in presence or in absence of collision gas in the collision cell, gave evidence of an unexpected behavior: the two spectra were practically superimposable, and in the former case only a few new fragmentation channels were activated with low yield. These results mean that the selected ion exhibits a large amount of internal energy, capable of promoting fragmentation processes in the time window corresponding to the flight time between ion source and the acceleration electrode placed after the collision cell.Experiments performed by varying the plume density show that this internal energy uptake occurs in the expanding plume, through multiple collisions. The LIFT data have been compared with those achieved by collisions of ESI‐generated [MH]+ ions of angotensin II performed under ‘in‐source’ conditions and by triple‐quadrupole experiments. The obtained results show a strong similarity among the spectra, indicating that the internal energy uptake in a MALDI source is comparable with that of 40‐eV ions colliding with Ar in a triple‐quadrupole instrument. Copyright © 2006 John Wiley & Sons, Ltd.Keywords
This publication has 9 references indexed in Scilit:
- Internal energies of analyte ions generated from different matrix-assisted laser desorption/ionization matricesJournal of Mass Spectrometry, 2000
- The initial ion velocity and its dependence on matrix, analyte and preparation method in ultraviolet matrix-assisted laser desorption/ionizationJournal of Mass Spectrometry, 1999
- Post-source decay analysis in matrix-assisted laser desorption/ionization mass spectrometry of biomoleculesJournal of Mass Spectrometry, 1997
- Photochemical Versus Thermal Mechanisms in Matrix-assisted Laser Desorption/Ionization Probed by Back Side DesorptionRapid Communications in Mass Spectrometry, 1996
- Mass spectrometric sequencing of linear peptides by product‐ion analysis in a reflectron time‐of‐flight mass spectrometer using matrix‐assisted laser desorption ionizationRapid Communications in Mass Spectrometry, 1993
- Fundamental aspects of postsource decay in matrix-assisted laser desorption mass spectrometry. 1. Residual gas effectsThe Journal of Physical Chemistry, 1992
- Measurement of initial translational energies of peptide ions in laser desorption/ionization mass spectrometryJournal of Mass Spectrometry, 1992
- Ultraviolet laser ablation of organic polymersChemical Reviews, 1989
- New method for metastable ion studies with a time of flight mass spectrometer. Future application to molecular structure determinationsAnalytical Chemistry, 1985