Document Type
Article
Publication Date
6-1-2006
Abstract
Most MALDI instrumentation uses UV lasers. We have designed a MALDI-IM-oTOF-MS which employs both a Nd:YAG laser pumped optical parametric oscillator OPOTEK, λ = 2.8-3.2 μm at 20 Hz) to perform IR-LDI or IR-MALDI and a Nd:YLF laser (Crystalaser, λ = 249 nm at 200 Hz) for the UV. Ion mobility (IM) gives a fast separation and analysis of biomolecules from complex mixtures in which ions of similar chemical type fall along well-defined "trend lines". Our data shows that ion mobility allows multiply charged monomers and multimers to be resolved; thus, yielding pure spectra of the singly charged protein ion which are virtually devoid of chemical noise. In addition, we have demonstrated that IR-LDI produced similar results as IR-MALDI for the direct tissue analysis of phospholipids from rat brain. © 2006 American Chemical Society.
Publication Source (Journal or Book title)
Journal of Proteome Research
First Page
1484
Last Page
1487
Recommended Citation
Woods, A., Ugarov, M., Jackson, S., Egan, T., Wang, H., Murray, K., & Schultz, J. (2006). IR-MALDI-LDI combined with ion mobility orthogonal time-of-flight mass spectrometry. Journal of Proteome Research, 5 (6), 1484-1487. https://doi.org/10.1021/pr060055l