IR-MALDI-LDI combined with ion mobility orthogonal time-of-flight mass spectrometry
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
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