| Literature DB >> 16740000 |
Amina S Woods1, Michael Ugarov, Shelley N Jackson, Thomas Egan, Hay-Yan J Wang, Kermit K Murray, J Albert Schultz.
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, lambda = 2.8-3.2 microm at 20 Hz) to perform IR-LDI or IR-MALDI and a Nd:YLF laser (Crystalaser, lambda = 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.Entities:
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Year: 2006 PMID: 16740000 PMCID: PMC2953763 DOI: 10.1021/pr060055l
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466