Abstract
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is an established technique for the analysis of biological macromolecules. Its relative insensitivity to pollutants makes MALDI-MS very suitable for the direct analysis of biological samples. As such, it has facilitated great advances in the field of biomolecular imaging mass spectrometry. Traditionally, MALDI-MS imaging is performed in a scanning microprobe methodology. However, in a recent study we have demonstrated an alternative methodology; the so-called microscope mode, where the requirement for a highly focused ionization beam is removed. Spatial details from within the desorption area are conserved during the flight of the ions through the mass analyzer, and a magnified ion image is projected onto a 2D-detector. In this paper, we demonstrate how imaging mass spectrometry benefits from the microscope mode approach. For the first time, high-lateral resolution ion images were recorded using infrared MALDI at 2.94 μm wavelength. The ion optical resolution achieved was well below the theoretical limit of (light-) diffraction for the setup used, which is impossible to achieve in the conventional scanning microprobe approach.
| Original language | English |
|---|---|
| Pages (from-to) | 671-673 |
| Number of pages | 3 |
| Journal | Journal of Proteome Research |
| Volume | 4 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - May 2005 |
| Externally published | Yes |
Keywords
- Imaging mass spectrometry
- IR-MALDI
- Microscope mode
- Stigmatic ion optics
- Time-of-flight
ASJC Scopus subject areas
- General Chemistry
- Biochemistry
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