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Infrared mass spectrometric imaging below the diffraction limit

  • Stefan L. Luxembourg
  • , Liam A. McDonnell
  • , Todd H. Mize
  • , Ron M.A. Heeren*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)671-673
Number of pages3
JournalJournal of Proteome Research
Volume4
Issue number3
DOIs
Publication statusPublished - May 2005
Externally publishedYes

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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