Abstract
Mass spectrometry imaging (MSI) is a powerful tool in metabolomics and proteomics for the spatial localization and identification of pharmaceuticals, metabolites, lipids, peptides and proteins in biological tissues. However, sample preparation remains a crucial variable in obtaining the most accurate distributions. Common washing steps used to remove salts, and solvent-based matrix application, allow analyte spreading to occur. Solvent-free matrix applications can reduce this risk, but increase the possibility of ionisation bias due to matrix adhesion to tissue sections. We report here the use of matrix-free MSI using laser desorption ionisation performed on a 12 T Fourier transform ion cyclotron resonance (FTICR) mass spectrometer. We used unprocessed tissue with no post-processing following thaw-mounting on matrix-assisted laser desorption ionisation (MALDI) indium-tin oxide (ITO) target plates. The identification and distribution of a range of phospholipids in mouse brain and kidney sections are presented and compared with previously published MALDI time-of-flight (TOF) MSI distributions.
Original language | English |
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Pages (from-to) | 969-72 |
Number of pages | 4 |
Journal | Rapid communications in mass spectrometry |
Volume | 25 |
Issue number | 7 |
Early online date | 14 Mar 2011 |
DOIs | |
Publication status | Published - 15 Apr 2011 |
Keywords
- animals
- brain chemistry
- Fourier analysis
- histocytochemistry
- kidney
- metabolomics
- mice
- phospholipids
- spectrometry
- tin compounds
- mass
- matrix-assisted laser desorption-ionization