Abstract
Matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) combined with laser-induced postionization for MALDI-2 enables the simultaneous registration of numerous classes of small molecules (e.g., secondary metabolites including sterols) as well as phospholipids, glycolipids, and glycans from tissue sections and from cell cultures with strongly boosted ion yields. Here, we describe methodological aspects that are key for optimizing the analytical sensitivity and spatial resolution of a MALDI-2 imaging experiment. We will include both top-illumination MALDI-2 as well as the recently introduced transmission (t-) mode MALDI-2 approach.
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Acknowledgments
We acknowledge the invaluable input and support from numerous expert colleagues, many of whom are listed as coauthors on the cited papers. Financial support by the German Research Foundation (DFG; grants DR416/9-1, project number 208319078, to K.D.; DR416/12-1 and SO976/3-1, project number 290343045, to K.D. and J.S.; and SO976/5-1, project number 400912714, to J.S.) and the Interdisciplinary Center for Clinical Research (IZKF) of the Münster University Medical School (grant Drei2/018/17, to K.D. and J.S.) is gratefully acknowledged.
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Dreisewerd, K., Bien, T., Soltwisch, J. (2022). MALDI-2 and t-MALDI-2 Mass Spectrometry Imaging. In: Lee, YJ. (eds) Mass Spectrometry Imaging of Small Molecules. Methods in Molecular Biology, vol 2437. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2030-4_2
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DOI: https://doi.org/10.1007/978-1-0716-2030-4_2
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