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Sublimation As a Method of Matrix Application for Mass Spectrometric Imaging

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Specialty Chemistry
Date 2007 Jul 31
PMID 17659880
Citations 224
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Abstract

Common organic matrix-assisted laser desorption/ionization (MALDI) matrices, 2,5-dihydroxybenzoic acid, 3,5-dimethoxy-4-hydroxycinnamic acid, and alpha-cyano-4-hydroxycinnamic acid, were found to undergo sublimation without decomposition under conditions of reduced pressure and elevated temperature. This solid to vapor-phase transition was exploited to apply MALDI matrix onto tissue samples over a broad surface in a solvent-free application for mass spectrometric imaging. Sublimation of matrix produced an even layer of small crystals across the sample plate. The deposition was readily controlled with time, temperature, and pressure settings and was highly reproducible from one sample to the next. Mass spectrometric images acquired from phospholipid standards robotically spotted onto a MALDI plate yielded a more intense, even signal with fewer sodium adducts when matrix was applied by sublimation relative to samples where matrix was deposited by an electrospray technique. MALDI matrix could be readily applied to tissue sections on glass slides and stainless steel MALDI plate inserts as long as good thermal contact was made with the condenser of the sublimation device. Sections of mouse brain were coated with matrix applied by sublimation and were imaged using a Q-q-TOF mass spectrometer to yield mass spectral images of very high quality. Image quality is likely enhanced by several features of this technique including the microcrystalline morphology of the deposited matrix, increased purity of deposited matrix, and evenness of deposition. This inexpensive method was reproducible and eliminated the potential for spreading of analytes arising from solvent deposition during matrix application.

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References
1.
Jurchen J, Rubakhin S, Sweedler J . MALDI-MS imaging of features smaller than the size of the laser beam. J Am Soc Mass Spectrom. 2005; 16(10):1654-9. DOI: 10.1016/j.jasms.2005.06.006. View

2.
Touboul D, Kollmer F, Niehuis E, Brunelle A, Laprevote O . Improvement of biological time-of-flight-secondary ion mass spectrometry imaging with a bismuth cluster ion source. J Am Soc Mass Spectrom. 2005; 16(10):1608-18. DOI: 10.1016/j.jasms.2005.06.005. View

3.
Lechene C, Hillion F, McMahon G, Benson D, Kleinfeld A, Kampf J . High-resolution quantitative imaging of mammalian and bacterial cells using stable isotope mass spectrometry. J Biol. 2006; 5(6):20. PMC: 1781526. DOI: 10.1186/jbiol42. View

4.
Jackson S, Wang H, Woods A . In situ structural characterization of glycerophospholipids and sulfatides in brain tissue using MALDI-MS/MS. J Am Soc Mass Spectrom. 2006; 18(1):17-26. DOI: 10.1016/j.jasms.2006.08.015. View

5.
Jackson S, Wang H, Woods A . In situ structural characterization of phosphatidylcholines in brain tissue using MALDI-MS/MS. J Am Soc Mass Spectrom. 2005; 16(12):2052-6. DOI: 10.1016/j.jasms.2005.08.014. View