Preparation of thin tissue sections for imaging mass spectrometry
View Patent ↗The invention relates to the preparation of thin tissue sections for mass spectrometric (MALDI) imaging, and proposes a method wherein a microcrystalline layer of the matrix material is produced on the surface of the thin tissue sections, and soluble analyte molecules are transported orthogonally through the thin tissue section to the matrix layer, without substantial lateral diffusion, by means of a solvent flow with alternating or constant direction, and are then deposited in the matrix layer and, if possible, embedded in the matrix crystals. A solvent flow which alternates in direction can be produced by successive, alternating phases of swelling and drying, brought about by periodic changes to the thin tissue section temperature and/or the partial pressures of the solvents. A continuous solvent flow can be generated by applying the thin tissue section onto a porous support which supplies solvent to the rear surface of the thin tissue section.
1. A method for the preparation of a thin tissue section whose surface is provided with a matrix layer for the acquisition of a mass-spectrometric image using ionization by matrix-assisted laser desorption, the method comprising transporting analyte molecules from various layers of the thin tissue section straight through the thin tissue section to the matrix layer at the surface of the thin tissue section by means of generating a solvent flow with alternating direction, which solvent flow is generated by alternate swelling and drying of the thin tissue section brought about by one of changing the partial pressure of a solvent in the ambient gas, changing a temperature of the thin tissue section, and changing both the temperature and the partial pressure, wherein the method is carried out in a chamber in which an ambient gas pressure is kept that is below atmospheric pressure.
2. The method according to claim 1 , wherein the ambient gas pressure in the chamber is kept at less than 10 4 pascal.
3. The method according to claim 1 , wherein the temperature of the thin tissue section or the partial pressure of the solvent in the ambient gas are changed such as to avoid the formation of dew on the thin tissue section.
4. The method according to claim 1 , wherein the partial pressure is changed by compressing the gas volume.
5. The method according to claim 1 , wherein the partial pressure is changed by alternately feeding-in solvent vapor and neutral gas.
6. The method according to claim 1 , wherein several solvents are used to transport the analyte molecules, and the partial pressures of the individual solvents are controlled in such a way that each solvent participates in the swelling of the thin tissue section.
7. The method according to claim 1 , wherein the matrix layer is applied to the tissue section in the chamber, and wherein the solvent flow is generated alternatingly with the application of the matrix layer.
8. The method according to claim 1 , wherein the matrix layer is applied to the tissue section in the chamber, and wherein the solvent flow is generated while the matrix layer is growing.
9. The method according to claim 1 , wherein the matrix layer is applied by resublimation in the chamber.
10. The method according to claim 9 , wherein the resublimation is assisted by crystal nuclei, which are applied to the thin tissue section before the resublimation.
11. The method according to claim 10 , wherein the crystal nuclei consist of a fine crystalline powder whose lattice constant and crystal shapes are similar to the crystals of the matrix substance.
12. The method according to claim 10 , wherein the crystal nuclei consist of fine matrix crystal powder.
13. The method according to claim 1 , wherein during the phases where the solvent flow in the thin tissue section transports the analyte molecules to the matrix layer, a liquid film is produced in the matrix layer, in which the analyte molecules can reach the surface of the matrix crystals.
14. The method according to claim 1 , wherein the matrix layer is applied, after locating the tissue section in the chamber, as snow generated by spraying a matrix solution with immediate drying of droplets after they have exited from a spray capillary before the resultant snow is deposited on the surface of the thin tissue section.
15. The method according to claim 14 , wherein the snow is stuck together by condensation of a solvent.
16. The method according to claim 1 , wherein the matrix layer comprises a material applied dry to the thin tissue section in order to avoid lateral flows of solvents and any lateral transport of analyte molecules within the thin tissue section and on its surface.
17. The method according to claim 16 , wherein the application of the dry matrix layer and the alternate swelling and drying of the thin tissue section are conducted in the chamber.