Laser ablation cell

Patent metadata

Field	Value
Publication number	US-9496124-B2
Application number	US-201414223606-A
Country	US
Kind code	B2
Filing date	Mar 24, 2014
Priority date	Mar 22, 2013
Publication date	Nov 15, 2016
Grant date	Nov 15, 2016

Abstract

A laser ablation cell ( 1 ) comprises a flow channel ( 11 ) having an essentially constant cross-sectional area so as to ensure a strictly laminar flow in the flow channel. A sample chamber ( 21 ) is provided adjacent to a lateral opening ( 14 ) of the flow channel. A laser beam ( 41 ) enters the sample chamber ( 21 ) through a lateral window ( 16 ) and impinges on a surface ( 24 ) of a sample ( 23 ) to ablate material from the sample. The sample may be positioned in such a distance from the flow channel that the laser-generated aerosol mass distribution has its center within the flow channel. This leads to short aerosol washout times. The laser ablation cell is particularly well suited for aerosol generation in inductively coupled plasma mass spectrometry (ICPMS), including imaging applications.

First claim

What is claimed is:

1. A method of imaging a biological sample comprising a plurality of cells, the method comprising steps of:
(i) labelling at least one of a plurality of different target molecules in the biological sample with at least one of a plurality of different lanthanide labelling atoms, wherein each different labelling atom is attached to a different specific labelling construct, to provide a labelled biological sample;
(ii) subjecting multiple cells of the labelled biological sample to laser ablation with a resolution at a cellular level or better at multiple known locations, to form a plurality of plumes; and
(iii) subjecting plumes to inductively coupled plasma mass spectrometry;
(iv) detecting the at least one labelling atoms in the plumes at the multiple known locations; and
(v) constructing a cellular or subcellular level resolution image of the biological sample based the detection of the at least one labelling atoms in the plumes.

2. The method of claim 1 , wherein subjecting multiple cells of the labelled biological sample to laser ablation comprises subjecting the multiple cells to laser ablation with a laser spot size of less than 25 μm at multiple known locations.

3. The method of claim 1 , wherein labelling at least one of the plurality of different target molecules comprises labelling at least three different target molecules in the biological sample with at least three different labelling atoms.

4. The method of claim 1 , wherein a plurality of different target molecules in the biological sample are labelled with a plurality of different labelling atoms and wherein the labels can be distinguished by LA-ICP-MS to identify each of the at least one different target molecules.

5. The method of claim 1 , wherein the cellular or subcellular level resolution image constructed based the detection of the at least one labelling atoms in the plumes has a resolution of less than 2 μm.

6. The method of claim 1 , wherein the cellular or subcellular level resolution image has a subcellular resolution and laser ablation of the sample occurs at a frequency of at least 10 Hz.

7. A method of imaging a biological sample comprising a plurality of cells, the method comprising steps of:
(i) labelling at least one of a plurality of different target molecules in the biological sample with at least one of a plurality of different lanthanide labelling atoms, wherein each different labelling atom is attached to a different specific labelling construct, to provide a labelled biological sample;
(ii) subjecting multiple cells of the labelled biological sample to laser ablation with a resolution at a cellular level or better at multiple known locations, to form a plurality of plumes; and
(iii) subjecting plumes to inductively coupled plasma mass spectrometry, whereby detection of the at least one labelling atoms in the plumes permits construction of an image of the biological sample;
wherein laser ablation occurs in an ablation cell having a washout time of 100 ms or less.

8. The method of claim 1 , wherein laser ablation occurs (i) in an ablation cell having a washout time of 30 ms or less and (ii) at a frequency of at least 20 Hz.

9. The method of claim 1 , wherein at least 20 different labelling atoms having different atomic masses are used.

10. The method of claim 1 , wherein the mass spectrometry steps uses time-of-flight detection.

11. The method of claim 1 , wherein each different labelling atom is attached to a different specific labelling construct.

12. The method of claim 1 , wherein at least one intracellular target and at least one cell surface target are labelled.

13. The method of claim 1 , wherein the biological sample is a tissue sample, a monolayer of adherent cells, cells immobilised on a solid surface, or a biofilm.

14. A method of imaging a biological sample comprising a plurality of cells, the method comprising:
ablating portions of a biological sample in a laser ablation cell with a laser to form a series of plumes, the biological sample comprising one or more target molecules labelled with metal atoms;
washing out the series of plumes with a gas from the laser ablation cell and toward an inductively coupled plasma;
subjecting plumes to inductively coupled plasma mass spectrometry;
detecting the metal atoms in the plumes; and
constructing a cellular or subcellular level resolution image of the biological sample based the detection of the metal atoms in the plumes.

15. The method of claim 14 , wherein the plumes are washed out from the laser ablation cell with the gas in under 100 ms after formation by the laser.

16. The method of claim 14 , wherein the series of plumes are washed out from the laser ablation cell toward the inductively coupled plasma such that overlap between signals originating from consecutive plumes is less than 10 percent in intensity.

17. The method of claim 14 , wherein the laser has a spot size of 0.2-2 μm.

18. The method of claim 14 , wherein ablating portions of the biological sample comprises raster scanning the laser over the sample.

19. The method of claim 14 , wherein the laser ablation cell comprises a cell top coupled with a cell bottom, the cell top having a flow channel and the cell bottom having a sample chamber, wherein the flow channel includes an inlet for a carrier gas to be directed through the flow channel; wherein the cell bottom includes an inlet for a sheath gas to be directed through the sample chamber; and wherein the sheath gas and carrier gas are configured to combine an exit as a mixed-gas stream at an outlet of the flow channel of the cell top.

20. The method of claim 19 , wherein the carrier gas comprises Argon, and wherein the sheath gas comprises Helium.

Assignees

• ETH Zürich
• Scherrer Inst Paul
• Eth Zuerich

Inventors

• Günther Detlef
• Grolimund Daniel
• Wang Hao

Classifications

• G01N33/57515

  of the breast · CPC title

• H01J49/0463

  Desorption by laser or particle beam, followed by ionisation as a separate step (sample holder per se H01J49/0418) · CPC title

• H01J49/40

  Time-of-flight spectrometers (H01J49/36 takes precedence) · CPC title

• H01J49/04 Primary

  Arrangements for introducing or extracting samples to be analysed, e.g. vacuum locks; Arrangements for external adjustment of electron- or ion-optical components · CPC title

• G01N33/6848

  Methods of protein analysis involving mass spectrometry · CPC title