Selective plane illumination microscopy (SPIM) systems and methods

Patent metadata

Field	Value
Publication number	US-10139608-B2
Application number	US-201515516620-A
Country	US
Kind code	B2
Filing date	Oct 2, 2015
Priority date	Oct 2, 2014
Publication date	Nov 27, 2018
Grant date	Nov 27, 2018

Abstract

In one embodiment, a selective plane illumination microscopy system for capturing light emitted by an illuminated specimen includes a specimen stage having a top surface adapted to support a specimen holder and an opening adapted to provide access to a bottom of the holder, and a selective plane illumination microscopy optical system positioned beneath the stage, the optical system including an excitation objective, a detection objective, and an open-top, hollow prism that is adapted to contain a liquid, wherein the prism is positioned within the opening of the stage and optical axes of the objectives are aligned with the prism such that the axes pass through the prism and intersect at a position near the top surface of the specimen stage.

First claim

The invention claimed is:

1. A selective plane illumination microscopy system for capturing light emitted by an illuminated specimen, the system comprising:
a specimen stage having a top surface adapted to support a specimen holder and an opening adapted to provide access to a bottom of the holder; and
a selective plane illumination microscopy optical system positioned beneath the stage, the optical system configured to illuminate the specimen with a sheet of excitation light and including an excitation objective, a detection objective, and an open-top, hollow prism that is adapted to contain a liquid, wherein the prism is positioned within the opening of the stage and optical axes of the objectives are aligned with the prism such that the axes pass through the prism and intersect at a position near the top surface of the specimen stage.

2. The system of claim 1 , wherein the stage is motorized so as to be capable of being scanned in x and y directions.

3. The system of claim 1 , wherein the optical axes of the excitation and detection objectives form an angle of approximately 45 degrees with the open top of the prism and form an angle of approximately 90 degrees with each other.

4. The system of claim 1 , wherein prism is positioned within the opening of the stage such that a top surface of the prism is generally level with the top surface of the stage so that the liquid contacts the bottom of the specimen holder when the prism is filled with the liquid.

5. The system of claim 1 , wherein the prism comprises windows through which light from the optical system enters and exits the prism when the system is operated.

6. The system of claim 5 , wherein the excitation and detection objectives are air objectives positioned outside of the prism.

7. The system of claim 1 , wherein the prism comprises openings through which light from the optical system enters and exits the prism when the system is operated.

8. The system of claim 7 , wherein the excitation and detection objectives are dipping objectives positioned in the openings such that they are immersed in the liquid when the prism is filled with the liquid.

9. The system of claim 8 , wherein the optical system further comprises an adaptive optics element configured to compensate for aberration created by the detection objective.

10. The system of claim 9 , wherein the adaptive optics element comprises a deformable mirror.

11. The system of claim 9 , wherein the adaptive optics element comprises a spatial light modulator.

12. The system of claim 1 , wherein the optical system further comprises a cylindrical lens that forms a sheet of excitation light that is focused by the excitation objective to be coincident with the specimen and a focal plane of the detection objective.

13. The system of claim 1 , wherein the optical system further comprises a laser that generates the light.

14. The system of claim 1 , further comprising a light sensor that receives fluorescence emitted from the specimen.

15. An imaging prism for use in an opening provided within a microscope stage, the prism comprising:
a body having a generally triangular cross-section that defines a hollow space;
angled lower sides through which light can enter and exit the prism, the sides comprising openings through which the light passes; and
an open top adapted to be positioned level with a top surface of the microscope stage;
wherein the prism is configured to be filled with a liquid such that a top surface of the liquid is positioned so as to contact a bottom surface of a specimen holder supported on top of the microscope stage.

16. The imaging prism of claim 15 , wherein windows are positioned within the openings to seal the openings.

17. A method for performing selective plane illumination microscopy on a specimen, the method comprising:
positioning an open-top, hollow prism adapted to contain a liquid in an opening formed in a microscope stage, wherein the prism is positioned such that its open top is generally level with a top surface of the stage;
positioning an excitation objective and an detection objective of a selective plane illumination microscopy optical system below the stage such that the optical axes of the objectives pass through the prism and intersect at a position near the top surface of the specimen stage;
illuminating the specimen contained in a specimen holder supported on the top surface of the stage with a sheet of laser light focused by the excitation objective; and
capturing light emitted by the specimen that passes through the detection objective.

18. The method of claim 17 , wherein positioning an excitation objective and a detection objective comprises positioning the objectives outside of the prism such that they are not immersed in the liquid.

19. The method of claim 17 , wherein positioning an excitation objective and a detection objective comprises positioning the objectives inside of the prism such that they are immersed in the liquid.

Assignees

• Univ California

Inventors

• Huang Bo
• Mcgorty Ryan

Classifications

• G02B21/367

  providing an output produced by processing a plurality of individual source images, e.g. image tiling, montage, composite images, depth sectioning, image comparison · CPC title

• G02B21/24

  Base structure · CPC title

• G02B21/16

  adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title

• G02B21/0088 Primary

  Inverse microscopes · CPC title

• G02B5/06

  Fluid-filled or evacuated prisms · CPC title