Reduced dimensionality structured illumination microscopy with patterned arrays of nanowells

Patent metadata

Field	Value
Publication number	US-11933728-B2
Application number	US-202318154405-A
Country	US
Kind code	B2
Filing date	Jan 13, 2023
Priority date	Jan 24, 2018
Publication date	Mar 19, 2024
Grant date	Mar 19, 2024

Abstract

Techniques are described for reducing the number of angles needed in structured illumination imaging of biological samples through the use of patterned flowcells, where nanowells of the patterned flowcells are arranged in, e.g., a square array, or an asymmetrical array. Accordingly, the number of images needed to resolve details of the biological samples is reduced. Techniques are also described for combining structured illumination imaging with line scanning using the patterned flowcells.

First claim

What is claimed is:

1. An apparatus, comprising:
an asymmetrically patterned flowcell comprising a plurality of elongated nanowells to contain a biological sample;
a light emitter to project an optical pattern onto the biological sample contained in the flowcell;
a camera assembly to capture a plurality of images of the optical pattern overlaid on the biological sample, the plurality of images reflecting a first phase, a second phase, and a third phase of the optical pattern relative to the biological sample; and
a processor to reconstruct a high resolution image representative of the biological sample based on a combination of the plurality of images; wherein the asymmetrically patterned flowcell and the plurality of elongated nanowells reduce a number of the plurality of images required to reconstruct the high resolution image representative of the biological sample.

2. The apparatus of claim 1 , wherein each of the elongated nanowells is elliptically shaped or rectangularly shaped.

3. The apparatus of claim 2 , wherein the flowcell comprises a substrate comprising the elongated nanowells.

4. The apparatus of claim 3 , further comprising a translucent cover coupled to the substrate and covering the elongated nanowells.

5. The apparatus of claim 3 , wherein the elongated nanowells form a lane.

6. The apparatus of claim 3 , wherein the elongated nanowells form a plurality of spaced-apart lanes.

7. The apparatus of claim 3 , wherein each of the plurality of elongated nanowells are oriented such that along a first axis of the asymmetrically patterned flowcell, resolution is increased to resolve information representative of the biological sample.

8. The apparatus of claim 3 , wherein each of the plurality of elongated nanowells are oriented such that along a second axis of the asymmetrically patterned flowcell, resolution is not increased to resolve information representative of the biological sample.

9. The apparatus of claim 1 , comprising a light structuring optical assembly positioned in front of the light source to project the optical pattern onto the biological sample.

10. The apparatus of claim 9 , wherein the light structuring optical assembly comprises one or more optical diffraction gratings.

11. The apparatus of claim 10 , wherein the one or more optical diffraction gratings comprise one-dimensional or two-dimensional transmissive, reflective, or phase gratings.

12. The apparatus of claim 10 , wherein the one or more optical diffraction gratings are fixed.

13. The apparatus of claim 10 , wherein the one or more optical diffraction gratings comprise two fixed one-dimensional transmissive diffraction gratings oriented substantially perpendicular to each other.

14. An apparatus, comprising:
an asymmetrically patterned flowcell comprising a plurality of elongated nanowells to contain a biological sample;
a first light source to emit a first light in a first wavelength;
a second light source to emit a second light in a second wavelength, different from the first wavelength;
a beam shaping lens to shape the first light and the second light into a line pattern and project the line pattern onto the biological sample;
a camera assembly to capture a plurality of images of the optical pattern overlaid on the biological sample, the plurality of images reflecting a first phase, a second phase, and a third phase of the optical pattern relative to the biological sample; and
a processor to reconstruct a high resolution image representative of the biological sample based on a combination of the plurality of images.

15. The apparatus of claim 14 , wherein the first light source and the second light source are lasers.

16. The apparatus of claim 14 , wherein the camera assembly is a time delay integration line scanning camera assembly.

17. The apparatus of claim 14 , further comprising a diffraction grating and wherein first light source and the second light source are movable relative to the diffraction grating.

18. The apparatus of claim 14 , further comprising a stage on which the asymmetrically patterned flowcell is to be positioned, the stage to move the asymmetrically patterned flowcell relative to the line pattern.

19. A method, comprising:
emitting a first light in a first wavelength from a first light source;
emitting a second light in a second wavelength, different from the first wavelength, from a second light source;
shaping the first light and the second light into a line pattern and projecting the line pattern onto a biological sample contained in a flowcell comprising a plurality of elongated nanowells;
capturing a plurality of line scans of the line pattern;
reconstructing, using a processor, a high resolution image representative of the biological sample based on a combination of the plurality of line scans.

20. The method of claim 19 , wherein at least one of the first and second light sources and/or the biological sample is moved between each of the plurality of line scans.

21. The method of claim 19 , wherein the first light and the second light are shaped into the line pattern through a beam shaping lens.

22. The method of claim 19 , wherein the plurality of line scans are captured using a time delay integration line scanning camera assembly.

23. The method of claim 19 , wherein the first light and the second light are shaped into the line pattern through a stationary optical diffraction grating.

24. The method of claim 23 , wherein the biological sample is moved between each of the plurality of line scans.

25. The method of claim 23 , comprising operating the first light source and the second light source in a pulsed fashion such that the first light and the second light are not emitted as the biological sample is being moved.

Assignees

• Illumina Inc
• Illumina Cambridge Ltd

Inventors

• Skinner Gary
• Evans Geraint
• Hong Stanley

Classifications

• G01N21/6452 Primary

  Individual samples arranged in a regular 2D-array, e.g. multiwell plates · CPC title

• B01L3/5085

  for multiple samples, e.g. microtitration plates · CPC title

• G01N21/05

  Flow-through cuvettes (G01N21/09 takes precedence; handling fluid samples G01N1/10) · CPC title

• G02B21/06

  Means for illuminating specimens · CPC title

• G02B21/16

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