Multiplexed tissue imaging
An apparatus attaches to a microscope slide to form an enclosed fluidic chamber with input and output ports, where a tissue or cell sample on the slide can be processed using techniques such as immunohistochemical staining. Flow of reagents within the chamber can be laminar and highly uniform across the sample surface to achieve staining that is free of gradients. The sample can be imaged prior to, during, or after any given processing step. Methods for staining and imaging a sample can be implemented through one or more rounds of labeling, label removal or erasure and imaging. Samples can be imaged many times to achieve very high multiplexing levels. Samples can be placed on an imaging apparatus at various times and removed from the imaging apparatus for certain steps.
1. A method for analyzing a biological sample, the method comprising:
obtaining a biological sample mounted on a first substrate;
affixing a second substrate to the first substrate to form an enclosed chamber on the first substrate with the biological sample positioned within an interior volume of the enclosed chamber, wherein the second substrate comprises a first port formed by a first aperture extending through a thickness of the second substrate and a second port formed by a second aperture extending through the thickness of the second substrate;
introducing a composition into the interior volume through the first port, wherein the composition comprises multiple different types of capture agents, each of the different types of capture agents comprising a different type of binding agent that selectively binds to a different sample component and an oligonucleotide linked to the binding agent that is specific to each different type of binding agent, wherein each of the different types of capture agents is bound to the biological sample by introducing the different types of capture agents at the same time into the interior volume of the enclosed chamber; and
performing multiple imaging cycles, wherein each imaging cycle comprises:
(a) binding a probe to the biological sample;
(b) obtaining an image of the bound probe in the biological sample; and
(c) removing at least a portion of the probe from the biological sample,
wherein a thickness of the interior volume between the first and second substrates is 250 micrometers or less.
2. The method of claim 1 , wherein the first substrate is formed of a substantially transparent material.
3. The method of claim 1 , wherein the second substrate comprises a window.
4. The method of claim 1 , further comprising positioning a gasket between the first and second substrates, wherein the gasket is formed of an adhesive material.
5. The method of claim 1 , further comprising, prior to affixing the second substrate to the first substrate:
incubating the biological sample in acetone;
removing residual acetone from the biological sample; and
affixing the second substrate to the first substrate following the removal of residual acetone.
6. The method of claim 1 , further comprising, prior to performing the multiple imaging cycles, applying a stain to the biological sample.
7. The method of claim 1 , wherein the interior volume is 0.20 cm 3 or less.
8. The method of claim 1 , wherein during each imaging cycle, the probe is bound to the biological sample by introducing a composition comprising the probe through the first port, and removing components of the composition through the second port.
9. The method of claim 1 , wherein binding the probe to the biological sample comprises binding one or more different types of probes to the biological sample, wherein each different type of probe comprises a different type of oligonucleotide linked to a labeling agent that is specific to each different type of oligonucleotide.
10. The method of claim 9 , wherein the one or more different types of probes are bound to the biological sample at the same time by introducing a composition comprising the one or more different types of probes into the interior volume of the enclosed chamber, and wherein the one or more different types of probes bind to corresponding different types of capture agents in the biological sample.
11. A method for analyzing a biological sample, the method comprising:
obtaining a biological sample mounted on a first substrate;
affixing a second substrate to the first substrate to form an enclosed chamber on the first substrate with the biological sample positioned within an interior volume of the enclosed chamber, wherein the second substrate comprises a first port formed by a first aperture extending through a thickness of the second substrate and a second port formed by a second aperture extending through the thickness of the second substrate;
introducing a composition comprising multiple different types of capture agents through the first port, each of the different types of capture agents comprising a different type of binding agent that selectively binds to a different sample component and an oligonucleotide linked to the binding agent that is specific to each different type of binding agent; and
performing multiple imaging cycles, wherein each imaging cycle comprises:
(a) binding a probe to the biological sample;
(b) obtaining an image of the bound probe in the biological sample; and
(c) removing at least a portion of the probe from the biological sample,
wherein the first and second substrates are substantially transparent; and
wherein an imaging window formed by the first and second substrates has a field of view of at least 500 mm 2 .
12. The method of claim 11 , wherein the first substrate comprises a microscope slide.
13. The method of claim 11 , wherein the second substrate comprises a window.
14. The method of claim 11 , further comprising positioning a gasket between the first and second substrates, wherein the gasket is formed of an adhesive material.
15. The method of claim 11 , further comprising, prior to affixing the second substrate to the first substrate:
incubating the biological sample in acetone;
removing residual acetone from the biological sample; and
affixing the second substrate to the first substrate following the removal of residual acetone.
16. The method of claim 11 , further comprising, prior to performing the multiple imaging cycles, applying a stain to the biological sample.
17. The method of claim 11 , wherein a minimum distance between the first and second ports measured in a plane of the second substrate is 20 mm or more.
18. The method of claim 11 , wherein during each imaging cycle, the probe is bound to the biological sample by introducing a composition comprising the probe through the first port, and removing components of the composition through the second port.
19. The method of claim 11 , wherein each of the different types of capture agents is bound to the biological sample by introducing the composition comprising each of the different types of capture agents at the same time into the interior volume of the enclosed chamber.
20. The method of claim 16 , wherein binding the probe to the biological sample comprises binding one or more different types of probes to the biological sample, wherein each different type of probe comprises a different type of oligonucleotide linked to a labeling agent that is specific to each different type of oligonucleotide.
21. The method of claim 16 , further comprising, prior to introducing the composition into the interior volume of the enclosed chamber, connecting a port coupler to at least one of the first and second ports.
22. A method for analyzing a biological sample, the method comprising:
obtaining a biological sample mounted on a first substrate;
affixing a second substrate to the first substrate to form an enclosed chamber on the first substrate with the biological sample positioned within an interior volume of the enclosed chamber, wherein the second substrate comprises a first port formed by a first aperture extending through a thickness of the second substrate and a second port formed by a second aperture extending through the thickness of the second substrate, and wherein compositions are introduced into the interior volume through the first port;
prior to introducing a composition into the interior volume of the enclosed chamber, connecting a port coupler to at least one of the first and second ports; and
performing multiple imaging cycles, wherein each imaging cycle comprises:
(a) binding a probe to the biological sample;
(b) obtaining an image of the bound probe in the biological sample; and
(c) removing at least a portion of the probe from the biological sample,
wherein the first and second substrates are substantially transparent.
23. The method of claim 22 , wherein the first substrate is formed of a substantially transparent material.
24. The method of claim 22 , wherein the second substrate comprises a window.
25. The method of claim 22 , further comprising positioning a gasket between the first and second substrates, wherein the gasket is formed of an adhesive material.
26. The method of claim 22 , further comprising, prior to affixing the second substrate to the first substrate:
incubating the biological sample in acetone;
removing residual acetone from the biological sample; and
affixing the second substrate to the first substrate following the removal of residual acetone.
27. The method of claim 22 , further comprising, prior to performing the multiple imaging cycles, applying a stain to the biological sample.
28. The method of claim 22 , wherein during each imaging cycle, the probe is bound to the biological sample by introducing a composition comprising the probe through the first port, and removing components of the composition through the second port.
29. The method of claim 22 , further comprising, prior to performing the multiple imaging cycles, binding a capture agent to the biological sample by introducing a composition comprising the capture agent through the first port.
30. The method of claim 29 , wherein the capture agent comprises a binding agent that selectively binds to a sample component, and an oligonucleotide that is linked to the binding agent.
31. The method of claim 30 , wherein the composition comprises multiple different types of capture agents, each of the different types of capture agents comprising a different type of binding agent that selectively binds to a different sample component, and an oligonucleotide that is specific to each different type of binding agent.
32. The method of claim 31 , wherein each of the different types of capture agents is bound to the biological sample by introducing the composition comprising each of the different types of capture agents at the same time into the interior volume of the enclosed chamber.
33. The method of claim 22 , wherein binding the probe to the biological sample comprises binding one or more different types of probes to the biological sample, wherein each different type of probe comprises a different type of oligonucleotide linked to a labeling agent that is specific to each different type of oligonucleotide.
34. The method of claim 33 , wherein the one or more different types of probes are bound to the biological sample at the same time by introducing a composition comprising the one or more different types of probes into the interior volume of the enclosed chamber, and wherein the one or more different types of probes bind to corresponding different types of capture agents in the biological sample.
35. The method of claim 22 , wherein the interior volume is 0.20 cm 3 or less.