IP Library Granted Patent US 11,384,386
Granted Patent B2
US 11,384,386 · App. 17/030,230 · Granted Jul 12, 2022

Spatially encoded biological assays

Inventor: Mark S. Chee (San Diego, CA)
Assignee: Prognosys Biosciences, Inc.
C12Q1/6837B01L3/502715C12Q1/68C12Q1/6804C12Q1/6809C12Q1/6834C12Q1/6841C12Q1/6869C12Q1/6874C12Q1/6876C40B30/04C40B60/04G01N33/5308G01N33/543G01N33/54366G01N33/6845G01N2458/10
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Quick Facts
Patent No.
US 11,384,386
App. No.
17/030,230
Filed
Sep 23, 2020
Granted
Jul 12, 2022
Kind
B2
Art Unit
1634
USPC
506/16
Abstract

The present invention provides assays and assay systems for use in spatially encoded biological assays. The invention provides an assay system comprising an assay capable of high levels of multiplexing where reagents are provided to a biological sample in defined spatial patterns; instrumentation capable of controlled delivery of reagents according to the spatial patterns; and a decoding scheme providing a readout that is digital in nature.

Claims (35)

1. A composition comprising an array comprising a planar substrate and a plurality of capture probes, wherein:

each of the plurality of capture probes comprises: (i) a biological target-binding domain, (ii) a coding tag comprising a nucleic acid sequence, and (iii) a primer binding site;

the biological target-binding domain of each capture probe of the plurality of capture probes comprises a nucleic acid sequence complementary to a portion of an mRNA;

the nucleic acid sequence of the coding tag of each of the plurality of capture probes identifies a unique location on the planar substrate and does not selectively hybridize to the mRNA that binds to the biological target-binding domain of the capture probe; and

the plurality of capture probes are directly immobilized on the planar substrate in a pre-defined pattern.

2. The composition of claim 1 , wherein the pre-defined pattern is a pattern of ink jet-printed or photolithographic features.

3. The composition of claim 1 , wherein 5′ ends of each of the plurality of capture probes are attached to the planar substrate.

4. The composition of claim 1 , wherein the planar substrate comprises a slide.

5. The composition of claim 1 , wherein the plurality of capture probes comprises at least 1,000 capture probes.

6. The composition of claim 5 , wherein the plurality of capture probes comprises at least 10,000 capture probes.

7. The composition of claim 1 , wherein the array further comprises a fiducial marker.

8. The composition of claim 1 , wherein the composition further comprises a biological sample disposed on the array.

9. The composition of claim 8 , wherein the biological sample is a tissue sample.

10. The composition of claim 9 , wherein the tissue sample comprises a tissue section.

11. The composition of claim 10 , wherein the tissue section is a fixed tissue section.

12. The composition of claim 11 , wherein the fixed tissue section is a formalin-fixed paraffin-embedded tissue sample.

13. The composition of claim 9 , wherein the tissue sample is a fresh, frozen tissue sample.

14. The composition of claim 1 , wherein the composition further comprises the mRNA selectively hybridized to a biological target-binding domain of at least one of the plurality of capture probes.

15. The composition of claim 1 , wherein the biological target-binding domain is the same for each of the plurality of capture probes.

16. A composition comprising (i) an array comprising a planar substrate and a plurality of capture probes, and (ii) a tissue sample, wherein:

the tissue sample is disposed on the array;

each of the plurality of capture probes comprises: (i) a biological target-binding domain (ii) a coding tag comprising a nucleic acid sequence, and (iii) a primer binding site;

the biological target-binding domain of each probe of the plurality of capture probes comprises a nucleic acid sequence complementary to a portion of an mRNA;

the nucleic acid sequence of the coding tag of each of the plurality of capture probes identifies a unique location on the planar substrate; and

the plurality of capture probes are directly immobilized on the planar substrate in a pre-defined pattern.

17. The composition of claim 16 , wherein the planar substrate comprises a slide.

18. The composition of claim 16 , wherein the plurality of capture probes comprises at least 1,000 capture probes.

19. The composition of claim 16 , wherein the array further comprises a fiducial marker.

20. The composition of claim 16 , wherein the tissue sample comprises a tissue section.

21. The composition of claim 20 , wherein the tissue section is a fixed tissue section.

22. The composition of claim 21 , wherein the fixed tissue section is a formalin-fixed paraffin-embedded tissue sample.

23. The composition of claim 16 , wherein the tissue sample is a fresh, frozen tissue sample.

24. The composition of claim 16 , wherein the composition further comprises the mRNA selectively hybridized to a biological target-binding domain of at least one of the plurality of capture probes.

25. The composition of claim 16 , wherein the nucleic acid sequence of the coding tag of each of the plurality of capture probes does not selectively hybridize to the mRNA.

26. The composition of claim 16 , wherein the biological target-binding domain is the same for each of the plurality of capture probes.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2020
From: CHEE, MARK S.
To: PROGNOSYS BIOSCIENCES, INC.
Reel/Frame 053914/0655 →
Continuity (8)
Continuation 16988284 · Aug 7, 2020
Continuation 16414213 · May 16, 2019
Continuation 16402098 · May 2, 2019
Continuation 16276235 · Feb 14, 2019
Continuation 15187661 · Jun 20, 2016
Continuation 13080616 · Apr 5, 2011
Provisional Application 61321124 · Apr 5, 2010
Related Publication 20210002713A1 · Jan 7, 2021
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