CA2377567A1 - High throughput assay system - Google Patents

High throughput assay system Download PDF

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CA2377567A1
CA2377567A1 CA002377567A CA2377567A CA2377567A1 CA 2377567 A1 CA2377567 A1 CA 2377567A1 CA 002377567 A CA002377567 A CA 002377567A CA 2377567 A CA2377567 A CA 2377567A CA 2377567 A1 CA2377567 A1 CA 2377567A1
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target
detection
combination
sample
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CA2377567C (en
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Richard M. Kris
Stephen Felder
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813—Hybridisation assays
    • C12Q1/6834—Enzymatic or biochemical coupling of nucleic acids to a solid phase
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Abstract

The present invention relates to compositions, apparatus and methods useful for concurrently performing multiple, high throughput, biological or chemica l assays, using repeated arrays of probes. A combination of the invention comprises a surface, which comprises a plurality of test regions, at least t wo of which, and in a preferred embodiment, at least twenty of which, are substantially identical, wherein each of the test regions comprises an array of generic anchor molecules. The anchors are associated with bifunctional linker molecules, each containing a portion which is specific for at least o ne of the anchors and a portion which is a probe specific for a target of interest. The resulting array of probes is used to analyze the presence or test the activity of one or more target molecules which specifically interac t with the probes. In one embodiment of the invention, the test regions (which can be wells) are further subdivided into smaller subregions (indentations, or dimples).

Claims (49)

1. A method of detecting at least one target, comprising a) contacting a sample which may comprise said target(s) with a combination which comprises, before the addition of said sample, i) a surface, comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising ii) at least eight different oligonucleotide anchors, each in association with iii) a bifunctional linker which has a first portion that is specific for the oligonucleotide anchor, and a second portion that comprises a probe which is specific for said target(s).
wherein the target(s) is a protection fragment(s) and is amplified by PCR
before said sample(s) is contacted with said combination, under conditions effective for said target(s) to bind to said combination, b) contacting said combination and any bound targets with a labeled detection probe, and c) detecting said detection probe.
2. The method of claim 1, wherein said target(s) are amplified by PCR using two PCR
primers, either or both of which comprises a chemical modification which allows the primer to attach to a solid surface.
3. The method of claim 1, wherein said target(s) ace amplified by PCR using two PCR
primers, either or both of which comprises one or more restriction enzyme sites.
4. The method of claim 1, wherein said target(s) ate amplified by PCR using two PCR
primers, either or both of which comprises one or more peptide sequences which can be cleaved by a protease.
5. The method of claim 1, wherein said target(s) are amplified by PCR using two PCR
primers, either or both of which comprises a sequence which is specific for said detection probe.
6. A method of detecting at least one target, comprising a) contacting a sample which may comprise said target(s) with a combination which comprises, before the addition of said sample, i) a surface, comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising ii) at least eight different oligonucleotide anchors, each in association with iii) a bifunctional linker which has a first portion that is specific for the oligonucleotide anchor, and a second portion that comprises a probe which is specific for said target(s).
under conditions effective for said target(s) to bind to said combination, b) contacting said combination and any bound targets with a labeled detection probe, and c) detecting said detection probe, wherein said labeled detection probe comprises an upconverting phosphore
7. The method of claim 6, wherein said combination and any bound targets are contacted with at least two different labeled detection probes, each of which labeled probe comprises a different upconverting phosphore.
8. The method of claim 6, wherein said target(s) is a nuclease protection fragment.
9. The method of claim 8, wherein said combination and any bound targets are contacted with at least two labeled detection probes, each of which labeled probe comprises a different upconverting phosphore
10. A method of detecting at least one target, comprising a) contacting a sample which may comprise said target(s) with a combination which comprises, before the addition of said sample, i) a surface comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising ii) at least eight different oligonucleotide anchors, each in association with iii) a bifunctional linker which has a first portion that is specific for the oligonucleotide anchor, and a second portion that comprises a probe which is specific for said target(s), under conditions effective for said target(s) to bind to said combination, b) contacting said combination and any bound targets with a detection linker, which comprises a moiety specific for said target and a moiety specific for a reporter reagent, which interacts with said detection linker and which comprises a signaling entity, c) contacting said detection linker with said reporter reagent, and d) detecting said signaling entity.
11. The method of claim 10, wherein said target(s) is a nuclease protection fragment.
12. The method of claim 10, which is a method for detecting at least two targets, further comprising b) contacting said combination and any bound targets with at least two detection linkers, each of which comprises a moiety specific for one of said targets and a moiety specific for a common reporter reagent.

c) contacting said detection linkers with said common reporter reagent, which interacts with said detection linkers and which comprises a signaling entity, and d) detecting said signaling entity.
13. The method of claim 12, wherein said targets are nuclease protection fragments.
14. The method of claim 12, wherein said signaling entity comprises an upconverting phosphore.
15. A method of detecting at least two RNAs, comprising a) incubating a sample which may comprise said RNAs with two or more protection fragments under conditions which are effective for hybridization of said protection fragments to said RNAs, wherein each of said protection fragments comprises a common 3' overhanging sequence which is not specific for said RNAs.
b) subjecting said incubated sample to treatment with one or more nucleases effective for digesting nucleic acid other than the portion of said protection fragments which have hybridized to said RNAs and, optionally, the portions of said RNAs which have been hybridized, c) removing nucleic acid material other than said protection fragments which have hybridized to said RNAs, to provide a sample containing the protection fragments.
d) contacting said sample containing the protection fragments with a combination which comprises, before the addition of said sample, i) a surface, comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising ii) at least eight different oligonucleotide anchors, each in association with iii) a bifunctional linker which has a first portion that is specific for the oligonucleotide anchor, and a second portion that composes a probe which is specific for at least one of said protection fragments, under conditions effective for said protection fragments to bind to said combination, e) contacting said combination and any bound protection fragments with at least two detection linkers, each of which comprises a moiety specific for one of said protection fragments and a moiety specific for said common 3' overhanging sequence, f) contacting said detection linkers with a reporter reagent which is specific for said common reporter reagent and which comprises a signaling entity, and g) detecting said signaling entity.
16. The method of claim 15, wherein said signaling entity comprises an upconverting phosphore.
17. The method of claim 15, wherein one or more of said detection linkers is diluted with blocked detection linker.
18. A method of detecting at least one nucleic acid target, comprising a) contacting a sample which may comprise said target(s) with a nuclease protection fragment(s) specific for and which binds to said target(s), exposing the sample to a nuclease effective to digest remaining single strand nucleic acid, and then contacting the resultant sample with a combination winch comprises, before the addition of said sample, i) a surface, comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising ii) at least two different anchors, each in association with iii) a bifunctional linker which has 3 first portion that is specific for the anchor, and a second portion that comprises a probe which is specific for, said nuclease protection fragment(s), under conditions effective for said nuclease protection fragment(s) to bind to said combination, b) contacting said combination and any bound nuclease protection fragment(s) with at least one detection linker, which comprises a first moiety specific for one of said bound nuclease protection fragment(s) and a second moiety specific for a reporter reagent, and c) detecting said detection linker(s).
19. The method of claim 18, wherein said reporter reagent interacts with said detection linker(s) and comprises a signaling entity, further comprising d) contacting said detection linker(s) with said reporter reagent, and e) detecting said signaling entity.
20. The method of claim 18, wherein the anchors are oligonucleotide anchors.
21. A method of detecting at least two nucleic acid targets, comprising a) contacting a sample which may comprise said targets with nuclease protection fragments specific for and which bind to said targets, exposing the sample to a nuclease effective to digest remaining single strand nucleic acid, and then contacting the resultant sample with a combination which comprises, before the addition of said sample, i) a surface, comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising ii) at least two different anchors, each in association with iii) a bifunctional linker which has a first portion that is specific for the anchor, and a second portion that comprises a probe which is specific for one of said nuclease protection fragments, under conditions effective for said nuclease protection fragments to bind to said combination, b) contacting said combination and any bound nuclease protection fragments with at least two detection linkers, each of which comprises a first moiety specific for one of said nuclease protection fragments and a second moiety specific for a common reporter reagent, and c) detecting said detection linkers.
22. The method of claim 21, wherein said reporter reagent interacts with said detection linker(s) and comprises a signaling entity, further comprising d) contacting said detection linker(s) with said reporter reagent, and e) detecting said signaling entity.
23. The method of claim 21, wherein the anchors are oligonucleotide anchors.
24. A method of detecting at least two nucleic acid targets of interest in a sample which may comprise said targets, comprising a) incubating said sample with two or more protection fragments under conditions which arc effective for hybridization of said protection fragments to said nucleic acids of interest in said sample, wherein each of said protection fragments comprises a common 3' overhanging sequence which is not specific for said nucleic acids of interest, b) subjecting said incubated sample to treatment with one or more nucleases effective for digesting nucleic acid other than the portions of said protection fragments which have hybridized to the nucleic acids of interest and, optionally, the portions of said nucleic acids of interest which have been hybridized, c) removing nucleic acid material other than said protection fragments which have hybridized to said nucleic acids of interest, to provide a sample containing the protection fragments, then d) contacting said sample containing the protection fragments with a combination which comprises, before the addition of said sample, i) a surface, comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising ii) at least two different anchors, each in association with iii) a bifunctional linker which has s first portion that is specific for the anchor, and a second portion that comprises a probe which is specific for one of said protection fragments, under conditions effective for said protection fragments to bind to said combination, and e) contacting said combination and any bound protection fragments with at least two detection linkers, each of which comprises a first moity specific for one of said protection fragments and a second moiety specific for said common 3' overhanging sequence.
25. The method of claim 24, further comprising f) contacting said detection linkers with a reporter reagent which is specific for said common 3' overhanging sequence and which comprises a signaling entity, and g) detecting said signaling entity.
26. The method of claim 24, wherein the anchors are oligonucleotide anchors.
27. The method of claim 26, wherein one or more of the detection linkers is diluted with blocked detection linker.
28. The method of claim 23, wherein at least one of said anchors is is association with a plurality of bifunctional linkers, each of which has a first portion that is specific for the anchor, and a second portion which comprises a probe which is specific for a different nuclease protection fragment.
29. The method of claim 18, wherein said anchors have been dissociated from bifunctional linkers having a different target specificity.
30. The method of claim 18, wherein said combination comprises a large number of said regions, and wherein the method is high throughput.
31. A kit useful for the detection of at least one nucleic acid target in a sample, which comprises a) at least one nuclease protection fragment specific for at least one of said targets, but not for any of the oligonucleotide anchors in said kit.

b) a surface, comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising at least two different oligonucleotide anchors, c) a container comprising at least one bifunctional linker molecule, which has a first portion specific for at least one of said oligonucleotide anchors and a second portion that comprises a probe which is specific for, and in said detection binds to, at least one of said nuclease protection fragments, and d) at least one detection linker, which has a first moiety specific for one of said nuclease protection fragments and a second moiety specific for a reporter reagent.
32. A kit useful for the detection of at least one nucleic acid target in a sample, which comprises.

a) at least one nuclease protection fragment specific for at lest one of said targets, but not for any of the other oligonucleotides in said kit, b) at least one bifunctional linker which has a first portion that is specific for an oligonucleotide anchor, and a second portion which is specific for, and is said detection binds to, at least one of said nuclease protection fragments, and c) at least one detection linker, which has a first moiety specific for one of said nuclease protection fragments and a second moiety specific for a reporter reagent.
33. The method of claim 18, wherein each region comprises at least eight different anchors.
34. The method of claim 21, wherein each region comprises at least eight different anchors.
35. The method of claim 24, wherein each region comprises at least eight different anchors.
36. A method of detecting at least one nucleic acid target, comprising a) contracting a sample which may comprise said target(s) with a nuclease protection fragment(s) specific for and which binds to said target(s) and exposing the resultant product to a nuclease effective to digest single strand nucleic acid, and then contacting the resultant sample with a combination which comprises, before the addition of said sample, i) a surface comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising ii) at least two different anchors, each in association with iii) a bifunctional linker which has a first portion that is specific for the anchor.
and a second portion that comprises a probe which is specific for portions of said nucleic acid target(s) which are protected by said nuclease protection fragment, under conditions effective for said protected portions(s) to bind to said combination, b) contacting said combination and any bound protected portion(s) with at least one detection linker, which comprises a first moiety specific for one of said bound protected portion (s) and a second moiety specific for a reporter reagent, and c) detecting said detection linker
37. The method of claim 36, wherein said reporter reagent interacts with said detection linker(s) and comprises a signaling entity, further comprising d) contacting said detection linker(s) with said reporter reagent, and e) detecting said signaling entity.
38. The method of claim 36, wherein each region comprises at least eight different anchors.
39. A method of detecting at least one target, comprising a) contacting a sample which may comprise said target(s) with a combination which comprises, before the addition of said sample, i) a surface, comprising multiple spatially discrete regions, at least two of which ace substantially identical, each region comprising ii) at least two different loci of anchors, the anchors at each locus each is association with iii) a bifunctional linker which has a first portion that is specific for the anchor, and a second portion that comprises a probe which is specific for said target(s), under conditions effective for said target(s) to bind to said combination, and wherein two or more of the anchors located at at least one locus of a region are in association with different bifunctional linkers, having different target specificities.
40. The method of claim 39, further comprising b) contacting said combination and any bound targets with at least one detection linker, which comprises a first moiety specific for one of said bound target(s) and a second moiety specific for a reporter reagent.
41. The method of claim 39, further comprising c) contacting said combination and any behind targets with at least one detection probe.
42. The method of claim 41, wherein a first detection probe binds to a first target bound to the combination at a first locus, a second detection probe binds to a second target bound to the combination at the same locus, and the first and second detection probes are detected simultaneously or sequentially.
43. The method of claim 39, wherein said target(s) is a nuclease protection fragment(s) specific for a nucleic acid(s) of interest.
44. The method of claim 40, wherein said target(s) is a nuclease protection fragment(s) specific for a nucleic acid(s) of interest.
45. The method of claim 42, wherein said target(s) is a nuclease protection fragment(s) specific for a nucleic acid(s) of interest.
46. The method of claim 39, wherein each region comprises at least eight different anchors
47. The kit of claim 31, wherein tech region comprises at least night different anchors.
48. The kit of claim 31, further comprising e) one or more nucleases effective for digesting single strand nucleic acid and/or the RNA strand of a DNA/RNA duplex.
49. A kit useful for the detection of at least one nucleic acid target, comprising a) at least one nuclease protection fragment specific for said target(s), but not for any of the oligonucleotide anchors in said kit, b) a surface, comprising multiple spatially discrete regions, at least two of which are substantially identical, each region comprising at least two different oligonucleotide anchors, c) a container comprising at least one bifunctional linker molecule, which has a first portion specific for at least one of said oligonucleotide anchors and a second portion that comprises a probe which is specific for, and in said detection binds to, at feast one of said nuclease protection fragments, d) at least ant detection linker, which has a first moiety specific for one of said nuclease protection fragments and a second moiety specific for a reporter reagent, and r) one or more nucleases effective for digesting single strand nucleic acid and/or the RNA strand of a DNA/RNA duplex.
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