Polynucleotide capture assay employing in vitro amplification

• US 5,200,314 A
• Filed: 03/23/1990
• Issued: 04/06/1993
• Est. Priority Date: 03/23/1990
• Status: Expired due to Term

• Current Assignee: Siemens Healthcare Diagnostics Incorporated (Siemens AG)
• Original Assignee: Chiron Corporation (Novartis Ag)
• Inventors: Urdea, Michael
• Primary Examiner(s): Wax, Robert A.
• Assistant Examiner(s): Escallon, Miguel
• Application Number:
  US07/497,938
• Time in Patent Office: 1,110 Days
• Field of Search: 435/6, 435/91, 435/810, 536/27, 536/5, 935/78, 935/77, 436/501, 436/94
• US Class Current: 435/6.17
• CPC Class Codes: C12Q 1/6813 Hybridisation assays
• CPC Class Codes: C12Q 1/682 Signal amplification
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 1/706 for hepatitis
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10T 436/143333 Saccharide [e.g., DNA, etc.]

Abstract

An analyte polynucleotide strand having an analyte sequence is detected within a sample containing polynucleotides by contacting the analyte polynucleotide with a capture probe under hybridization conditions, where the capture probe has a first binding partner specific for a solid-phase second binding partner. The resulting duplex is then immobilized by specific binding between the binding partners, and non-bound polynucleotides are separated from the bound species. The analyte polynucleotide is optionally displaced from the solid phase, then amplified by PCR. The PCR primers each have a polynucleotide region capable of hybridizing to a region of the analyte polynucleotide, and at least one of the primers further has an additional binding partner capable of binding a solid-phase binding partner. The amplified product is then separated from the reaction mixture by specific binding between the binding partners, and the amplified product is detected.

Claims

1. A method for detecting an analyte polynucleotide strand having an analyte sequence within a sample containing polynucleotides, which method comprises:

a) contacting said analyte polynucleotide with a capture probe under hybridization conditions to form an analyte-capture probe complex, said capture probe comprising an analyte-binding region and a first specific binding partner, said analyte-binding region hybridizable with a region of said analyte polynucleotide, and said first specific binding partner having specificity for a second binding partner;

b) contacting said first specific binding partner with said second binding partner, wherein said second binding partner is immobilized on a first support, whereby said analyte-capture probe complex is immobilized at said first support to provide an immobilized analyte-capture probe complex;

c) separating nonbound polynucleotides from said immobilized analyte-capture probe complex;

d) contacting said analyte polynucleotide with a first primer complementary to a first primer-binding region of said analyte polynucleotide under hybridizing conditions, said first primer comprising an analyte-hybridizing region and a third specific binding partner separated from one another by means for halting transcription therebetween;

e) initiating nucleotide polymerization with polymerization means at said first primer to form an analyte-complementary strand duplex said complementary strand complementary to said analyte but not to said third specific binding partner;

f) denaturing said analyte-complementary strand duplex to yield said complementary strand separated from said analyte polynucleotide;

g) contacting said complementary strand with a second primer capable of hybridizing to a second primer-binding region of said complementary strand, and contacting said analyte polynucleotide with said first primer;

h) initiating nucleotide polymerization with polymerization means to form an analyte-copy duplex having a strand complementary to a region of said complementary strand containing said first primer-binding region, and an analyte-complementary strand duplex;

i) repeating steps f-h using the product of step h in place of the analyte-complementary strand duplex of step e to provide an amplified product comprising said first and second primers, amplified amounts of said analyte polynucleotide and a polynucleotide sequence complementary to said analyte sequence; and

j) detecting said amplified product.

2. The method of claim 1, wherein said first specific binding partner comprises a first polynucleotide strand having a sequence which is not complementary to said analyte, polynucleotide said second binding partner comprises a second polynucleotide strand having a sequence which is complementary to said first binding partner polynucleotide strand and is not complementary to said analyte polynucleotide and wherein the means for halting transcription in said first primer is an arresting linker.

3. The method of claim 2, wherein said analyte polynucleotide is displaced from said first support by hybridizing to said second binding partner polynucleotide strand a displacing polynucleotide strand having a region complementary to said second binding partner polynucleotide strand.

4. The method of claim 2, wherein said analyte polynucleotide is displaced from said first support by hybridizing to said first binding partner polynucleotide strand a displacing polynucleotide strand having a region complementary to said first binding partner polynucleotide strand.

5. The method of claim 1, wherein said first primer further comprises at its 3'"'"' end a third binding partner, said third binding partner specifically binding to a fourth binding partner, wherein said fourth binding partner is bound to a solid support and wherein the means for halting transcription in said first primer is an arresting linker.

6. The method of claim 5, wherein said detecting step comprises:

contacting said amplified product with a solid support having said fourth binding partner bound thereto, and hybridizing said third binding partner to said fourth binding partner, to provide an immobilized amplified product;

separating non-bound polynucleotides from said immobilized amplified product; and

detecting the presence of said amplified product.

7. The method of claim 6 wherein said third binding partner comprises a third polynucleotide strand having a sequence which is not complementary to said analyte polynucleotide coupled to said primer by an arresting linker, and said fourth binding partner comprises a fourth polynucleotide strand having a sequence which is complementary to said third binding partner polynucleotide strand and is not complementary to said analyte polynucleotide.

8. The method of claim 6 wherein said second primer further comprises a fifth specific binding partner at its 3'"'"' end coupled to said primer by an arresting linker, capable of specifically binding to a sixth binding partner, wherein said sixth binding partner is bound to a detectable label.

9. The method of claim 8, wherein said detecting step further comprises:

contacting said immobilized amplified product with said labeled sixth binding partner;

separating non-bound sixth binding partner; and

determining the presence of bound sixth binding partner.

10. The method of claim 8 wherein said fifth binding partner comprises a fifth polynucleotide strand having a sequence which is not complementary to said analyte strand, and said sixth binding partner comprises a sixth polynucleotide strand having a sequence which is complementary to said fifth binding partner polynucleotide strand and it not complementary to said analyte polynucleotide or said analyte-complementary strand.

11. The method of claim 1, wherein said second primer further comprises at its 3'"'"' end a third binding partner coupled to said primer by an arresting linker, wherein said third binding partner is capable of specifically binding a fourth binding partner, wherein said fourth binding partner is bound to a support.

12. The method of claim 11, wherein said detecting step comprises:

contacting said amplified product with a solid support having said fourth binding partner bound thereto, and hybridizing said third binding partner to said fourth binding partner, to provide an immobilized amplified product;

separating non-bound polynucleotides from said immobilized amplified product; and

detecting the presence of said amplified product.

13. The method of claim 11 wherein said third binding partner comprises a third polynucleotide strand having a sequence which is not complementary to said analyte strand, and said fourth binding partner comprises a fourth polynucleotide strand having a sequence which is complementary to said third binding partner polynucleotide strand and is not complementary to said analyte polynucleotide or said analyte-complementary strand.

14. The method of claim 11 wherein said first primer further comprises a fifth specific binding partner at its 3'"'"' end, coupled to said primer by an arresting linker, wherein said fifth specific binding partner is capable of specifically binding to a sixth binding partner, wherein said sixth binding partner is bound to a detectable label.

15. The method of claim 14, wherein said detecting step comprises:

contacting said immobilized amplified product with said labeled sixth binding partner;

separating non-bound sixth binding partner; and

determining the presence of bound sixth binding partner.

16. The method of claim 14 wherein said fifth binding partner comprises a fifth polynucleotide strand having a sequence which is not complementary to said analyte strand, and said sixth binding partner comprises a sixth polynucleotide strand having a sequence which is complementary to said fifth binding partner polynucleotide strand and is not complementary to said analyte polynucleotide or said analyte-complementary strand.

17. The method of claim 1, which further comprises amplifying said analyte polynucleotide with third and fourth primers prior to contacting said analyte polynucleotide with said first primer, wherein said third and fourth primers hybridize to regions of said analyte polynucleotide and the complement of said analyte polynucleotide outside the region bounded by said first primer-binding region bounded by said first primer-binding region and second primer-binding region, thus amplifying the portion of the analyte polynucleotide and its complement which contains the analyte sequence and the first and second primer-binding regions.

18. An assay kit for amplifying and detecting an analyte polynucleotide strand having an analyte sequence within a sample containing polynucleotides, which kit comprises a package for:

a capture probe, said capture probe comprising an analyte-binding sequence complementary to a region of said analyte polynucleotide coupled to a displaceable first specific binding partner;

a first support, having bound thereto a second binding partner specific for said first partner;

a first primer complementary to a first primer-binding region of said analyte polynucleotide; and

a second primer complementary to a second primer-binding region of said analyte-complementary strand, wherein said second primer-binding region does not substantially overlap said first primer-binding region and wherein said first binding partner comprises a first polynucleotide strand having a sequence which is not complementary to said analyte strand coupled to said primer by an arresting linker, and said second binding partner comprises a second polynucleotide strand having a sequence which is complementary to said first binding partner polynucleotide strand and is not complementary to said analyte strand.

19. The assay kit of claim 18, which further comprises a displacing polynucleotide having a region complementary to said second binding partner polynucleotide.

20. The assay kit of claim 18, wherein said first primer further comprises at its 3'"'"' end a third binding partner capable of specifically binding a fourth binding partner coupled to said primer by an arresting linker, and

wherein said kit further comprises a support having said fourth binding partner bound thereto.

21. The assay kit of claim 20, wherein said second primer further comprises a fifth specific binding partner at its 3'"'"' end coupled to said primer by an arresting linker, capable of specifically binding to a sixth binding partner, and

wherein said kit further comprises a sixth binding partner bound to a detectable label.

22. The assay kit of claim 18, wherein said second primer further comprises at its 3'"'"' end a third binding partner coupled to said primer by an arresting linker, wherein said third binding partner is capable of specifically binding a fourth binding partner, and

wherein said kit further comprises a second support having said fourth binding partner bound thereto.

23. The assay kit of claim 22, wherein said first primer further comprises a fifth specific binding partner coupled to said primer by an arresting linker, wherein said fifth specific binding partner is capable of specifically binding a sixth binding partner, and

wherein said kit further comprises a sixth binding partner bound to a detectable label.

24. The assay kit of claim 18, which further comprises third and fourth primers complementary to said analyte polynucleotide and the complement thereof, wherein said third and fourth primers hybridize to regions of the analyte polynucleotide and its complement which are outside the region bounded by said first primer-binding region and second primer-binding region.