Nucleic acid amplification and detection methods using rapid polymerase chain reaction cycle

• US 6,475,729 B1
• Filed: 10/29/1999
• Issued: 11/05/2002
• Est. Priority Date: 04/30/1991
• Status: Expired due to Fees

• Current Assignee: Johnson & Johnson Clinical Diagnostics Inc. (Johnson & Johnson)
• Original Assignee: Johnson & Johnson Clinical Diagnostics Inc. (Johnson & Johnson)
• Inventors: Backus, John Wesley, Findley, John Bruce, Sutherland, John William H., Donish, William Harold
• Primary Examiner(s): Arthur, Lisa B.
• Application Number:
  US09/430,256
• Time in Patent Office: 1,103 Days
• Field of Search: 435/91.2, 435/6
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 1/703 Viruses associated with AIDS
• CPC Class Codes: C12Q 2527/107 Temperature of melting, i.e. Tm
• CPC Class Codes: C12Q 2527/113 Time
• CPC Class Codes: C12Q 2527/143 Concentration of primer or probe
• CPC Class Codes: C12Q 2527/149 Concentration of an enzyme

Abstract

Nucleic acids can be amplified and detected using a very rapid polymerase chain reaction procedure. This procedure includes a series of steps which have critically defined temperature and time parameters. Each polymerase chain reaction cycle requires generally less than about two minutes, and in most cases less than 90 seconds. At least 5 units/100 μl of solution of thermostable DNA polymerase are used, and other preferred levels of primer concentrations facilitate the quick cycling in the amplification. In preferred embodiments, only two temperatures are used in the amplification.

Claims

1. A method for the amplification of a nucleic acid comprising the steps of:

A. heating a targeted double-stranded nucleic acid at a first temperature of about 85 to about 100°

C. for about 1 to about 40 seconds to denature the strands of said nucleic acid,

B. cooling said denatured strands to a second temperature over a time period of about 5 to about 20 seconds,

C. in the presence of

1) a thermostable DNA polymerase present in an amount of at least 5 units/100 microliters of solution,

2) deoxyribonucleoside-5′

-triphosphates present in amounts effective for DNA polymerization, and

3) a set of primers specific for said denatured strands, said primers being present in amounts effective for DNA polymerization,

forming hybridized primer extension products of said primers and denatured strands by incubating said denatured strands at said second temperature for about 1 to about 80 seconds,

said second temperature being in the range of about (T_m−

15)°

C. to about (T_m+5)°

C. wherein T_m is the melting temperature of said denatured strands and said primers, and the difference Δ

T between said first and second temperatures being from about 5 to about 45°

C.,

D. heating said hybridized primer extension products to said first temperature over a period of time of about 5 to about 20 seconds and keeping said products at said temperature for about 1 to about 40 seconds, and

E. repeating steps B through D sequentially as a cycle at least once wherein each cycle of steps B through D is carried out within about 20 to about 120 seconds, provided that if the concentration of each of said primers is less than about 0.075 micromolar the time for each cycle of Steps B through D is at least about 60 seconds.

2. The method of claim 1 wherein heating step A is carried out at a temperature of from about 90 to about 98°

C. for from about 1 to about 20 seconds.

3. The method of claim 1 wherein step D is carried out at a temperature of from about 90 to about 98°

C., and the time for heating to said temperature is from about 5 to about 10 seconds, and the time of maintaining said temperature is from about 1 to about 15 seconds.

4. The method of claim 1 wherein the second temperature is from about 55 to about 70°

C., and step B is carried out for a time of from about 5 to about 15 seconds.

5. The method of claim 1 wherein said second temperature is from about 55 to about 70°

C., and step C is carried out for from about 1 to about 40 seconds.

6. The method of claim 1 wherein said DNA polymerase is a thermostable DNA polymerase isolated from a Thermus species or from a genetically engineered equivalent thereof.

7. The method of claim 6 wherein said polymerase is isolated from Thermus aquaticus, Thermus thermophilus or Thermus flavus, or a genetically engineered equivalent thereof.

8. The method of claim 1 further comprising detection of said primer extension products after step C is performed the last time, either in denatured or undenatured form.

9. The method of claim 1 wherein each cycle of steps B through D is carried out within from about 20 to about 90 seconds.

10. The method of claim 1 wherein each cycle of steps B through D is carried out within from about 30 to about 75 seconds.

11. The method of claim 1 wherein said thermostable DNA polymerase is present at concentration of from about 6 to about 20 units/100 μ

l of solution.

12. The method of claim 1 wherein the targeted nucleic acid and the reagents of step C are mixed in a volume of from about 50 to about 300 μ

l.

13. The method of claim 1 wherein Δ

T is from about 20 to about 35°

C.

14. The method of claim 1 wherein Δ

T is from about 15 to about 45°

C.

15. The method of claim 1 wherein the concentration of each primer is from about 0.1 to about 2 μ

molar.

28. The method of claim 1 which is carried out in a chemical test pack.

29. The method of claim 1 which is carried out in a reaction tube.

16. A method for the amplification and detection of a nucleic acid comprising the steps of:

A. heating a targeted double-stranded nucleic acid at a first temperature of about 85 to about 100°

C. for about 1 to about 40 seconds to denature the strands of said nucleic acid,

B. cooling said denatured strands to a second temperature over a time period of about 5 to about 20 seconds,

C. in the presence of

1) a thermostable DNA polymerase present in an amount of at least 5 units/100 microliters of solution,

2) deoxyribonucleoside-5′

-triphosphates present in amounts effective for DNA polymerization, and

3) a set of primers specific for said denatured strands, said primers being present in amounts effective for DNA polymerization,

forming hybridized primer extension products of said primers and denatured strands by incubating said denatured strands at said second temperature for about 1 to about 80 seconds,

said second temperature being in the range of about (T_m−

15)°

C. to about (T_m+5)°

C. wherein T_m is the melting temperature of said denatured strands and said primers, and the difference Δ

T between said first and second temperatures being from about 5 to about 45°

C.,

D. heating said hybridized primer extension products to said first temperature over a period of time of about 5 to about 20 seconds and keeping said products at said temperature for from about 1 to about 40 seconds, and

E. repeating steps B through D sequentially as a cycle at least once wherein each cycle of steps B through D is carried out within about 20 to about 120 seconds,

F. detecting at least one denatured strand of said nucleic acid, provided that if the concentration of each of said primers is less than about 0.075 micromolar the time for each cycle of Steps B through D is at least about 60 seconds.

17. The method of claim 16 wherein one of said primers is biotinylated, and said detection in step F is carried out by capturing the resulting amplified biotinylated strand using avidin which is attached to a solid substrate, and detecting said captured strand directly or indirectly with a labeled probe.

18. The method of claim 16 wherein one of said primers is biotinylated, and detection in step F is carried out by capturing the resulting amplified biotinylated strand using an insolubilized oligonucleotide complementary thereto, and complexing said biotinylated strand with detectably labeled avidin.

19. The method of claim 16 for the amplification and detection of genomic, bacterial, fungal or viral DNA.

20. The method of claim 19 for the amplification and detection of viral or bacterial DNA.

21. The method of claim 16 for the amplification and detection of viral DNA.

22. The method of claim 21 for the amplification and detection of HIV-I DNA, cytomegaloviral DNA or human papilloma viral DNA.

23. The method of claim 16 for the simultaneous amplification and detection of a plurality of double-stranded nucleic acids using corresponding sets of primers.

24. The method of claim 16 wherein detection in step F is carried out by capturing said denatured strand on a microporous filtration membrane.

25. The method of claim 16 wherein detection in step F is carried out by capturing said denatured strand on a nonporous substrate selected from the group consisting of a polymeric film, a noncoated paper and a polymer coated paper.

26. The method of claim 16 wherein detection is carried out using polymeric particles for insolubilizing said denatured strand.

27. The method of claim 26 wherein each cycle of Steps B through D is carried out within about 30 to about 75 seconds.