Reagents and methods for improving reproducibility and reducing mispriming in PCR amplification

• US 7,517,977 B2
• Filed: 10/17/2005
• Issued: 04/14/2009
• Est. Priority Date: 10/18/2004
• Status: Active Grant

• Current Assignee: Brandeis University
• Original Assignee: Brandeis University
• Inventors: Rice, John, Pierce, Kenneth, Reis, Arthur, Wangh, Lawrence J., Salk, Jesse, Hartshorn, Cristina, Sanchez, J. Aquiles
• Primary Examiner(s): Kim; Young J
• Application Number:
  US11/252,506
• Publication Number:
  US 20060177842A1
• Time in Patent Office: 1,275 Days
• Field of Search: None
• US Class Current: 536/24.3
• CPC Class Codes: C12Q 1/6848 characterised by the means for preventing contamination or increasing the specificity or sensitivity of an amplification reaction
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 2525/186 incorporating a non-extendable or blocking moiety
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2527/125 Specific component of sample, medium or buffer
• CPC Class Codes: C12Q 2527/137 Concentration of a component of medium
• CPC Class Codes: C12Q 2531/107 Probe or oligonucleotide ligation

Abstract

An additive for preventing mispriming in polymerase chain reaction (PCR) amplifications and assays comprising a hairpin oligonucleotide having a stem duplex greater than six nucleotides in length and a stabilized stem terminus. The additive improves PCR amplifications, including LATE-PCR amplifications when added to initial amplification reaction mixtures. It can be included in oligonucleotide sets and in kits for PCR amplification and assays.

Claims

1. A reagent capable of preventing at least one manifestation of mispriming in a polymerase chain reaction (PCR) amplification to produce at least one amplified DNA product when added at a concentration of not more than 650 nM to a PCR amplification mixture that includes 1.25 units of a thermostable DNA polymerase per 25 pA of reaction mixture, said reagent being an oligonucleotide that has a 3′

end and a stem-loop structure having a stem comprising a double-stranded region that has a length is greater than six nucleotides and a terminus away from the loop comprising a 3′

nucleotide and a 5′

nucleotide, said stem having a calculated stem melting temperature (Tm) below 94°

C.,

wherein

a) the 3′

end is non-extendable by said DNA polymerase,

b) the oligonucleotide is not fluorescently labeled and does not contribute background fluorescence, and

c) said stem terminus is stabilized by means selected from the group consisting of non-fluorescent fluorophore-iuenching moieties covalently attached to the 3′ and

5′

nucleotides of said stem terminus and pairs of non-natural nucleotides that bind more strongly than a natural DNA-DNA hybrid and that include each of the 3′ and

5′

nucleotides of said stem terminus.

2. The reagent according to claim 1, wherein the stem-stabilization means are non-fluorescent fluorophore-quenching moieties.

3. The reagent according to claim 1, wherein the loop is selected from the group consisting of an oligonucleotide comprising at least three nucleotides and a non-nucleotide chemical linker.

4. The reagent according to claim 3, wherein the chemical linker is a methylene bridge of 3-6 carbon atoms.

5. The reagent according to claim 1, wherein the stem comprises a double-stranded region of 9-12 base pairs.

6. The reagent according to claim 5, wherein the stem is blunt ended and contains no internal mismatches.

7. The reagent according to claim 1, wherein the stem has a calculated melting temperature (Tm) in a range selected from the group consisting of 72-85°

C. and 50-71°

C.

8. The reagent according to claim 7, wherein the stem-stabilization means are non-fluorescent fluorophore-quenching moieties.

9. The reagent according to claim 1, wherein the stem-stabilization means are pairs of 2′

-O-methyl nucleotides.

10. The reagent according to claim 9, wherein the loop is selected from the group consisting of an oligonucleotide comprising at least three nucleotides and a non-nucleotide chemical linker.

11. The reagent according to claim 9, wherein the stem comprises a double-stranded region of 9-12 base pairs.

12. A set of oligonucleotides for performing a polymerase chain reaction (PCR) amplification comprising at least one pair of PCR primers and at least one reagent according to claim 1.

13. The set according to claim 12, further comprising at least one fluorescently labeled probe that hybridizes to the amplified product defined by said at least one pair of PCR primers.

14. The set according to claim 12, wherein the stem-stabilizing means are non-fluorescent fluorophore-quenching moieties.

15. A kit of reagents for performing a polymerase chain reaction (PCR) amplification comprising a thermostable DNA polymerase, at least one pair of PCR primers, dNTPs and at least one mispriming prevention reagent according to claim 1.

16. The kit according to claim 15, further comprising reagents for nucleic acid isolation.

17. The kit according to claim 15, wherein the mispriming prevention reagent has a stem comprising a double-stranded sequence of 9-12 nucleotides.

18. The kit according to claim 15, wherein the stem-stabilization means are non-fluorescent fluorophore-quenching moieties.

19. The kit according to claim 15, wherein the mispriming prevention reagent has a stem with a calculated melting temperature (Tm) in a range selected form the group consisting of 72-85°

C. and 50-71°

C.