Method for polymerase chain reactions with use of a DNA polymerase with proofreading properties

Patent metadata

Field	Value
Publication number	US-9309567-B2
Application number	US-54049206-A
Country	US
Kind code	B2
Filing date	Sep 28, 2006
Priority date	Oct 5, 2005
Publication date	Apr 12, 2016
Grant date	Apr 12, 2016

Abstract

The present invention concerns a method for a polymerase chain reaction, in which a template nucleic acid, at least one primer, deoxyribonucleoside triphosphates as well as a DNA polymerase with proofreading activity are used. In addition, according to this invention, at least one target substrate is added to the polymerase chain reaction, whereby the efficiency of the DNA polymerase with proofreading activity is significantly increased. Any molecule that reduces or, in the optimal case, blocks the 3′,5′-exonuclease activity of the DNA polymerase used is suitable as target substrate. Technical solutions for the added substrate (target substrate) are in particular single stranded, linear oligonucleotides, hairpin oligonucleotides and RNA and DNA molecules. Furthermore, a kit is disclosed which comprise the required reagents for the implementation of the method according to the invention.

First claim

The invention claimed is:

1. A method for nucleic acid amplification, comprising amplifying a nucleic acid via performing a polymerase chain reaction (PCR) in the presence of (i) a DNA template, (ii) a DNA polymerase with proofreading activity, (iii) at least one primer, (iv) deoxyribonucleoside triphosphates, and (v) at least one target substrate,
wherein the at least one primer is not resistant to degradation by the proofreading activity of the DNA polymerase,
wherein the at least one target substrate
(a) is a single stranded oligonucleotide in which at least one phosphate in the backbone of said single stranded oligonucleotide is replaced by at least one phosphorothioate,
(b) is modified at its 3′-end so that it is incapable of being elongated by the DNA polymerase with proofreading activity,
(c) has a random sequence,
(d) forms a double stranded nucleic acid molecule with a strand of the DNA template under PCR conditions, and
(e) is able as the double stranded nucleic acid molecule of (d) to serve as a binding site for the polymerase with proofreading activity, thereby reducing the 3′-exonuclease activity of the DNA polymerase toward the primer or the DNA template, and

wherein the molecular ratio of the polymerase with proofreading activity to the at least one target substrate is between 1:1 and 1:1000.

2. The method according to claim 1 , wherein the OH group at the 3′-end of the single stranded oligonucleotide is replaced with a phosphate group or another residue, or the single stranded oligonucleotide comprises a dideoxynucleotide, one or several inverse bases, RNA, an abasic site, a spacer, a dye, a quencher residue, or a modified base at its 3′-end.

3. The method according to claim 1 , wherein the single stranded oligonucleotide has a length of 10 to 100 bases.

4. The method according to claim 1 , wherein the single stranded oligonucleotide is present in the polymerase chain reaction in a concentration of 0.1 to 20 μM.

5. The method of claim 1 , wherein the at least one target substrate forms a double stranded nucleic acid molecule with a strand of the DNA template during the annealing stage of the polymerase chain reaction.

6. The method of claim 5 , wherein the annealing is carried out at a temperature between 40 and 70° C.

7. The method of claim 1 , wherein at least the phosphate in the backbone of the single stranded oligonucleotide on the 3′-end between the last and penultimate bases is replaced by a phosphorothioate.

8. The method of claim 1 , wherein the at least one target substrate is the oligonucleotide as set forth in SEQ ID NO: 22 in which the phosphate in the backbone on the 3′-end between the last and penultimate bases is replaced by a phosphorothioate, and the 3′-OH group is replaced with a 3′-phosphate group.

9. The method of claim 1 , wherein the single stranded oligonucleotide has a length of 12 to 80 bases.

10. The method of claim 1 , wherein the single stranded oligonucleotide has a length of 20 to 45 bases.

11. The method of claim 1 , wherein the molecular ratio of the polymerase with proofreading activity to the single stranded oligonucleotide is between 1:1 and 1:500.

12. The method of claim 1 , wherein the molecular ratio of the polymerase with proofreading activity to the single stranded oligonucleotide is between 1:1 and 1:200.

Assignees

• Engel Holger
• Peist Ralf
• Qiagen Gmbh

Inventors

• Engel Holger
• Peist Ralf

Classifications

• C12Q2525/179

  incorporating arbitrary or random nucleotide sequences · CPC title

• C12Q2521/101

  DNA polymerase · CPC title

• C12Q2525/186

  incorporating a non-extendable or blocking moiety · CPC title

• C12Q2527/125

  Specific component of sample, medium or buffer · CPC title

• C12Q2525/113

  incorporating modified backbone · CPC title