PCR hot start using primers with the structure of molecular beacons (hairpin-like structure)
Open Access
- 1 November 2000
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 28 (21) , 94e-94
- https://doi.org/10.1093/nar/28.21.e94
Abstract
A new technique of PCR hot start using oligonucleotide primers with a stem-loop structure is developed here. The molecular beacon oligonucleotide structure without any chromophore addition to the ends was used. The 3'-end sequence of the primers was complementary to the target and five or six nucleotides complementary to the 3'-end were added to the 5'-end. During preparation of the reaction mixture and initial heating, the oligonucleotide has a stem-loop structure and cannot serve as an effective primer for DNA polymerase. After heating to the annealing temperature it acquires a linear structure and primer extension can begin.Keywords
This publication has 11 references indexed in Scilit:
- Thermodynamic basis of the enhanced specificity of structured DNA probesProceedings of the National Academy of Sciences, 1999
- [Hot start of the polymerase chain reaction using DNA helicase].1999
- Molecular beacon sequence analysis for detecting drug resistance in Mycobacterium tuberculosisNature Biotechnology, 1998
- Oligonucleotide Inhibitors ofTaqDNA Polymerase Facilitate Detection of Low Copy Number Targets by PCRJournal of Molecular Biology, 1996
- Molecular Beacons: Probes that Fluoresce upon HybridizationNature Biotechnology, 1996
- AmpliGrease: "hot start" PCR using petroleum jelly.1994
- Automated "hot start" PCR using mineral oil and paraffin wax.1993
- Maximizing sensitivity and specificity of PCR by preamplification heatingNucleic Acids Research, 1991
- IS6110, an IS-like element ofMycobacterium tuberculosiscomplexNucleic Acids Research, 1990
- Characterization of the human p53 gene.Molecular and Cellular Biology, 1986