Kaboev O K, Luchkina L A, Tret'iakov A N, Bahrmand A R
St Petersburg Nuclear Physics Institute, Russian Academy of Science, Gatchina 188350, Russia and Tehran Pasteur Institute, Iran.
Nucleic Acids Res. 2000 Nov 1;28(21):E94. doi: 10.1093/nar/28.21.e94.
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.
本文开发了一种使用具有茎环结构的寡核苷酸引物进行PCR热启动的新技术。使用了末端未添加任何发色团的分子信标寡核苷酸结构。引物的3'-末端序列与靶标互补,并在5'-末端添加了与3'-末端互补的五个或六个核苷酸。在反应混合物制备和初始加热过程中,寡核苷酸具有茎环结构,不能作为DNA聚合酶的有效引物。加热至退火温度后,它获得线性结构,引物延伸可以开始。