Chang Yu-Hsuan, Wu Meng-Wei, Chen Yi-Ju, Vu Cao-An, Hong Ching-Ya, Chen Wen-Yih
Department of Chemical and Materials Engineering, National Central University, Jhongli, Taiwan.
Methods Mol Biol. 2022;2392:261-273. doi: 10.1007/978-1-0716-1799-1_18.
This chapter introduces neutralized DNA (nDNA) as a novel design for the primers of PCR and RT-PCR by methylating phosphate groups of some oligonucleotides in their structures. It starts with an introduction of the nDNA which possesses an electrically chimeric neutral backbone as well as the proposed standards in designing nDNA as a novel primer for PCR and RT-PCR , concluded from various experimental results presented afterward. The primary content comprises empirical data from PCR to compare nDNA and unmodified DNA as primers in terms of ability to distinguish and amplify mismatch templates, activities of polymerase enzymes, melting temperature of double-stranded sequences, and the trials and discussions on various modified positions of the nDNA primers. In summary, nDNA exhibited outstanding performance as a primer for PCR and RT-PCR , compared to unmodified DNA, and is expected to be expanded in diverse applications which require enhanced specificity.
本章介绍了一种通过甲基化某些寡核苷酸结构中的磷酸基团,将其作为PCR和RT-PCR引物的新型设计——中和DNA(nDNA)。首先介绍了具有电嵌合中性骨架的nDNA,以及根据随后给出的各种实验结果得出的将nDNA设计为PCR和RT-PCR新型引物的建议标准。主要内容包括来自PCR的实验数据,用于比较nDNA和未修饰DNA作为引物在区分和扩增错配模板的能力、聚合酶活性、双链序列的解链温度方面的差异,以及对nDNA引物各种修饰位置的试验和讨论。总之,与未修饰DNA相比,nDNA作为PCR和RT-PCR引物表现出卓越的性能,有望在需要增强特异性的各种应用中得到拓展。