Koukhareva Inna, Haoqiang Huang, Yee Joyclyn, Shum Jonathan, Paul Natasha, Hogrefe Richard I, Lebedev Alexandre V
Trilink BioTechnologies, Inc., 9955 Mesa Rim Road, San Diego, CA 92121, USA.
Nucleic Acids Symp Ser (Oxf). 2008(52):259-60. doi: 10.1093/nass/nrn131.
Several 3'-ether and 3'-ester derivatives of 2'-deoxyribonucleoside 5'-triphosphates (dNTPs) were prepared. These dNTP derivatives were not substrates for DNA polymerase and did not support primer extension at room temperature. However, by short pre-heating to 95 degrees C in PCR buffer, these 3'-modified dNTPs can be converted to corresponding unmodified natural dNTPs that efficiently support PCR amplification. The analysis of PCR products obtained with 3'-modified dNTPs revealed a significant improvement in PCR performance resulting in higher amplicon yield and reduced formation of off-target products (mis-priming and primer dimer). Among the studied 3'-modified dNTPs, the 3'-tetrahydrofuranyl derivatives showed the best results.
制备了几种2'-脱氧核糖核苷5'-三磷酸(dNTP)的3'-醚和3'-酯衍生物。这些dNTP衍生物不是DNA聚合酶的底物,在室温下不支持引物延伸。然而,通过在PCR缓冲液中短时间预热至95℃,这些3'-修饰的dNTP可以转化为相应的未修饰天然dNTP,从而有效地支持PCR扩增。对用3'-修饰的dNTP获得的PCR产物的分析表明,PCR性能有显著改善,导致更高的扩增子产量和减少非靶标产物(错配引物和引物二聚体)的形成。在所研究的3'-修饰的dNTP中,3'-四氢呋喃基衍生物显示出最佳结果。