DNA聚合酶
聚合酶
化学
DNA
环介导等温扩增
核酸
核苷酸
多重位移放大
DNA钳
分子生物学
生物物理学
立体化学
生物化学
聚合酶链反应
生物
基因
逆转录酶
DNA提取
作者
Р.Р. Гарафутдинов,Aidar R. Gilvanov,O. Yu. Kupova,Assol R. Sakhabutdinova
标识
DOI:10.1016/j.ijbiomac.2020.08.028
摘要
Abstract Over the last two decades, the isothermal amplification has become actively used for nucleic acids analysis. To perform isothermal techniques, DNA polymerases with strand-displacement activity are needed, and Bst exo- polymerase is one of the most widely used. However, Bst exo- is prone to non-specific DNA synthesis (e.g., DNA multimerization) occurring in the absence of the DNA target of interest. Here, we report on the activity of Bst exo- in the presence of Mg2+, Mn2+, Ca2+, Cd2+, Co2+, Cu2+, Ni2+ and Zn2+ in the model molecular systems which included amplification of circular and linear DNA templates; conditions providing effective and highly specific isothermal amplification were determined. It was found that amplification can proceed not only with Mg2+ but with Mn2+, Ca2+, Cd2+ and Cu2+ depending on the type of Bst exo- polymerase and the buffer. Manganese ions turned out to be the most suitable alternative cofactor, which prevents multimerization in some buffers. Molecular docking simulations showed the highest stability for the quaternary ‘polymerase-DNA-triphosphate-cations’ complexes containing Mg2+ and Mn2+, and the moderate one for complexes with Ca2+, Cd2+ and Cu2+. The frequency of nucleotide misincorporation increased in the following row: Mg2+ ≈ Mn2+ ≤ Cd2+
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