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Unnatural Substrate Repertoire Of A, B, And X Family Dnarnpolymerases

机译:A,B和X家族Dnarnpolymerase的非自然底物库

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As part of an effort to develop unnatural base pairs that are stable and replicable in DNA, we examined the ability of five different polymerases to replicate DNA containing four different unnatural nucleotides bearing predominantly hydrophobic nucleobase analogs. The unnatural pairs were developed based on intensive studies using the Klenow fragment of DNA polymerase I from E. coli (Kf) and found to be recognized to varying degrees. The five additional polymerases characterized here include family A polymerases from bacteriophage T7 and Thermus aquaticus, family B polymerases from Thermococcus litoralis and Thermococcus 9°N-7, and the family X polymerase, human polymerase β. While we find that some aspects of unnatural base pair recognition are conserved among the polymerases, for example, the pair formed between two d3FB nucleotides is typically well recognized, the detailed recognition of most of the unnatural base pairs is generally polymerase dependent. In contrast, we find that the pair formed between d5SICS and dMMO2 is generally well recognized by all of the polymerases examined, suggesting that the determinants of efficient and general recognition are contained within the geometric and electronic structure of these unnatural nucleobases themselves. The data suggest that while the d3FB:d3FB pair is sufficiently well recognized by several of the polymerases for in vitro applications, the d5SICS:dMMO2 heteropair is likely uniquely promising for in vivo use. T7-mediated replication is especially noteworthy due to strong mispair discrimination.
机译:作为开发在DNA中稳定且可复制的非天然碱基对的努力的一部分,我们检查了五种不同的聚合酶复制包含四个主要带有疏水性核碱基类似物的非天然核苷酸的DNA的能力。非自然对是基于大量研究,使用来自大肠杆菌(Kf)的DNA聚合酶I的Klenow片段开发出来的,并发现了不同程度的识别。这里表征的另外五种聚合酶包括来自噬菌体T7和水生栖热菌(Thermus aquaticus)的A族聚合酶,来自滨海热球菌和9°N-7的热球菌的B族聚合酶,以及X族,人聚合酶β。尽管我们发现聚合酶之间保留了非天然碱基对识别的某些方面,例如,通常很好地识别了两个d3FB核苷酸之间形成的对,但大多数非天然碱基对的详细识别通常取决于聚合酶。相反,我们发现在d5SICS和dMMO2之间形成的对通常被所有检测的聚合酶很好地识别,这表明有效和普遍识别的决定因素包含在这些非天然核碱基本身的几何和电子结构中。数据表明,尽管d3FB:d3FB对已被几种聚合酶充分良好地识别以用于体外应用,但d5SICS:dMMO2杂对可能在体内使用方面具有独特的前景。由于强烈的配对错误歧视,T7介导的复制特别值得注意。

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