Christensen Trevor A, Lee Kristi Y, Gottlieb Simone Z P, Carrier Mikayla B, Leconte Aaron M
W. M. Keck Science Department of Claremont McKenna, Pitzer, and Scripps Colleges Claremont CA USA
RSC Chem Biol. 2022 Jun 17;3(8):1044-1051. doi: 10.1039/d2cb00064d. eCollection 2022 Aug 3.
Nonnatural nucleic acids (xeno nucleic acids, XNA) can possess several useful properties such as expanded reactivity and nuclease resistance, which can enhance the utility of DNA as a biotechnological tool. Native DNA polymerases are unable to synthesize XNA, so, in recent years mutant XNA polymerases have been engineered with sufficient activity for use in processes such as PCR. While substantial improvements have been made, accuracy still needs to be increased by orders of magnitude to approach natural error rates and make XNA polymerases useful for applications that require high fidelity. Here, we systematically evaluate leading Taq DNA polymerase mutants for their fidelity during synthesis of 2'F XNA. To further improve their accuracy, we add mutations that have been shown to increase the fidelity of wild-type Taq polymerases, to some of the best current XNA polymerases (SFM4-3, SFM4-6, and SFP1). The resulting polymerases show significant improvements in synthesis accuracy. In addition to generating more accurate XNA polymerases, this study also informs future polymerase engineering efforts by demonstrating that mutations that improve the accuracy of DNA synthesis may also have utility in improving the accuracy of XNA synthesis.
非天然核酸(异种核酸,XNA)可具有多种有用特性,如反应活性增强和抗核酸酶能力,这可提高DNA作为生物技术工具的效用。天然DNA聚合酶无法合成XNA,因此近年来已设计出具有足够活性的突变型XNA聚合酶,可用于PCR等过程。虽然已取得显著进展,但准确性仍需提高几个数量级,以接近天然错误率,并使XNA聚合酶可用于需要高保真度的应用。在此,我们系统评估了主要的Taq DNA聚合酶突变体在合成2'F XNA过程中的保真度。为进一步提高其准确性,我们将已证明可提高野生型Taq聚合酶保真度的突变引入一些当前最佳的XNA聚合酶(SFM4-3、SFM4-6和SFP1)。所得聚合酶在合成准确性方面有显著提高。除了生成更准确的XNA聚合酶外,本研究还通过证明提高DNA合成准确性的突变也可能有助于提高XNA合成的准确性,为未来的聚合酶工程工作提供了参考。