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多胺通过修饰的嗜热聚合酶突变体促进异源核酸合成。

Polyamines promote xenobiotic nucleic acid synthesis by modified thermophilic polymerase mutants.

作者信息

Hoshino Hidekazu, Kasahara Yuuya, Obika Satoshi

机构信息

National Institutes of Biomedical Innovation, Health and Nutrition (NIBIOHN) 7-6-8 Saito-Asagi Ibaraki 567-0085 Osaka Japan

Graduate School of Pharmaceutical Sciences, Osaka University 1-6 Yamadaoka Suita 565-0871 Osaka Japan

出版信息

RSC Chem Biol. 2024 Apr 4;5(5):467-472. doi: 10.1039/d4cb00017j. eCollection 2024 May 8.

Abstract

The enzymatic synthesis of xenobiotic nucleic acids (XNA), which are artificially sugar-modified nucleic acids, is essential for the preparation of XNA libraries. XNA libraries are used in the selection of XNA aptamers and enzymes (XNAzymes). Efficient enzymatic synthesis of various XNAs can enable the screening of high-quality XNA aptamers and XNAzymes by expanding the diversity of XNA libraries and adding a variety of properties to XNA aptamers and XNAzymes. However, XNAs that form unstable duplexes with DNA, such as arabino nucleic acid (ANA), may dissociate during enzyme synthesis at temperatures suitable for thermophilic polymerases. Thus, such XNAs are not efficiently synthesised by the thermophilic polymerase mutants at the end of the sequence. This undesirable bias reduces the possibility of generating high-quality XNA aptamers and XNAzymes. Here, we demonstrate that polyamine-induced DNA/ANA duplex stabilisation promotes ANA synthesis that is catalysed by thermophilic polymerase mutants. Several polyamines, including spermine, spermidine, cadaverine, and putrescine promote ANA synthesis. The negative effect of polyamines on the fidelity of ANA synthesis was negligible. We also showed that polyamines promote the synthesis of other XNAs, including 2'-amino-RNA/2'-fluoro-RNA mixture and 2'--methyl-RNA. In addition, we found that polyamine promotes DNA synthesis from the 2'--methyl-RNA template. Polyamines, with the use of thermophilic polymerase mutants, may allow further development of XNA aptamers and XNAzymes by promoting the transcription and reverse transcription of XNAs.

摘要

异源核酸(XNA)是人工糖修饰的核酸,其酶促合成对于制备XNA文库至关重要。XNA文库用于筛选XNA适配体和酶(XNA酶)。通过扩大XNA文库的多样性并为XNA适配体和XNA酶添加各种特性,高效酶促合成各种XNA能够筛选高质量的XNA适配体和XNA酶。然而,与DNA形成不稳定双链体的XNA,如阿拉伯糖核酸(ANA),在适合嗜热聚合酶的温度下进行酶合成时可能会解离。因此,此类XNA在序列末端不能被嗜热聚合酶突变体高效合成。这种不良偏差降低了产生高质量XNA适配体和XNA酶的可能性。在此,我们证明多胺诱导的DNA/ANA双链体稳定促进了嗜热聚合酶突变体催化的ANA合成。包括精胺、亚精胺、尸胺和腐胺在内的几种多胺促进ANA合成。多胺对ANA合成保真度的负面影响可忽略不计。我们还表明,多胺促进其他XNA的合成,包括2'-氨基-RNA/2'-氟-RNA混合物和2'-甲基-RNA。此外,我们发现多胺促进从2'-甲基-RNA模板进行DNA合成。通过使用嗜热聚合酶突变体,多胺可能通过促进XNA的转录和逆转录来推动XNA适配体和XNA酶的进一步发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b61c/11078213/4ef87f139417/d4cb00017j-f1.jpg

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