Center for iPS Cell Research and Application, Kyoto University, 53 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.
Graduate School of Medicine, Kyoto University, Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Nucleic Acids Res. 2023 Apr 11;51(6):e34. doi: 10.1093/nar/gkad019.
The potential of synthetic mRNA as a genetic carrier has increased its application in scientific fields. Because the 5' cap regulates the stability and translational activity of mRNAs, there are concerted efforts to search for and synthesize chemically-modified 5' caps that improve the functionality of mRNA. Here, we report an easy and efficient method to synthesize functional mRNAs by modifying multiple 5' cap analogs using a vaccinia virus-capping enzyme. We show that this enzyme can introduce a variety of GTP analogs to the 5' end of RNA to generate 5' cap-modified mRNAs that exhibit different translation levels. Notably, some of these modified mRNAs improve translation efficiency and can be conjugated to chemical structures, further increasing their functionality. Our versatile method to generate 5' cap-modified mRNAs will provide useful tools for RNA therapeutics and biological research.
作为一种遗传载体,合成 mRNA 的潜力增加了其在科学领域的应用。由于 5' 帽结构调节着 mRNA 的稳定性和翻译活性,因此人们正在积极努力寻找和合成化学修饰的 5' 帽结构,以提高 mRNA 的功能。在这里,我们报告了一种使用牛痘病毒加帽酶修饰多种 5' 帽类似物来合成功能性 mRNA 的简单而高效的方法。我们表明,该酶可以将各种 GTP 类似物引入 RNA 的 5' 端,生成具有不同翻译水平的 5' 帽修饰的 mRNA。值得注意的是,其中一些修饰的 mRNA 提高了翻译效率,并可以与化学结构连接,进一步提高了它们的功能。我们生成 5' 帽修饰 mRNA 的多功能方法将为 RNA 治疗学和生物学研究提供有用的工具。