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天然RNA的位点选择性修饰与标记

Site-Selective Modification and Labeling of Native RNA.

作者信息

Kha Tuan-Khoa, Zhao Yiran, Zhu Ru-Yi

机构信息

Department of Chemistry, National University of Singapore, Singapore, 117544.

出版信息

Chemistry. 2025 Feb 25;31(12):e202404244. doi: 10.1002/chem.202404244. Epub 2025 Feb 9.

Abstract

Ribonucleic acid (RNA) plays a pivotal role in regulating biological processes within living systems, with modified nucleosides serving as critical modulators of various aspects of biological functions. Therefore, the development of efficient methodologies for late-stage, site-selective RNA modification is of considerable interest, as it facilitates the functional exploration of RNA chemical modifications and their implications for therapeutic applications. Precise RNA modification holds significant promise for the treatment of genetic diseases by enabling the correction of mutated nucleobases to their wild-type forms. Additionally, the site-selective incorporation of synthetic labeling groups into RNA provides invaluable tools for structural and functional studies, thereby uncovering previously hidden dimensions of RNA's role in biological systems. In this review, we provide a comprehensive overview of three principal approaches to site-selective, late-stage RNA modifications: enzyme-mediated strategies, catalytic nucleic acid-based techniques, and chemical methodologies. These approaches predominantly target the nucleobase or the 2'-hydroxyl (2'-OH) group of RNA nucleosides. We evaluate the advantages and limitations of each strategy and discuss future directions for advancing this field of research.

摘要

核糖核酸(RNA)在调节生物系统中的生物过程中起着关键作用,修饰核苷作为生物功能各个方面的关键调节因子。因此,开发用于后期、位点选择性RNA修饰的有效方法备受关注,因为它有助于对RNA化学修饰进行功能探索及其在治疗应用中的意义。精确的RNA修饰通过将突变的核苷酸碱基校正为野生型形式,在治疗遗传疾病方面具有巨大潜力。此外,将合成标记基团位点选择性地掺入RNA为结构和功能研究提供了宝贵工具,从而揭示了RNA在生物系统中作用的先前隐藏的层面。在本综述中,我们全面概述了位点选择性、后期RNA修饰的三种主要方法:酶介导策略、基于催化核酸的技术和化学方法。这些方法主要针对RNA核苷的核苷酸碱基或2'-羟基(2'-OH)基团。我们评估了每种策略的优缺点,并讨论了推进该研究领域的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba5a/11855268/79d39558c3f2/CHEM-31-e202404244-g010.jpg

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