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用于双链RNA结构强制嵌入传感的基于三链形成肽核酸的荧光探针设计。

Design of triplex-forming peptide nucleic acid-based fluorescent probes for forced intercalation sensing of double-stranded RNA structures.

作者信息

Sato Yusuke, Sato Takaya, Lee En Ting Tabitha, Chiba Toshiki, Tanabe Takaaki, Yoshino Yukina, Nishizawa Seiichi

机构信息

Department of Chemistry, Graduate School of Science, Tohoku University, Aoba-Ku, Sendai, 980-8578, Japan.

出版信息

Anal Sci. 2025 May;41(5):531-539. doi: 10.1007/s44211-024-00713-5. Epub 2025 Jan 17.

Abstract

The diverse functional roles of RNA within cells have led to a growing interest in developing RNA-binding fluorescent probes to investigate RNA functions. In particular, the probes for double-stranded RNA (dsRNA) structures are of significant value given the importance of the secondary and tertiary RNA structures on their biologic functions. This review highlights our recent efforts on the development of triplex-forming peptide nucleic acid (TFP)-based probes for fluorescence sensing of dsRNA structures. We demonstrated that the forced intercalation of asymmetric cyanine dyes integrated as base surrogate within the probes was useful for achieving significant light-up response toward target dsRNAs. We also showed that the TFP probes conjugated with small RNA-binding molecules facilitated the fluorescence sensing of biologic relevant dsRNAs containing unpaired nucleobases. The binding and fluorescence signaling functions of such probes were discussed, emphasizing their potential as analytical tools for studying dsRNA structures.

摘要

RNA在细胞内具有多种功能作用,这使得人们对开发用于研究RNA功能的RNA结合荧光探针的兴趣日益浓厚。特别是,鉴于RNA二级和三级结构对其生物学功能的重要性,双链RNA(dsRNA)结构的探针具有重要价值。本综述重点介绍了我们最近在开发基于三链形成肽核酸(TFP)的探针用于dsRNA结构荧光传感方面所做的努力。我们证明,将不对称花青染料作为碱基替代物强制插入探针中,有助于实现对目标dsRNA的显著点亮响应。我们还表明,与小RNA结合分子偶联的TFP探针促进了对含有未配对核碱基的生物学相关dsRNA的荧光传感。讨论了此类探针的结合和荧光信号功能,强调了它们作为研究dsRNA结构的分析工具的潜力。

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