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小分子偶联携带噻唑橙碱基替代物的肽核酸对流感 A 病毒 RNA 启动子柄部结构的荧光传感

Fluorescence Sensing of the Panhandle Structure of the Influenza A Virus RNA Promoter by Thiazole Orange Base Surrogate-Carrying Peptide Nucleic Acid Conjugated with Small Molecule.

机构信息

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

Department of Kampo and Integrative Medicine, Graduate School of Medicine, Tohoku University, Sendai 980-8575, Japan.

出版信息

Anal Chem. 2022 Jun 7;94(22):7814-7822. doi: 10.1021/acs.analchem.1c05488. Epub 2022 May 23.

Abstract

We have developed a new class of triplex-forming peptide nucleic acid (PNA)-based fluorogenic probes for sensing of the panhandle structure of the influenza A virus (IAV) RNA promoter region. Here, a small molecule (DPQ) capable of selectively binding to the internal loop structure was conjugated with triplex-forming forced intercalation of the thiazole orange (tFIT) probe with natural PNA nucleobases. The resulting conjugate, tFIT-DPQ, showed a significant light-up response (83-fold) upon strong ( = 107 nM) and structure-selective binding to the IAV RNA promoter region under physiological conditions (pH 7.0, 100 mM NaCl). We demonstrated the conjugation of these two units through the suitable spacer was key to show useful binding and fluorogenic signaling functions. tFIT-DPQ facilitated the sensitive and selective detection of IAV RNA based on its binding to the promoter region. Furthermore, we found that tFIT-DPQ could work as a sensitive indicator for screening of test compounds targeting the IAV RNA promoter region in the fluorescence indicator displacement assay.

摘要

我们开发了一类新的三联体形成肽核酸(PNA)荧光探针,用于检测甲型流感病毒(IAV)RNA 启动子区域的发夹结构。在这里,一种能够选择性结合内部环结构的小分子(DPQ)与噻唑橙(tFIT)探针与天然 PNA 碱基的三联体形成强制嵌入结合。所得的缀合物 tFIT-DPQ 在生理条件下(pH 7.0,100 mM NaCl)与 IAV RNA 启动子区域强(= 107 nM)和结构选择性结合时表现出显著的光响应(83 倍)。我们证明了这两个单元的连接是通过合适的间隔物来展示有用的结合和荧光信号功能的关键。tFIT-DPQ 基于与启动子区域的结合,促进了对 IAV RNA 的敏感和选择性检测。此外,我们发现 tFIT-DPQ 可以作为荧光指示剂置换测定中筛选针对 IAV RNA 启动子区域的测试化合物的敏感指示剂。

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