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基于二茂铁与钌(bpy)功能化金属有机框架之间的淬灭效应的信号关闭电致化学发光生物传感平台用于检测甲基化 RNA。

Signal-Off Electrogenerated Chemiluminescence Biosensing Platform Based on the Quenching Effect between Ferrocene and Ru(bpy)-Functionalized Metal-Organic Frameworks for the Detection of Methylated RNA.

机构信息

Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry and Materials Science , Northwest University , Xi'an 710069 , P. R. China.

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems , Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190 , P. R. China.

出版信息

Anal Chem. 2019 Sep 17;91(18):11840-11847. doi: 10.1021/acs.analchem.9b02569. Epub 2019 Sep 5.

Abstract

N-methyladenine (mA), one of the most common chemical modifications of eukaryotic RNA, participates in many important biological processes. An effective strategy for the quantitative determination of mA is of great significance. Herein, we used methylated microRNA-21 (miRNA21) as the model target to propose a simple and sensitive electrogenerated chemiluminescence (ECL) biosensing platform to detect a specific mA RNA sequence. This strategy is based on the fact that the anti-mA-antibody can specifically recognize and bind to the mA site in the RNA sequence, resulting in a quenching effect between Ru(bpy)-functionalized metal-organic frameworks and ferrocene. Luminescent metal-organic frameworks (Ru@MOFs) not only act as ECL indicators but also serve as nanoreactors for the relative ECL reactions owing to their porous or multichannel structure, which overcomes the fact that Ru(bpy) is easily released when used for aqueous-phase detection, thus enhancing the ECL efficiency. Moreover, the ECL method has fewer modification steps and uses only one antibody to recognize the target RNA sequence, which simplifies the operation process and reduces the detection time, presenting a wide linear range (0.001-10 nM) for mA RNA determination with a low detection limit (0.0003 nM). Additionally, this developed strategy was validated for mA RNA detection in human serum. Thus, the ECL biosensing method provides a new method for mA RNA determination that is simple, highly specific, and sensitive.

摘要

N6-甲基腺嘌呤(mA)是真核 RNA 中最常见的化学修饰之一,参与许多重要的生物学过程。因此,建立一种有效的 mA 定量测定方法具有重要意义。本文以甲基化 microRNA-21(miRNA21)为模型靶标,提出了一种简单、灵敏的电致化学发光(ECL)生物传感平台,用于检测特定的 mA RNA 序列。该策略基于这样一个事实,即抗-mA 抗体可以特异性识别和结合 RNA 序列中的 mA 位点,从而导致 Ru(bpy)功能化金属有机骨架和二茂铁之间的猝灭效应。发光金属-有机骨架(Ru@MOFs)不仅由于其多孔或多通道结构而作为 ECL 指示剂,而且还作为相对 ECL 反应的纳米反应器,克服了 Ru(bpy)在用于水相检测时容易释放的事实,从而提高了 ECL 效率。此外,ECL 方法的修饰步骤更少,并且仅使用一种抗体来识别靶 RNA 序列,从而简化了操作过程并减少了检测时间,为 mA RNA 测定提供了较宽的线性范围(0.001-10 nM)和较低的检测限(0.0003 nM)。此外,该开发的策略已被验证用于人血清中 mA RNA 的检测。因此,ECL 生物传感方法为 mA RNA 的测定提供了一种简单、高度特异性和灵敏的新方法。

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