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通过将氧化石墨烯与双链特异性核酸酶相结合的miR-205检测信号放大方法。

Signal amplification method for miR-205 assay through combining graphene oxide with duplex-specific nuclease.

作者信息

Yang Zhaoqi, Qin Lan, Yang Dutao, Chen Weixia, Qian Yue, Jin Jian

机构信息

School of Pharmaceutical Sciences, Jiangnan University Wuxi 214122 China

出版信息

RSC Adv. 2019 Aug 30;9(47):27341-27346. doi: 10.1039/c9ra04663a. eCollection 2019 Aug 29.

Abstract

Since microRNA-205 (miR-205) is a predictive biomarker for anti-radiation of nasopharyngeal carcinoma (NPC), quantitative detection of miR-205 is important for developing personalized strategies for the treatment of NPC. In this investigation, based on the graphene oxide sensor and duplex specific nuclease (DSN) for fluorescence signal amplification, a highly sensitive detection method for miR-205 was designed. A target-recycling mechanism is employed, where a single miR-205 target triggers the cleavage of many DNA signal probes. The method shows the ability to analyze miR-205 in solution, and it can detect miR-205 at concentrations as low as 132 pmol L with a linear range of 5-40 nmol L. Furthermore, the method is specific in that it distinguishes between a target miRNA and a sequence with single base, double base and three base mismatches, as well as other miRNAs. Considering simplicity and excellent sensitivity/specificity, it is promising for applications in radioresistance studies as well as the early clinical diagnosis of NPC.

摘要

由于微小RNA-205(miR-205)是鼻咽癌(NPC)抗辐射的预测生物标志物,因此miR-205的定量检测对于制定NPC个性化治疗策略至关重要。在本研究中,基于氧化石墨烯传感器和用于荧光信号放大的双链特异性核酸酶(DSN),设计了一种高灵敏度的miR-205检测方法。采用了靶循环机制,其中单个miR-205靶标触发许多DNA信号探针的切割。该方法能够分析溶液中的miR-205,其线性范围为5-40 nmol/L,能够检测低至132 pmol/L浓度的miR-205。此外,该方法具有特异性,能够区分靶标微小RNA与具有单碱基、双碱基和三碱基错配的序列以及其他微小RNA。考虑到其简便性和出色的灵敏度/特异性,该方法在放射抗性研究以及NPC的早期临床诊断中具有应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c1d/9070658/1a38076761a6/c9ra04663a-s1.jpg

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