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

机译:通过将石墨烯与双相核酸酶组合的MiR-205测定的信号放大方法

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摘要

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-1 with a linear range of 5-40 nmol L-1. 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.
机译:由于微小RNA-205(MIR-205)是鼻咽癌(NPC)的抗辐射的预测生物标志物中,miR-205是一种用于开发个性化的策略NPC的治疗具有重要的定量检测。在该研究中,基于对荧光信号放大,为的miR-205的设计的高灵敏度检测方法中的氧化石墨烯传感器和双工特异性核酸酶(DSN)。当采用靶回收机构,其中,单个的miR-205靶触发许多DNA探针信号的裂解。该方法示出了分析的miR-205在溶液中的能力,并且可以在检测的浓度的miR-205低达132皮摩尔L-1用5-40纳摩尔L-1的线性范围内。此外,该方法是特异性的,因为它的靶miRNA和具有单碱基,双基和三个碱基错配,以及其它的miRNA的序列之间进行区分。考虑到简单性和出色的灵敏度/特异性,它是有前途的抗辐射研究以及NPC的早期临床诊断中的应用。

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    《RSC Advances》 |2019年第47期|共6页
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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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