首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Three-way junction DNA based electrochemical biosensor for microRNAs detection with distinguishable locked nucleic acid recognition and redox cycling signal amplification
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Three-way junction DNA based electrochemical biosensor for microRNAs detection with distinguishable locked nucleic acid recognition and redox cycling signal amplification

机译:基于三路结DNA的微瘤检测电化学生物传感器,可区分锁定核酸识别和氧化还原循环信号放大

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摘要

Herein, we present one three-way junction (TWJ) DNA based electrochemical biosensor for sensitive microRNAs detection with locked nucleic acid (LNA) as capture probe and enzyme-free redox cycling signal amplification strategy. LNA owns higher binding affinity and thermal stability compared to normal DNA sequence. In the presence of target microRNA (miRNA-21), novel TWJ structure can be specially triggered with the assistant of methylene blue (MB)-tagged DNA signal probe, thus producing an enhanced electrochemical current. Furthermore, a chemical reductant, tris (2-carboxyethyl) phosphine (TCEP), is adopted to lead a relayed electron transport between solution TCEP and TWJ-linked MB tag and amplified whole signal intensity. Based on the selectivity from target-induced LNA/DNA TWJ structure and enzyme-free MB cycling amplification strategy, the designed electrochemical biosensor exhibits sensitive miRNA-21 detection, with a linear range from 100 aM to 100 pM and a low detection limit of 77 aM. In addition, it can successfully discriminate the differences between the miRNA family members, presenting a promising response to the direct determination of target miRNA-21 in real biological fluids. Our work provides an alternative LNA-based electrochemical biosensor way in the area of miRNA diagnostics and clinical analysis without complicated enzyme/nanomaterials-assisted signal amplification.
机译:在此,我们提出了一种基于三向连接(TWJ)DNA的电化学生物传感器,以锁定核酸(LNA)为捕获探针,采用无酶氧化还原循环信号放大策略,用于敏感的微小RNA检测。与正常DNA序列相比,LNA具有更高的结合亲和力和热稳定性。在靶microRNA(miRNA-21)存在下,在亚甲蓝(MB)标记的DNA信号探针的辅助下,新的TWJ结构可以被特别触发,从而产生增强的电化学电流。此外,采用化学还原剂三(2-羧乙基)膦(TCEP)在溶液TCEP和TWJ连接的MB标记之间进行电子传递,并放大整个信号强度。基于靶诱导LNA/DNA TWJ结构的选择性和无酶MB循环扩增策略,设计的电化学生物传感器具有灵敏的miRNA-21检测,线性范围为100μm至100μm,低检测限为77μm。此外,它还可以成功地区分miRNA家族成员之间的差异,对直接测定真实生物液体中的靶miRNA-21表现出良好的反应。我们的工作为miRNA诊断和临床分析领域提供了一种基于LNA的电化学生物传感器替代方法,无需复杂的酶/纳米材料辅助信号放大。

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