首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >An ultrasensitive electrochemical biosensor for detection of microRNA-21 based on redox reaction of ascorbic acid/iodine and duplex-specific nuclease assisted target recycling
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An ultrasensitive electrochemical biosensor for detection of microRNA-21 based on redox reaction of ascorbic acid/iodine and duplex-specific nuclease assisted target recycling

机译:超致敏电化学生物传感器,用于检测抗坏血酸/碘和双链特异性核酸酶辅助靶回收的氧化还原反应

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摘要

A novel electrochemical biosensor was developed based on multiwall carbon nanotubes/graphene oxide nanoribbons (MWCNTs/GONRs) for sensitive analysis of microRNA-21. Signal-amplified strategy was achieved by duplex-specific nuclease assisted target recycling and alkaline phosphatase-induced redox reactions. At the fabrication process of the sensor, ssDNA capture probes were immobilized on the surface of the MWCNTs@GONRs/AuNPs modified electrode through the Au-S bond, and the streptavidin-conjugated alkaline phosphatase (SA-ALP) was attached to the end of the probe. In the absence of miRNA-21, SA-ALP catalysed the conversion of ascorbic acid 2-phosphate (AAP) into ascorbic acid (AA), triggered a redox reaction under iodine, producing a marked electrochemical response. When miRNA-21 was hybridized to the capture probe, the duplex would be cleaved by the duplex-specific nuclease (DSN), causing the electrochemical signals being significantly decreased as a result of SA-ALP detached from the electrode surface. Under the optimized conditions, our biosensor showed satisfactory sensitivity (detection limit, 0.034 fM), excellent selectivity and good accuracy (recoveries, 77.4-120.2%; RSD, 5.2-7.3%) after systematic evaluations. The proposed approach was applied to detect miRNA-21 from human serum samples, which indicated that it was reliable and could be widely used as an effective tool for rapid detection of the target in serums.
机译:基于多壁碳纳米管/石墨烯氧化物纳米纤维(MWCNTS / GONRS)开发了一种新型电化学生物传感器,用于微RNA-21的敏感性分析。通过双相特异性核酸酶辅助靶再循环和碱性磷酸酶诱导的氧化还原反应实现了信号扩增策略。在传感器的制造过程中,通过AU-S键将SSDNA捕获探针固定在MWCNTS / AUNPS改性电极的表面上,并且链霉抗生物素蛋白 - 缀合的碱性磷酸酶(SA-ALP)连接到末端探针。在没有miRNA-21的情况下,SA-ALP将抗坏血酸2-磷酸(AAP)的转化为抗坏血酸(AA),引发碘下的氧化还原反应,产生标记的电化学反应。当MiRNA-21与捕获探针杂交时,双工将通过双相特异性核酸酶(DSN)切割,导致电化学信号由于从电极表面分离而导致的电化学信号显着降低。在优化的条件下,我们的生物传感器显示出令人满意的灵敏度(检测限,0.034 Fm),优异的选择性和良好的准确度(回收率,77.4-120.2%; RSD,5.2-7.3%)。拟议的方法被应用于从人血清样品中检测miRNA-21,这表明它是可靠的并且可以广泛用作快速检测血清靶标的有效工具。

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