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Label-free colorimetric aptasensor for sensitive detection of ochratoxin A utilizing hybridization chain reaction

机译:利用杂交链反应灵敏检测of曲霉毒素A的无标记比色适体传感器

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The combination of high selectivity of aptamer with the peroxidase-mimicking property of DNAzyme has presented considerable opportunities for designing colorimetric aptasensor for detection of ochratoxin A (OTA). The activities of both aptamer (as biorecognition element) and DNAzyme (as signal amplification element) are blocked via base pairing in the hairpin structure. Hybridization chain reaction (HCR) between two hairpin DNAswas employed to further improve the sensitivity of this method. The presence of OTA triggers the opening of the hairpin structure and the beginning of HCR, which results in the release of many DNAzyme, and generates enhanced colorimetric signals, which is correlated to the amounts of OTA with linear range between 0.01 to 0.32 nM, and the limit of detection is 0.01 nM under optimal conditions. OTA in yellow rice wine and wheat flour samples was also detected using this method. We demonstrate that a new colorimetric method for the detection of OTA has been established, which is simple, easy to conduct, label-free, sensitive, high throughput, and cost-saving. (C) 2014 Elsevier B.V. All rights reserved.
机译:适体的高选择性与DNAzyme的过氧化物酶模拟特性相结合,为设计用于检测曲霉毒素A(OTA)的比色适体传感器提供了巨大的机会。适体(作为生物识别元件)和DNAzyme(作为信号放大元件)的活性均通过发夹结构中的碱基配对被阻断。利用两个发夹DNA之间的杂交链反应(HCR)进一步提高了该方法的灵敏度。 OTA的存在触发发夹结构的开放和HCR的开始,这导致许多DNA酶的释放,并产生增强的比色信号,这与OTA的量相关,线性范围在0.01到0.32 nM之间,并且在最佳条件下,检测限为0.01 nM。黄酒和小麦粉样品中的OTA也使用这种方法进行了检测。我们证明,已经建立了一种检测OTA的新比色方法,该方法简单,易于执行,无标签,灵敏,高通量和节省成本。 (C)2014 Elsevier B.V.保留所有权利。

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