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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 >Design and development of PCR-free highly sensitive electrochemical assay for detection of telomerase activity using Nano-based (liposomal) signal amplification platform
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Design and development of PCR-free highly sensitive electrochemical assay for detection of telomerase activity using Nano-based (liposomal) signal amplification platform

机译:基于纳米(脂质体)信号放大平台的免PCR高灵敏度电化学检测端粒酶活性的设计与开发

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摘要

Telomerase, which has been detected in almost all kinds of cancer tissues, is considered as an important tumor marker for early cancer diagnostics. In the present study, an electrochemical method based on liposomal signal amplification platform is proposed for simple, PCR-free, and highly sensitive detection of human telomerase activity, extracted from A549 cells. In this strategy, telomerase reaction products, which immobilized on streptavidin-coated microplate, hybridized with biotinylated capture probes. Then, dopamine-loaded biotinylated liposomes are attached through streptavidin to biotinylated capture probes. Finally, liposomes are ruptured by methanol and the released-dopamine is subsequently measured using differential pulse voltammetry technique by multi-walled carbon nanotubes modified glassy carbon electrode. Using this strategy, the telomerase activity extracted from 10 cultured cancer cells could be detected. Therefore, this approach affords high sensitivity for telomerase activity detection and it can be regarded as an alternative to telomeric repeat amplification protocol assay, having the advantages of simplicity and less assay time. (C) 2016 Elsevier B.V. All rights reserved.
机译:端粒酶已在几乎所有类型的癌症组织中检测到,被认为是早期癌症诊断的重要肿瘤标志物。在本研究中,提出了一种基于脂质体信号放大平台的电化学方法,用于从A549细胞提取的人类端粒酶活性的简单,无PCR和高灵敏度检测。在这种策略中,固定在链霉亲和素包被的微板上的端粒酶反应产物与生物素化的捕获探针杂交。然后,将负载多巴胺的生物素化脂质体通过链霉亲和素连接到生物素化捕获探针上。最后,脂质体被甲醇破坏,随后使用差分脉冲伏安法通过多壁碳纳米管修饰的玻碳电极测量释放的多巴胺。使用这种策略,可以检测到从10个培养的癌细胞中提取的端粒酶活性。因此,该方法为端粒酶活性检测提供了高灵敏度,并且可以被认为是端粒重复扩增方案测定的替代方法,具有简单且测定时间短的优点。 (C)2016 Elsevier B.V.保留所有权利。

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