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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 >Paper-based electrochemiluminescence origami device for protein detection using assembled cascade DNA-carbon dots nanotags based on rolling circle amplification
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Paper-based electrochemiluminescence origami device for protein detection using assembled cascade DNA-carbon dots nanotags based on rolling circle amplification

机译:纸基电化学发光折纸装置,用于基于滚动环扩增的组装级联DNA-碳点纳米标签进行蛋白质检测

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摘要

In this work, we developed a cascade signal amplification strategy for detection of IgG antigen by combining the rolling circle amplification (RCA) technique with oligonucleotide functionalized carbon dots (CDs), based on a paper-based electrochemiluminescence (ECL) origami device (PECLOD) for the first time. In this PECLOD, three-dimensional (3D) macroporous Au-paper electrode was fabricated and employed as the working electrode for specific and efficient antibodies capture. The RCA product containing tandem-repeat sequences could serve as an excellent template for periodic assembly of CDs, which presented per protein recognition event to numerous CDs tags for ECL readout. Under the optimal conditions, the proposed strategy showed remarkable amplification efficiency, very little nonspecific adsorption with good stability, reproducibility, and accuracy. Using human IgG (H-IgG) as a model protein, the designed strategy was successfully demonstrated for the ultrasensitive detection of protein target. The results revealed that the strategy exhibited a dynamic response to H-IgG range from 1.0 fM to 25 pM with a limit of detection as low as 0.15 fM. Importantly, the methodology can be further extended to the detection of other proteins or biomarkers. (C) 2015 Elsevier B.V. All rights reserved.
机译:在这项工作中,我们基于纸基电化学发光(ECL)折纸设备(PECLOD),通过结合滚环扩增(RCA)技术和寡核苷酸官能化碳点(CD),开发了用于检测IgG抗原的级联信号放大策略。首次。在该PECLOD中,制造了三维(3D)大孔Au纸电极,并用作捕获特异性和有效抗体的工作电极。包含串联重复序列的RCA产品可以用作CD定期装配的出色模板,该CD可以将每个蛋白质识别事件提供给众多CD标签以进行ECL读出。在最佳条件下,所提出的策略显示出显着的扩增效率,极少的非特异性吸附,具有良好的稳定性,可重复性和准确性。使用人IgG(H-IgG)作为模型蛋白,成功地证明了设计的策略可用于蛋白靶标的超灵敏检测。结果表明,该策略对H-IgG的动态反应范围为1.0 fM至25 pM,检出限低至0.15 fM。重要的是,该方法可以进一步扩展到其他蛋白质或生物标记物的检测。 (C)2015 Elsevier B.V.保留所有权利。

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