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Cascade Signal Amplification Based on Copper Nanoparticle-Reported Rolling Circle Amplification for Ultrasensitive Electrochemical Detection of the Prostate Cancer Biomarker

机译:基于铜纳米颗粒报道的滚动圆放大的级联信号放大,用于前列腺癌生物标志物的超灵敏电化学检测

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An ultrasensitive and highly selective electrochemical assay was first attempted by combining the rolling circle amplification (RCA) reaction with poly(thymine)-templated copper nanoparticles (CuNPs) for cascade signal amplification. As proof of concept, prostate specific antigen (PSA) was selected as a model target. Using a gold nanoparticle (AuNP) as a carrier, we synthesized the primerAuNPaptamer bioconjugate for signal amplification by increasing the primer/aptamer ratio. The specific construction of primerAuNPaptamer/PSA/anti-PSA sandwich structure triggered the effective RCA reaction, in which thousands of tandem poly(thymine) repeats were generated and directly served as the specific templates for the subsequent CuNP formation. The signal readout was easily achieved by dissolving the RCA product-templated CuNPs and detecting the released copper ions with differential pulse stripping voltammetry. Because of the designed cascade signal amplification strategy, the newly developed method achieved a linear range of 0.05-500 fg/mL, with a remarkable detection limit of 0.020 +/- 0.001 fg/mL PSA. Finally, the feasibility of the developed method for practical application was investigated by analyzing PSA in the real clinical human serum samples. The ultrasensitivity, specificity, convenience, and capability for analyzing the clinical samples demonstrate that this method has great potential for practical disease diagnosis applications.
机译:首先尝试通过将滚环扩增(RCA)反应与以聚胸腺嘧啶为模板的铜纳米颗粒(CuNPs)结合以进行级联信号放大来进行超灵敏和高度选择性的电化学测定。作为概念证明,选择前列腺特异性抗原(PSA)作为模型靶标。我们使用金纳米粒子(AuNP)作为载体,通过增加引物/适体比率合成了用于信号放大的引物AuNPaptamer生物缀合物。引物AuNPaptamer / PSA /抗PSA三明治结构的特殊构建触发了有效的RCA反应,其中产生了数千个串联的聚胸腺嘧啶重复序列,并直接用作后续CuNP形成的特异性模板。通过溶解RCA产物模板化的CuNPs并使用差分脉冲溶出伏安法检测释放的铜离子,可以轻松实现信号读取。由于设计了级联信号放大策略,新开发的方法实现了0.05-500 fg / mL的线性范围,且PSA的检测限很低,为0.020 +/- 0.001 fg / mL。最后,通过分析真实临床人血清样本中的PSA,研究了所开发方法在实际中的可行性。超灵敏性,特异性,方便性和对临床样品进行分析的能力证明,该方法在实际疾病诊断应用中具有巨大潜力。

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