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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Nanocatalyst-based assay using DNA-conjugated Au nanoparticles for electrochemical DNA detection
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Nanocatalyst-based assay using DNA-conjugated Au nanoparticles for electrochemical DNA detection

机译:基于DNA的金纳米颗粒用于电化学DNA检测的基于纳米催化剂的测定

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摘要

Compared to enzymes, Au nanocatalysts show better long-term stability and are more easily prepared. Au nanoparticles (AuNPs) are used as catalytic labels to achieve ultrasensitive DNA detection via fast catalytic reactions. In addition, magnetic beads (MBs) are employed to permit low nonspecific binding of DNA-conjugated AuNPs and to minimize the electrocatalytic Current of AuNPs as well as to take advantage of easy magnetic separation. In a sandwich-type elcetrochemical sensor, capture-probe-conjugated MBs and an indium-tin oxide electrode modified with a partially ferrocene-modified dendrimer act as the target-binding surface and the signal-generating surface, respectively. A thiolated detection-probe-conjugated AuNP exhibits a high level Of unblocked active sites and permits the easy access of p-nitrophenol and NaBH4 to these sites. Electroactive p-aminophenol is generated at these sites and is then electrooxidized to p-quinoneimine at the electrode. The p-aminophenol redox cycling by NaBH4 offers large signal amplification. The nonspecific binding of detection-probe-conjugated AuNPs is lowered by washing DNA-linked MB-AuNP assemblies with a formamide-containing solution, and the electrocatalytic oxidation of NaBH4 by AuNPs is minimized because long-range electron transfer between the electrode and the AuNPs bound to MBs is not feasible. The high signal amplification and low background Current enable the detection of 1 fM target DNA.
机译:与酶相比,金纳米催化剂显示出更好的长期稳定性并且更容易制备。金纳米颗粒(AuNPs)用作催化标记,可通过快速催化反应实现超灵敏的DNA检测。此外,采用磁珠(MBs)允许与DNA偶联的AuNPs的低非特异性结合,并使AuNPs的电催化电流最小化,并利用容易的磁分离优势。在夹心型电化学传感器中,与捕获探针结合的MBs和经部分二茂铁改性的树枝状大分子修饰的铟锡氧化物电极分别充当目标结合表面和信号产生表面。硫醇化的检测探针结合的AuNP表现出高水平的未封闭活性位点,并允许对硝基苯酚和NaBH4轻松进入这些位点。在这些位点产生电活性对氨基苯酚,然后在电极上被电氧化为对苯二甲亚胺。 NaBH4的对氨基苯酚氧化还原循环可提供大信号放大。通过用含甲酰胺的溶液洗涤DNA链接的MB-AuNP组件,可以降低与检测探针偶联的AuNP的非特异性结合,并且由于电极和AuNP之间的长距离电子转移,使AuNP对NaBH4的电催化氧化作用降至最低。绑定到MB是不可行的。高信号放大和低背景电流使得能够检测1 fM靶DNA。

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