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Proximity Hybridization Regulated DNA Biogate for Sensitive Electrochemical Immunoassay

机译:邻近杂交调节DNA Biogate用于灵敏的电化学免疫测定

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摘要

An electrochemical DNA biogate was designed for highly sensitive homogeneous electrochemical immunoassay by combining target-induced proximity hybridization with a mesoporous silica nanoprobe (MSN). The electroactive methylene blue (MB) was sealed in the inner pores of MSN with single-stranded DNA. In the presence of target protein and two DNA-labeled antibodies, the formed proximate complex could hybridize with the DNA strand to form a rigid double-stranded structure and thus open the biogate, which led to the release of MB entrapped in the MSN. The target protein-dependent amount of released MB could be conveniently monitored with a screen-printed carbon electrode. Moreover, the detachment process of MB could be further amplified with an in situ enzymatic recycling binding of the proximate complex with the single-stranded DNA. Using prostate-specific antigen as a model target, the proposed assay showed a wide detection range from 0.002 to 100 ng mL~(-1) with a detection limit of 1.3 pg mL~(-1). This strategy was simple and universal for various analytes with different affinity ligands. This method possessed great potential for convenient point-of-care testing and commercial application.
机译:通过将靶标诱导的邻近杂交与中孔二氧化硅纳米探针(MSN)结合,将电化学DNA生物门设计用于高灵敏度的均相电化学免疫分析。用单链DNA将电活性亚甲基蓝(MB)密封在MSN的内孔中。在存在靶蛋白和两种DNA标记的抗体的情况下,形成的邻近复合物可与DNA链杂交形成刚性的双链结构,从而打开生物门,从而释放了MSN中包裹的MB。可以通过丝网印刷的碳电极方便地监测目标蛋白依赖的MB释放量。此外,MB的分离过程可以通过将近邻复合物与单链DNA进行原位酶循环结合而进一步放大。以前列腺特异性抗原为模型靶标,所提出的检测方法检测范围为0.002〜100 ng mL〜(-1),检测限为1.3 pg mL〜(-1)。对于具有不同亲和力配体的各种分析物,此策略既简单又通用。该方法具有便利的即时检验和商业应用的巨大潜力。

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