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DNA-Redox Cation Interaction Improves the Sensitivity of an Electrochemical Immunosensor for Protein Detection

机译:DNA-氧化还原阳离子相互作用提高了用于蛋白质检测的电化学免疫传感器的灵敏度

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摘要

A simple DNA-redox cation interaction enhancement strategy has been developed to improve the sensitivity of electrochemical immunosensors for protein detection. Instead of labeling with fluorophores or redox-active groups, the detection antibodies were tethered with DNA single strands. Based on the electrostatic interaction between redox cations ([Ru(NH3)6]3+) and negatively charged DNA backbone, enhanced electrochemical signals were obtained. Human chorionic gonadotropin (hCG) detection has been performed as a trial analysis. A linear response range up to the concentration of 25 mIU/mL and a detection limit of 1.25 mIU/mL have been achieved, both are comparable with the ultrasensitive enzyme-linked immunosorbent assay (ELISA) tests. The method also shows great selectivity towards hCG over other hormones such as thyroid stimulating hormone (TSH) and follicle stimulating hormone (FSH). By and large, our approach bears the merits of cost effectiveness and simplicity of instrumentation in comparison with conventional optical detection methods.
机译:已经开发了一种简单的DNA-氧化还原阳离子相互作用增强策略,以提高用于蛋白质检测的电化学免疫传感器的灵敏度。代替用荧光团或氧化还原活性基团标记,将检测抗体与DNA单链束缚在一起。基于氧化还原阳离子([Ru(NH3)6] 3 + )与带负电荷的DNA主链之间的静电相互作用,获得了增强的电化学信号。人绒毛膜促性腺激素(hCG)检测已作为试验分析进行。线性响应范围高达25 mIU / mL的浓度和1.25 mIU / mL的检出限,均与超灵敏酶联免疫吸附测定(ELISA)测试相当。该方法还显示出对hCG的选择性高于其他激素,例如甲状腺刺激激素(TSH)和卵泡刺激激素(FSH)。总的来说,与传统的光学检测方法相比,我们的方法具有成本效益和仪器简单的优点。

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