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 >Electrochemical aptasensor based on the dual-amplification of G-quadruplex horseradish peroxidase-mimicking DNAzyme and blocking reagent-horseradish peroxidase
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Electrochemical aptasensor based on the dual-amplification of G-quadruplex horseradish peroxidase-mimicking DNAzyme and blocking reagent-horseradish peroxidase

机译:基于G-四倍体辣根过氧化物酶模拟DNAzyme和封闭剂-辣根过氧化物酶双重扩增的电化学适体传感器

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摘要

A simple electrochemical aptasensor for sensitive detection of thrombin was fabricated with G-quadruplex horseradish peroxidase-mimicking DNAzyme (hemin/G-quadruplex system) and blocking reagent-horseradish peroxidase as dual signal-amplification scheme. Gold nanoparticles (nano-Au) were firstly electrodeposited onto single wall nanotube (SWNT)-graphene modified electrode surface for the immobilization of electrochemical probe of nickel hexacyanoferrates nanoparticles (NiHCFNPs). Subsequently, another nano-Au layer was electrodeposited for further immobilization of thrombin aptamer (TBA), which later formed hemin/G-quadruplex system with hemin. Horseradish peroxidases (HRP) then served as blocking reagent to block possible remaining active sites and avoided the non-specific adsorption. In the presence of thrombin, the TBA binded to thrombin and the hemin released from the hemin/G-quadruplex electrocatalytic structure, increasing steric hindrance of the aptasensor and decomposing hemin/G-quadruplex electrocatalytic structure, which finally decreased the electrocatalytic efficiency of aptasensor toward H_2O_2 in the presence of NiHCFNPs with a decreased electrochemical signal. On the basis of the synergistic amplifying action, a detection limit as low as 2 pM for thrombin was obtained.
机译:一个简单的电化学适体传感器,用于凝血酶的灵敏检测,用G-四倍体辣根过氧化物酶模拟DNAzyme(hemin / G-四倍体系统)和阻断试剂-辣根过氧化物酶作为双重信号放大方案。首先将金纳米颗粒(nano-Au)电沉积在单壁纳米管(SWNT)-石墨烯修饰的电极表面上,以固定六氰合铁酸镍纳米颗粒(NiHCFNPs)的电化学探针。随后,电沉积另一个纳米Au层,以进一步固定凝血酶适体(TBA),后者随后与血红素形成了血红素/ G-四链体系统。然后将辣根过氧化物酶(HRP)用作阻断剂,以阻断可能残留的活性位点并避免非特异性吸附。在凝血酶存在下,TBA与凝血酶结合,血红素从hemin / G-四链体电催化结构中释放出来,增加了适体传感器的空间位阻,并分解了hemin / G-四链体电催化结构,最终降低了适体传感器对aptasensor的电催化效率。 NiHCFNPs存在下,H_2O_2的电化学信号降低。基于协同放大作用,获得对于凝血酶的低至2pM的检测极限。

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