血红素
适体
葡萄糖氧化酶
化学
组合化学
生物传感器
催化作用
辣根过氧化物酶
检出限
胶体金
过氧化物酶
线性范围
选择性
纳米颗粒
脱氧核酶
电化学气体传感器
电化学
氧化还原
循环伏安法
过氧化氢
电极
介电谱
安培法
色谱法
酶
生物化学
血红素
物理化学
生物
遗传学
作者
Xingxing Zhou,Song Guo,Jiaxi Gao,Jun Zhao,Shuwen Xue,Wenju Xu
标识
DOI:10.1016/j.bios.2017.06.039
摘要
Based on cascade catalysis amplification driven by glucose oxidase (GOx), a sensitive electrochemical impedimetric aptasensor for protein (carcinoembryonic antigen, CEA as tested model) was proposed by using Cu-based metal-organic frameworks functionalized with Pt nanoparticles, aptamer, hemin and GOx ([email protected]). CEA aptamer loaded onto [email protected] was bound with hemin to form [email protected] (hGq) with mimicking peroxidase activity. Through sandwich-type reaction of target CEA and CEA aptamers (Apt1 and Apt2), the obtained [email protected] as signal transduction probes (STPs) was captured to the modified electrode interface. When 3,3-diaminobenzidine (DAB) and glucose were introduced, the cascade reaction was initiated by GOx to catalyze the oxidation of glucose, in situ generating H2O2. Simultaneously, the decomposition of the generated H2O2 was greatly promoted by [email protected] and hGq as synergistic peroxide catalysts, accompanying with the significant oxidation process of DAB and the formation of nonconductive insoluble precipitates (IPs). As a result, the electron transfer in the resultant sensing interface was effectively hindered and the electrochemical impedimetric signal (EIS) was efficiently amplified. Thus, the high sensitivity of the proposed CEA aptasensor was successfully improved with 0.023 pg mL−1, which may be promising and potential in assaying certain clinical disease related to CEA.
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