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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 >Graphene sheets, polyaniline and AuNPs based DNA sensor for electrochemical determination of BCR/ABL fusion gene with functional hairpin probe
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Graphene sheets, polyaniline and AuNPs based DNA sensor for electrochemical determination of BCR/ABL fusion gene with functional hairpin probe

机译:基于石墨烯片,聚苯胺和AuNPs的DNA传感器,用于使用功能性发夹探针电化学测定BCR / ABL融合基因

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A sensitive and selective electrochemical DNA sensor was developed for the detection of BCR/ABL fusion gene in chronic myelogenous leukemia (CML). Firstly, graphene sheets (GS) suspension was prepared with the aid of chitosan (CS) solution and then fabricated onto the glassy carbon electrode (GCE), followed by the electro-polymerization of aniline to form the PANI layer, then, Au nanoparticles (AuNPs) were electro-deposited onto the modified GCE to immobilize the capture probes. The capture probe employed a hairpin structure and dually labeled with a 5'-SH and a 3'-biotin. After hybridization with the target DNA, hairpin structure was compelled to open and 3'-biotin was forced to stay away from the electrode surface. As a result, streptavidin-alkaline phosphatase (SA-AP) was covalently binded to the capture probe via biotin-avidin system. Reduction currents were then generated after catalyzing the hydrolysis of the electroinactive 1-naphthyl phosphate (1-NP) to 1-naphthol and monitored by differential pulse voltammetry (DPV). Under optimum conditions, the amperometric signals increased linearly with the target DNA concentrations (10. pM to 1000. pM), and the DNA sensor exhibited a detection limit as low as 2.11 pM (S/N=3) with an excellent differentiation ability, and the proposed method showed acceptable stability and reproducibility. It has been applied for assay of BCR/ABL fusion gene from real samples with satisfactory results.
机译:开发了一种灵敏且选择性的电化学DNA传感器,用于检测慢性粒细胞性白血病(CML)中的BCR / ABL融合基因。首先,借助壳聚糖(CS)溶液制备石墨烯片(GS)悬浮液,然后将其制备到玻璃碳电极(GCE)上,然后进行苯胺的电聚合以形成PANI层,然后形成金纳米颗粒(将AuNPs电沉积到修饰的GCE上以固定捕获探针。捕获探针采用发夹结构,并用5'-SH和3'-生物素双重标记。与目标DNA杂交后,迫使发夹结构打开,并迫使3'-生物素远离电极表面。结果,链霉亲和素碱性磷酸酶(SA-AP)通过生物素-亲和素系统共价结合至捕获探针。然后,在催化电惰性1-磷酸萘酯(1-NP)水解为1-萘酚后产生还原电流,并通过差分脉冲伏安法(DPV)进行监测。在最佳条件下,安培信号随目标DNA浓度(10. pM至1000. pM)线性增加,并且DNA传感器的检测限低至2.11 pM(S / N = 3),具有出色的区分能力,所提方法具有良好的稳定性和重现性。已用于实际样品中BCR / ABL融合基因的测定,结果令人满意。

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