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Voltammetric aptasensor combined with magnetic beads assay developed for detection of human activated protein C

机译:伏安适体传感器结合磁珠检测技术开发用于检测人活化蛋白C

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摘要

A sensitive and selective label free voltammetric aptasensor based on magnetic beads assay was performed for the first time in our study for monitoring of human activated protein C (APC), which is a serine protease (i.e., key enzyme of the protein C pathway). An amino modified DNA aptamer (DNA APT) was covalently immobilized onto the surface of carboxylated magnetic beads (MBs), and then, the specific interaction between DNA APT and its cognate protein, APC, was performed at the surface of MBs. Similarly a biotinylated DNA APT was immobilized onto the surface of streptavidin coated MBs. Before and after interaction process, the oxidation signal of guanine was measured at disposable pencil graphite electrode (PGE) surface in combination with differential pulse voltammetry (DPV) technique and accordingly, the decrease at the guanine signal was evaluated. The biomolecular recognition of APC was successfully achieved with a low detection limit found as 2.35 μg mL~(-1) by using MB-COOH based assay. Moreover, the selectivity of this aptasensor assay was tested in the presence of numerous proteins and other biomolecules: protein C (PC), thrombin (THR), bovine serum albumin (BSA), factor Va (FVa) and chromogenic substrate (KS).
机译:在我们的研究中首次进行了基于磁珠测定的灵敏且无选择性标记的伏安适体传感器,用于监测人激活蛋白C(APC),这是一种丝氨酸蛋白酶(即蛋白C途径的关键酶)。将氨基修饰的DNA适体(DNA APT)共价固定在羧化磁珠(MBs)的表面上,然后在MBs的表面进行DNA APT及其同源蛋白APC之间的特异性相互作用。类似地,将生物素化的DNA APT固定在链霉亲和素包被的MB的表面上。在相互作用过程之前和之后,结合差动脉冲伏安法(DPV)技术在一次性铅笔石墨电极(PGE)表面测量鸟嘌呤的氧化信号,并据此评估鸟嘌呤信号的减少。通过基于MB-COOH的检测,成功地实现了APC的生物分子识别,检测限低至2.35μgmL〜(-1)。此外,在多种蛋白质和其他生物分子的存在下测试了这种适体传感器测定的选择性:蛋白质C(PC),凝血酶(THR),牛血清白蛋白(BSA),因子Va(FVa)和生色底物(KS)。

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