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A highly sensitive method for detection of protein based on inhibition of Ru(bpy)_3~(2+)/TPrA electrochemiluminescent system

机译:基于Ru(bpy)_3〜(2 +)/ TPrA电化学发光系统的抑制蛋白的高灵敏度检测方法

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摘要

The detection of proteins is very important in the study of biochemistry procedure, and electrochemiluminescence method is a very practical tool for the study of protein folding, structure and quantification. In this work, bovine serum albumin (BSA) and casein were found to be able to significantly quench the electrochemiluminescence (ECL) of Ru(bpy)_3~(2+)/TPrA system, based on which a highly sensitive approach for the detection of protein was proposed. Under the optimized conditions, the logarithmic plot of the inhibited ECL versus the concentration of BSA and casein were linear over the ranges of 1-30 μg/L and 0.1-1.6 μg/L, respectively. The corresponding limit of detection (LOD) was 0.45 μg/L for BSA and 0.026 μg/L for casein (S/N = 3). UV, ECL and fluorescence methods were used to investigate the mechanism of the inhibited ECL of (Ru(bpy)_3)~(2+)/TPrA/BSA system. A mechanism based on the formation of protein-(Ru(bpy)_3)~(2+) super molecule was proposed, which would prevent (Ru(bpy)_3)~(2+) from reaching the working electrode surface so that induced ECL quenching.
机译:蛋白质的检测在生物化学过程的研究中非常重要,电化学发光方法是研究蛋白质折叠,结构和定量的非常实用的工具。在这项工作中,发现牛血清白蛋白(BSA)和酪蛋白能够显着淬灭Ru(bpy)_3〜(2 +)/ TPrA系统的电化学发光(ECL),在此基础上,该方法是一种高度灵敏的检测方法提出蛋白质。在最佳条件下,抑制的ECL对BSA和酪蛋白浓度的对数曲线分别在1-30μg/ L和0.1-1.6μg/ L范围内呈线性关系。相应的BSA检测限(LOD)为0.45μg/ L,酪蛋白为0.026μg/ L(S / N = 3)。采用紫外,ECL和荧光方法研究了(Ru(bpy)_3)〜(2 +)/ TPrA / BSA体系抑制ECL的机理。提出了一种基于蛋白质-(Ru(bpy)_3)〜(2+)超分子形成的机制,该机制可以防止(Ru(bpy)_3)〜(2+)到达工作电极表面,从而导致ECL淬火。

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