首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Site-directed antibody immobilization using a protein A-gold binding domain fusion protein for enhanced SPR immunosensing
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Site-directed antibody immobilization using a protein A-gold binding domain fusion protein for enhanced SPR immunosensing

机译:使用蛋白A-金结合结构域融合蛋白进行定点抗体固定以增强SPR免疫感应

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摘要

We have implemented a novel strategy for the oriented immobilization of antibodies onto a gold surface based on the use of a fusion protein, the protein A-gold binding domain (PAG). PAG consists of a gold binding peptide (GBP) coupled to the immunoglobulin-binding domains of staphylococcal protein A. This fusion protein provides an easy and fast oriented immobilization of antibodies preserving its native structure, while leaving the antigen binding sites (Fab) freely exposed. Using this immobilization strategy, we have demonstrated the performance of the immunosensing of the human Growth Hormone by SPR. A limit of detection of 90 ng mL-1 was obtained with an inter-chip variability lower than 7%. The comparison of this method with other strategies for the direct immobilization of antibodies over gold surfaces has showed the enhanced sensitivity provided by the PAG approach.
机译:我们已经基于融合蛋白,即蛋白A-金结合域(PAG)的使用,实现了将抗体定向固定在金表面上的新策略。 PAG由金结合肽(GBP)和葡萄球菌蛋白A的免疫球蛋白结合域组成。这种融合蛋白可轻松快速地固定抗体,保持其天然结构,同时使抗原结合位点(Fab)自由暴露。使用这种固定策略,我们已经证明了SPR对人类生长激素的免疫感应性能。芯片间变异性低于7%,检测限为90 ng mL-1。该方法与将抗体直接固定在金表面上的其他策略的比较表明,PAG方法可提供更高的灵敏度。

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