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首页> 外文期刊>Biotechnology and bioprocess engineering >Design, Synthesis, and Evaluation of Gold Nanoparticle-Antibody- Horseradish Peroxidase Conjugates for Highly Sensitive Chemiluminescence Immunoassay (hs-CLIA)
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Design, Synthesis, and Evaluation of Gold Nanoparticle-Antibody- Horseradish Peroxidase Conjugates for Highly Sensitive Chemiluminescence Immunoassay (hs-CLIA)

机译:金纳米颗粒-抗体-辣根过氧化物酶结合物的设计,合成和评估,用于高灵敏度化学发光免疫分析(hs-CLIA)

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摘要

Design and synthesis of a conjugate with high specificity and sensitivity constitutes a fundamental process for developing a highly sensitive immunoassay. In this study, we investigated the process of design, synthesis, and evaluation of gold nanoparticle (AuNP) conjugates that include both antibody and horseradish peroxidase (HRP) for application in a highly sensitive chemiluminescence immunoassay (hs-CLIA). To increase the labeling efficiency of HRP on the AuNP-based conjugates while maintaining process simplicity, two synthesis methods were suggested and evaluated using the physical adsorption-based conventional synthesis protocol. Specifically, the respective methods utilized adsorption or covalent coupling of aldehyde-activated (ald)HRP, which covalently binds to the primary amine group of a protein. The conjugates were characterized via spectroscopy and dynamic light scattering methods. Conjugate sensitivity was evaluated by not only analyzing the activity of HRP but also comparing the analytical sensitivity provided by the CL-based enzyme-linked immunosorbent assay for the detection of cardiac troponin I as a model target. Based on the results of this study, we demonstrated that the use of (ald)HRP for target labeling successfully enhanced the sensitivity of the AuNP-based conjugates; moreover, it could provide a promising labeling method for hs-CLIA.
机译:具有高特异性和敏感性的缀合物的设计和合成构成了开发高度灵敏的免疫测定的基本过程。在这项研究中,我们调查了设计,合成和评估金纳米粒子(AuNP)共轭物的过程,该共轭物包括抗体和辣根过氧化物酶(HRP),用于高灵敏度化学发光免疫分析(hs-CLIA)。为了提高在基于AuNP的结合物上HRP的标记效率,同时保持过程的简便性,提出了两种合成方法,并使用基于物理吸附的常规合成方案进行了评估。具体而言,相应的方法利用了醛活化的(ald)HRP的吸附或共价偶联,它与蛋白质的伯胺基共价结合。通过光谱学和动态光散射方法表征缀合物。不仅通过分析HRP的活性,而且通过比较基于CL的酶联免疫吸附测定法提供的分析敏感性来评估共轭敏感性,以检测作为模型靶标的心肌肌钙蛋白I。根据这项研究的结果,我们证明了使用(ald)HRP进行目标标记成功地提高了基于AuNP的结合物的敏感性。而且,它可以为hs-CLIA提供有希望的标记方法。

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