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Direct and multiplex quantification of protein biomarkers in serum samples using an immuno-magnetic platform

机译:使用免疫磁性平台直接和多重定量血清样品中的蛋白质生物标志物

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摘要

A direct and ultrasensitive multiplex assay using an immuno-magnetic platform has been developed for the quantification of trace amounts of circulating cancer-associated antigens in serum. The detection is based on the specific immuno-interactions among the target antigen, detection antibody and capture antibody that is immobilized on the surface of magnetic nanoparticles. The sandwiched immuno-assembly is then labelled with turn-on fluorophores and detected with a fluorescence imaging system. To afford a high signal-to-noise ratio, three turn-on fluorophores with unique optical properties have been designed and synthesized to label the target antigens. The developed assay has achieved a remarkable LOD down to the femto-molar regime without sample pre-treatment. This versatile assay can efficiently differentiate the target antigen from a protein matrix and simultaneously quantify multiple cancer-associated antigens, for instance, alpha-fetoprotein (AFP), carcinoembryonic antigen (CEA), and prostate specific antigen (PSA) using only 6 μL of serum sample in an hour. This novel system has a high applicability to serve as a universal and useful tool for early disease diagnostics.
机译:已经开发了使用免疫磁性平台的直接和超灵敏的多重测定法,用于定量测定血清中痕量的循环癌相关抗原。该检测基于固定在磁性纳米粒子表面的靶抗原,检测抗体和捕获抗体之间的特异性免疫相互作用。然后,将夹在中间的免疫组件用开启的荧光团标记,并用荧光成像系统进行检测。为了提供高信噪比,已经设计并合成了具有独特光学特性的三种开启荧光团以标记靶抗原。无需样品预处理,开发的测定方法甚至可以在毫微微摩尔比条件下实现出色的LOD。这种多功能的测定方法可以仅使用6μL的高效液相色谱就可以有效地从蛋白质基质中区分目标抗原,并同时定量多种与癌症相关的抗原,例如甲胎蛋白(AFP),癌胚抗原(CEA)和前列腺特异性抗原(PSA)。一小时内获得血清样本。这种新颖的系统具有很高的适用性,可以用作早期疾病诊断的通用和有用的工具。

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