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Immunoassay readout method using extrinsic Raman labels adsorbed on immunogold colloids

机译:利用吸附在免疫金胶体上的外在拉曼标记的免疫分析读出方法

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An immunoassay readout method based on surface-enhanced Raman scattering (SERS) is described. The method exploits the SERS-derived signal from reporter molecules that are coimmobilized with biospecific species on gold colloids. This concept is demonstrated in a dual-analyte sandwich assay, in which two different antibodies covalently bound to a solid substrate specifically capture two different antigens from an aqueous sample. The captured antigens in turn bind selectively to their corresponding detection antibodies. The detection antibodies are conjugated with gold colloids that are labeled with different Raman reporter molecules, which serve as extrinsic labels for each type of antibody. The presence of a specific antigen is established by the characteristic SERS spectrum of the reporter molecule. A near-infrared diode laser was used to excite efficiently the SERS signal while minimizing fluorescence interference. We show that, by using different labels with little spectral overlap, two different antigenic species can be detected simultaneously. The potential of this concept to function as a readout strategy for multiple analytes is briefly discussed. [References: 42]
机译:描述了一种基于表面增强拉曼散射(SERS)的免疫分析读出方法。该方法利用了来自报告分子的SERS衍生信号,该报告分子与生物特异性物质共固定在金胶体上。在双重分析物夹心测定中证明了这一概念,其中两种共价结合至固体底物的不同抗体特异性地从水性样品中捕获两种不同的抗原。捕获的抗原又选择性地与其相应的检测抗体结合。检测抗体与金胶体缀合,金胶体用不同的拉曼报道分子标记,该拉曼报道分子用作每种类型抗体的外源标记。通过报告分子的特征SERS光谱确定特定抗原的存在。使用近红外二极管激光器可有效激发SERS信号,同时将荧光干扰降至最低。我们表明,通过使用几乎没有光谱重叠的不同标记,可以同时检测到两种不同的抗原物种。简要讨论了此概念作为多种分析物的读出策略的潜力。 [参考:42]

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