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首页> 外文期刊>Analytica chimica acta >Fluorescence single-molecule counting assays for protein quantification using epi-fluorescence microscopy with quantum dots labeling
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Fluorescence single-molecule counting assays for protein quantification using epi-fluorescence microscopy with quantum dots labeling

机译:使用带有量子点标记的落射荧光显微镜进行蛋白质定量的荧光单分子计数测定

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A single-molecule counting approach for quantifying the antibody affixed to a surface using quantum dots and epi-fluorescence microscopy is presented. Modifying the glass substrates with carboxyl groups provides a hydrophilic surface that reacts with amine groups of an antibody to allow covalent immobilization of the antibody. Nonspecific adsorption of single molecules on the modified surfaces was first investigated. Then, quantum dots were employed to form complexes with surface-immobilized antibody molecules and used as fluorescent probes for single-molecule imaging. Epi-fluorescence microscopy was chosen as the tool for single-molecule fluorescence detection here. The generated fluorescence signals were taken by an electron multiplying charge-coupled device and were found to be proportional to the sample concentrations. Under optimal conditions, a linear response range of 5.0 x 10~(-14)-3.0 x 10~(-12) mol L~(-1) was obtained between the number of single molecules and sample concentration via a single-molecule counting approach.
机译:提出了一种使用量子点和落射荧光显微镜对附着在表面的抗体进行定量的单分子计数方法。用羧基修饰玻璃基板可提供与抗体的胺基反应的亲水表面,以实现抗体的共价固定。首先研究了单分子在改性表面上的非特异性吸附。然后,采用量子点与表面固定的抗体分子形成复合物,并将其用作单分子成像的荧光探针。 Epi荧光显微镜被选作此处的单分子荧光检测工具。产生的荧光信号由电子倍增电荷耦合装置获取,并与样品浓度成正比。在最佳条件下,通过单分子计数获得的单分子数量与样品浓度之间的线性响应范围为5.0 x 10〜(-14)-3.0 x 10〜(-12)mol L〜(-1)方法。

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