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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Fluorescence correlation spectroscopy of gold nanoparticles, and its application to an aptamer-based homogeneous thrombin assay
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Fluorescence correlation spectroscopy of gold nanoparticles, and its application to an aptamer-based homogeneous thrombin assay

机译:金纳米粒子的荧光相关光谱及其在基于适体的均相凝血酶测定中的应用

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We have studied the fluorescence properties and diffusion behaviors of gold nanoparticles (GNPs) in solution by using fluorescence correlation spectroscopy (FCS) at single molecule level. The GNPs display a high photo-saturation feature. Under illumination with strong laser light, they display higher brightness per particle (BPP) despite their low quantum yields. Based on the unique fluorescence properties and diffusion behaviors of GNPs, we have developed a sensitive and homogenous thrombin assay. It is based on a sandwich strategy and is making use of GNPs to which two different aptamers are conjugated. When the differently aptamer-labeled GNPs are mixed with solutions containing thrombin, the affinity reaction causes the GNPs to form dimers or oligomers. This leads to an increase in the diffusion time of the GNPs in the detection volume that is seen in FCS. The FCS method enables sensitive detection of the change in the characteristic diffusion time of the GNPs before and after the affinity reaction. Quantitative analysis of thrombin is based on the measurement of the change in the diffusion time. Under optimal conditions, the calibration plot is linear in the 0.5 nM to 110 nM thrombin concentration range, and the detection limit is 0.5 nM. The method was successfully applied to the direct determination of thrombin in human plasma.
机译:我们已经通过使用单分子水平的荧光相关光谱(FCS)研究了溶液中金纳米颗粒(GNP)的荧光性质和扩散行为。 GNP具有很高的光饱和度功能。在强激光照射下,尽管量子产率低,但它们仍显示出更高的每粒子亮度(BPP)。基于GNP的独特荧光性质和扩散行为,我们开发了一种敏感且均一的凝血酶测定法。它基于夹心策略,并利用GNP结合了两种不同的适体。当将不同的适体标记的GNP与含有凝血酶的溶液混合时,亲和反应会使GNP形成二聚体或低聚物。这导致了FCS中检测体积中GNP扩散时间的增加。通过FCS方法,可以灵敏地检测亲和反应前后GNP的特征扩散时间的变化。凝血酶的定量分析基于对扩散时间变化的测量。在最佳条件下,校准曲线在0.5 nM至110 nM凝血酶浓度范围内呈线性,检测极限为0.5 nM。该方法已成功应用于人体血浆中凝血酶的直接测定。

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