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Angular-ratiometric plasmon-resonance based light scattering for bioaffinity sensing

机译:基于角速度等离子体激元共振的光散射用于生物亲和力传感

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We describe an exciting opportunity for affinity biosensing using a ratiometric approach to the angular-dependent light scattering from bioactivated and subsequently aggregated noble metal colloids. This new model sensing platform utilizes the changes in particle scattering from very small colloids, which scatter light according to traditional Rayleigh theory, as compared to the changes in scattering observed by much larger colloidal aggregates, formed due to a bioaffinity reaction. These larger aggregates no longer scatter incident light in a Cos(2) theta dependence, as is the case for Rayleigh scattering, but instead scatter light in an increased forward direction as compared to the incident geometry. By subsequently taking the ratio of the scattered intensity at two angles, namely 90 and 140, relative to the incident light, we can follow the association of biotinylated bovine serum albumin-coated 20 nm gold colloids, cross-linked by additions of streptavidin. This new model system can be potentially applied to many other nanoparticle assays and has many advantages over traditional fluorescence sensing and indeed light-scattering approaches. For example, a single nanoparticle can have the equivalent scattered intensity as 10(5) fluorescing fluorescein molecules substantially increasing detection; the angular distribution of scattered light from noble metal colloids is substantially easier to predict as compared to fluorescence; the scattered light is not quenched by biospecies; the ratiometric measurements described here are not dependent on colloid concentration as are other scattering techniques; and finally, the noble metal colloids are not prone to photodestruction, as is the case with organic fluorophores.
机译:我们描述了一种亲和力的生物传感的激动人心的机会,它使用比例方法从生物激活的随后聚集的贵金属胶体进行角度依赖性光散射。这个新的模型感测平台利用了非常小的胶体的颗粒散射变化,根据传统的瑞利理论,这些散射使光散射,而由于生物亲和反应而形成的更大的胶体聚集体所观察到的散射变化却与之不同。这些较大的聚集体不再像Rayleigh散射那样以Cos(2)theta依赖性来散射入射光,而是与入射几何体相比以增加的正向散射光。通过随后采用相对于入射光的两个角度(即90和140)的散射强度之比,我们可以观察到生物素化牛血清白蛋白涂层的20 nm金胶体的缔合,通过添加链霉亲和素进行交联。这种新的模型系统可以潜在地应用于许多其他的纳米颗粒测定,并且比传统的荧光传感和实际上的光散射方法具有许多优势。例如,单个纳米粒子可以具有与10(5)荧光素分子荧光相当的散射强度,从而大大提高检测效率;与荧光相比,贵金属胶体散射光的角分布基本上更容易预测;散射光不会被生物物种猝灭;这里描述的比例测量不像其他散射技术那样依赖胶体浓度。最后,贵金属胶体不像有机荧光团那样容易被光破坏。

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