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Chip-scale bioassays based on surface-enhanced Raman scattering: fundamentals and applications

机译:基于表面增强拉曼散射的芯片级生物测定:原理和应用

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摘要

This work explores the development and application of chip-scale bioassays based on surface-enhanced Raman scattering (SERS) for high throughput and high sensitivity analysis of biomolecules;The size effect of gold nanoparticles on the intensity of SERS is first presented. A sandwich immunoassay was performed using Raman-labeled immunogold nanoparticles with various sizes. The SERS responses were correlated to particle densities, which were obtained by atomic force microscopy (AFM). The response of individual particles was also investigated using Raman-microscope and an array of gold islands on a silicon substrate. The location and the size of individual particles were mapped using AFM;The next study describes a low-level detection of Escherichia coli O157:H7 and simulants of biological warfare agents in a sandwich immunoassay format using SERS labels, which have been termed Extrinsic Raman labels (ERLs). A new ERL scheme based on a mixed monolayer is also introduced. The mixed monolayer ERLs were created by covering the gold nanoparticles with a mixture of two thiolates, one thiolate for covalently binding antibody to the particle and the other thiolate for producing a strong Raman signal;An assay platform based on mixed self-assembled monolayers (SAMs) on gold is then presented. The mixed SAMs were prepared from dithiobis(succinimidyl undecanoate) (DSU) to covalently bind antibodies on gold substrate and oligo(ethylene glycol)-terminated thiol to prevent nonspecific adsorption of antibodies. After the mixed SAMs surfaces, formed from various mole fraction of DSU were incubated with antibodies, AFM was used to image individual antibodies on the surface;The final study presents a collaborative work on the single molecule adsorption of YOYO-I labeled lambda-DNA at compositionally patterned SAMs using total internal reflection fluorescence microscopy. The role of solution pH, lambda-DNA concentration, and domain size was investigated. This work also revealed the potential importance of structural defects.
机译:这项工作探索了基于表面增强拉曼散射(SERS)的芯片规模生物测定法在生物分子的高通量和高灵敏度分析中的开发和应用;首先提出了金纳米粒子的尺寸效应对SERS强度的影响。使用具有各种尺寸的拉曼标记的免疫金纳米颗粒进行夹心免疫测定。 SERS响应与通过原子力显微镜(AFM)获得的颗粒密度相关。还使用拉曼显微镜和硅衬底上的金岛阵列研究了单个颗粒的响应。使用原子力显微镜(AFM)绘制单个颗粒的位置和大小;下一研究描述了使用SERS标记的夹心免疫测定法对大肠杆菌O157:H7的低水平检测以及生物战剂的模拟物,这些标记被称为外在拉曼标记(ERL)。还介绍了一种基于混合单层的新ERL方案。混合的单层ERL是通过用两种硫醇盐的混合物覆盖金纳米颗粒而形成的,一种硫醇盐用于将抗体与粒子共价结合,另一种硫醇盐用于产生强拉曼信号;基于混合自组装单层(SAMs)的测定平台),然后呈现在黄金上。混合SAM由二硫代双(琥珀酸十一烷基琥珀酰亚胺酯)(DSU)制备,以共价结合金底物上的抗体和寡聚(乙二醇)端基的硫醇,以防止抗体的非特异性吸附。将由DSU的不同摩尔分数形成的混合SAMs表面与抗体孵育后,使用AFM对表面上的单个抗体进行成像;最终研究提出了在YOYO-I标记的lambda-DNA单分子吸附上的协同工作。使用全内反射荧光显微镜观察组成图案的SAM。研究了溶液pH,λ-DNA浓度和域大小的作用。这项工作还揭示了结构缺陷的潜在重要性。

著录项

  • 作者

    Park, Hye-Young;

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  • 年度 2005
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  • 原文格式 PDF
  • 正文语种 en
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