首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Hydrophobicity-driven self-assembly of protein and silver nanoparticles for protein detection using surface-enhanced Raman scattering
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Hydrophobicity-driven self-assembly of protein and silver nanoparticles for protein detection using surface-enhanced Raman scattering

机译:疏水性驱动的蛋白质和银纳米粒子的自组装,用于使用表面增强拉曼散射进行蛋白质检测

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摘要

Surface-enhanced Raman scattering (SERS) is a promising analytical technique for the detection and characterization of biological molecules and structures. The role of hydrophobic and hydrophilic surfaces in the self-assembly of protein-metallic nanoparticle structures for label-free protein detection is demonstrated. Aggregation is driven by both the hydrophobicity of the surface as well as the charge of the proteins. The best conditions for obtaining a reproducible SERS signal that allows for sensitive, label-free protein detection are provided by the use of hydrophobic surfaces and 16 × 10~(11) NPs per mL. A detection limit of approximately 0.5 μg mL~(-1) is achieved regardless of the proteins' charge properties and size. The developed method is simple and can be used for reproducible and sensitive detection and characterization of a wide variety of biological molecules and various structures with different sizes and charge status.
机译:表面增强拉曼散射(SERS)是用于检测和表征生物分子和结构的有前途的分析技术。疏水性和亲水性表面在无标记蛋白检测的蛋白金属纳米颗粒结构自组装中的作用得到了证明。聚集是由表面的疏水性以及蛋白质的电荷驱动的。通过使用疏水性表面和每毫升16×10〜(11)NPs,可获得获得可再现的SERS信号的最佳条件,该信号允许进行灵敏的无标记蛋白质检测。无论蛋白质的电荷性质和大小如何,检测限均约为0.5μgmL〜(-1)。所开发的方法简单,可用于具有不同大小和荷电状态的多种生物分子和各种结构的可再现和灵敏的检测和表征。

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