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双金属金-银纳米板阵列作为一种高活性 SERS 基底用于检测链霉亲和素/生物素组装体。

Bimetallic gold-silver nanoplate array as a highly active SERS substrate for detection of streptavidin/biotin assemblies.

机构信息

State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, PR China.

出版信息

Anal Chim Acta. 2013 Dec 17;805:95-100. doi: 10.1016/j.aca.2013.10.045. Epub 2013 Nov 4.

DOI:10.1016/j.aca.2013.10.045
PMID:24296148
Abstract

The silver-modified gold nanoplate arrays as bimetallic surface-enhanced Raman scattering (SERS) substrates were optimized for the surface-enhanced Raman detection of streptavidin/biotin monolayer assemblies. The bimetallic gold-silver nanoplate arrays were fabricated by coating silver nanoparticles uniformly on the gold nanoplate arrays. Depending on silver nanoparticle coating, the localized surface plasmon resonance (LSPR) peak of the bimetallic gold-silver nanoplate arrays blue-shifted and broadened significantly. The common probe molecule, Niel Blue A sulfate (NBA) was used for testing the SERS activity of the bimetallic gold-silver nanoplate arrays. The SERS intensity increased with the silver nanoparticle coating, due to a large number of hot spots and nanoparticle interfaces. The platforms were tested against a monolayer of streptavidin functionalized over the bimetallic gold-silver nanoplate arrays showing that good quality spectra could be acquired with a short acquisition time. The supramolecular interaction between streptavidin (strep) and biotin showed subsequent modification of Raman spectra that implied a change of the secondary structure of the host biomolecule. And the detection concentration for biotin by this method was as low as 1.0 nM. The enhanced SERS performance of such bimetallic gold-silver nanoplate arrays could spur further interest in the integration of highly sensitive biosensors for rapid, nondestructive, and quantitative bioanalysis, particularly in microfluidics.

摘要

银修饰的金纳米板阵列作为双金属表面增强拉曼散射(SERS)基底,用于优化链霉亲和素/生物素单层组装的表面增强拉曼检测。通过在金纳米板阵列上均匀涂覆银纳米颗粒来制备双金属金银纳米板阵列。根据银纳米颗粒的涂覆情况,双金属金银纳米板阵列的局域表面等离子体共振(LSPR)峰发生明显的蓝移和展宽。常用的探针分子尼尔蓝 A 硫酸盐(NBA)用于测试双金属金银纳米板阵列的 SERS 活性。由于大量的热点和纳米颗粒界面,SERS 强度随银纳米颗粒的涂覆而增加。该平台用于测试双金属金银纳米板阵列上功能化的单层链霉亲和素,结果表明,通过短的采集时间可以获得高质量的光谱。链霉亲和素(strept)与生物素之间的超分子相互作用表明,拉曼光谱随后发生了变化,暗示了主体生物分子的二级结构发生了变化。并且该方法检测生物素的检测浓度低至 1.0 nM。这种双金属金银纳米板阵列的增强 SERS 性能可能会进一步激发对快速、无损和定量生物分析的高灵敏度生物传感器的集成研究,特别是在微流控领域。

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