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Gold colloid-nanostructured surfaces for enhanced piezoelectric immunosensing of staphylococcal enterotoxin A

机译:金胶体纳米结构表面,用于增强葡萄球菌肠毒素A的压电免疫传感

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摘要

We describe the use of gold nanoparticles (AuNP) as a nanostructuring agent on quartz crystal sensor chips to engineer staphylococcal enterotoxin A (SEA) piezoelectric biosensors with amplified response. AuNPs were assembled on gold- or silicon-coated quartz crystal sensor chips by a wet chemistry process involving their chemisorption to preformed thiol and amine terminated Self-Assembled Monolayers (SAMs). The purpose of this nanostructuration was to modify the topography of the surface and improve the accessibility of the binding sites on the surface of the sensor chips. Biointerfaces, comprising a polyclonal antibody against staphylococcal enterotoxin A (SEA), were further built up on these gold nanoparticle-coated sensors and their ability to capture SEA were monitored in real time with a quartz crystal microbalance with dissipation monitoring. It was found out that, although the surface density in capture antibody was similar on both nanostructured and planar sensors, the sensor response, expressed as frequency shift recorded during the binding of SEA to the antibody, was significantly higher for the nanostructured sensors as compared to the planar ones. All the same, the limit of detection was lower for the nanostructured sensors: 8 ng/mL vs 20 ng/mL for the planar sensors. This was rationalized by a possibly better accessibility of the antigen binding sites rather than a consequence of specific surface increase. Using a sandwich type assay, gold nanoparticles coated silicon quartz sensor chips provided the lowest limit of detection of ca. 1 ng/mL in a total assay time of 25 min.
机译:我们描述了使用金纳米颗粒(AuNP)作为石英晶体传感器芯片上的纳米结构剂来工程化具有放大响应的葡萄球菌肠毒素A(SEA)压电生物传感器。 AuNP通过湿化学过程组装到金或硅涂层的石英晶体传感器芯片上,该过程涉及它们对预先形成的硫醇和胺封端的自组装单分子层(SAMs)的化学吸附作用。该纳米结构的目的是改变表面的形貌并改善传感器芯片表面上结合位点的可及性。在这些金纳米粒子涂层的传感器上进一步构建了包含抗葡萄球菌肠毒素A(SEA)多克隆抗体的生物界面,并通过石英晶体微量天平和耗散监测来实时监测其捕获SEA的能力。已发现,尽管纳米结构传感器和平面传感器中捕获抗体的表面密度相似,但与纳米结构传感器相比,传感器响应(表示为SEA与抗体结合过程中记录的频移)明显更高。平面的。相同的是,纳米结构传感器的检出限较低:8 ng / mL vs平面传感器为20 ng / mL。通过抗原结合位点可能更好的可及性而不是特异性表面增加的结果来合理化。使用三明治式测定法,金纳米粒子涂层硅石英传感器芯片提供了大约最低的检出限。在25分钟的总分析时间内为1 ng / mL。

著录项

  • 来源
    《Sensors and Actuators 》 |2018年第2期| 1604-1613| 共10页
  • 作者单位

    Sorbonne Universites, UPMC Univ Paris 06, CNRS, Institut Parisien de Chimie Moleculaire (IPCM), 4 place Jussieu, F-75005 Paris, France,Sorbonne Universites, UPMC Univ Paris 06, CNRS, Laboratoire de Reactivite de Surface (LRS), UMR 7197,4 Place Jussieu, F-75005 Paris, France;

    Sorbonne Universites, UPMC Univ Paris 06, CNRS, Institut Parisien de Chimie Moleculaire (IPCM), 4 place Jussieu, F-75005 Paris, France;

    Sorbonne Universites, UPMC Univ Paris 06, CNRS, Laboratoire de Reactivite de Surface (LRS), UMR 7197,4 Place Jussieu, F-75005 Paris, France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Quartz crystal microbalance (QCM); Biosensor; Antibody; Gold nanoparticles; Staphylococcal enterotoxin a (SEA); Protein A;

    机译:石英晶体微量天平(QCM);生物传感器抗体;金纳米粒子;葡萄球菌肠毒素a(SEA);蛋白A;

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