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Enhancement of the Chemiluminescence Response of Enzymatic Reactions by Plasmonic Surfaces for Biosensing Applications

机译:等离子体表面增强酶反应的化学发光反应用于生物传感应用

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摘要

We report the enhancement of chemiluminescence response of horseradish peroxidase (HRP) in bioassays by plasmonic surfaces, which are comprised of (i) silver island films (SIFs) and (ii) metal thin films (silver, gold, copper, and nickel, 1 nm thick) deposited onto glass slides. A model bioassay, based on the interactions of avidin-modified HRP with a monolayer of biotinylated poly(ethylene-glycol)-amine, was employed to evaluate the ability of plasmonic surfaces to enhance chemiluminescence response of HRP. Chemiluminescence response of HRP in model bioassays were increased up to ~3.7-fold as compared to the control samples (i.e. glass slides without plasmonic nanoparticles), where the largest enhancement of the chemiluminescence response was observed on SIFs with high loading. These findings allowed us to demonstrate the use of SIFs (high loading) for the detection of a biologically relevant target protein (glial fibrillary acidic protein or GFAP), where the chemiluminescence response of the standard bioassay for GFAP was enhanced up to ~50% as compared to bioassay on glass slides.
机译:我们报告了通过等离子表面在生物测定中辣根过氧化物酶(HRP)的化学发光反应的增强,该表面由(i)银岛膜(SIF)和(ii)金属薄膜(银,金,铜和镍1纳米厚)沉积在载玻片上。基于亲和素修饰的HRP与生物素化的聚(乙二醇)-胺单层相互作用的模型生物测定法用于评估等离子体表面增强HRP化学发光反应的能力。与对照样品(即没有等离子纳米颗粒的载玻片)相比,模型生物测定中HRP的化学发光响应增加了约3.7倍,其中在高载量的SIF上观察到化学发光响应的最大增强。这些发现使我们能够证明使用SIF(高载量)检测生物学上相关的靶蛋白(胶质纤维酸性蛋白或GFAP),其中标准GFAP生物测定的化学发光反应可提高至约50%。与载玻片上的生物测定相比。

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