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首页> 外文期刊>Bulletin of the Korean Chemical Society >Single C-Reactive Protein Molecule Detection on a Gold-Nanopatterned Chip Based on Total Internal Reflection Fluorescence
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Single C-Reactive Protein Molecule Detection on a Gold-Nanopatterned Chip Based on Total Internal Reflection Fluorescence

机译:基于全内反射荧光的金纳米图案芯片上的单C反应蛋白分子检测

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Single C-reactive protein (CRP) molecules, which are non-specific acute phase markers and products of the innate immune system, were quantitatively detected on a gold-nanopatterned biochip using evanescent fieldenhanced fluorescence imaging. The 4 × 5 gold-nanopatterned biochip (spot diameter of 500 nm) was fabricated by electron beam nanolithography. Unlabeled CRP molecules in human serum were identified with single-molecule sandwich immunoassay by detecting secondary fluorescence generated by total internal reflection fluorescence (TIRF) microscopy. With decreased standard CRP concentrations, relative fluorescence intensities reduced in the range of 33.3 zM-800 pM. To enhance fluorescence intensities in TIRF images, the distance between biochip surface and CRP molecules was optimally adjusted by considering the quenching effect of gold and the evanescent field intensity. As a result, TIRF only detected one single-CRP molecule on the biochip the first time.
机译:单个C反应蛋白(CRP)分子是非特异性急性阶段标志物和先天免疫系统的产物,使用using逝场增强荧光成像技术在金纳米片生物芯片上进行了定量检测。通过电子束纳米光刻技术制造了4×5金纳米图案生物芯片(光斑直径为500 nm)。通过检测由全内反射荧光(TIRF)显微镜产生的次级荧光,用单分子夹心免疫测定法鉴定了人血清中未标记的CRP分子。随着标准CRP浓度的降低,相对荧光强度降低了33.3 zM-800 pM。为了增强TIRF图像中的荧光强度,可通过考虑金的猝灭效应和van逝场强度来最佳地调整生物芯片表面与CRP分子之间的距离。结果,TIRF首次仅在生物芯片上检测到一个单一CRP分子。

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