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利用经纯化且具有强拉曼活性的金纳米粒子簇在磁珠下拉检测法中快速灵敏地检测细胞因子肿瘤坏死因子-α(tnf-α)。

Rapid and sensitive SERS detection of the cytokine tumor necrosis factor alpha (tnf-α) in a magnetic bead pull-down assay with purified and highly Raman-active gold nanoparticle clusters.

机构信息

National Center for Materials Service Safety, University of Science and Technology Beijing, Beijing, 100083, China.

Department of Chemistry, Center for Nanointegration Duisburg-Essen (CENIDE) and Center of Medical Biotechnology (ZMB), University of Duisburg-Essen, 45141, Essen, Germany.

出版信息

Anal Bioanal Chem. 2018 Sep;410(23):5993-6000. doi: 10.1007/s00216-018-1218-0. Epub 2018 Jun 30.

DOI:10.1007/s00216-018-1218-0
PMID:29959484
Abstract

Tumor necrosis factor alpha (TNF-α) is a cytokine with significance in early diagnosis of cardiovascular diseases, obesity and insulin resistance. We demonstrate the proof of concept for a rapid and sensitive detection of TNF-α using a magnetic bead pull-down assay in combination with surface-enhanced Raman scattering (SERS). The use of purified and highly SERS-active small clusters of gold nanoparticles (AuNP) provides the high sensitivity of the assay with a limit of detection of ca. 1 pg/mL. Continuous density gradient centrifugation was employed for separating the very bright silica-encapsulated AuNP dimers and trimers from the significantly weaker AuNP monomers. Negative control experiments with other cytokines (IL-6, IL-8) and bovine serum albumin (BSA) confirm the high specificity of the assay, but indicate also space for future improvements by further reducing non-specific binding between proteins and the SERS nanotags. The multiplexing potential of this SERS-based detection scheme is exemplarily demonstrated by using a set of three spectrally distinct and highly SERS-active AuNP clusters with unique spectral barcodes. Graphical abstract ᅟ.

摘要

肿瘤坏死因子-α(TNF-α)是一种细胞因子,在心血管疾病、肥胖和胰岛素抵抗的早期诊断中具有重要意义。我们通过磁珠下拉测定法与表面增强拉曼散射(SERS)结合,证明了使用该方法快速、灵敏检测 TNF-α 的原理。该方法使用纯化的、具有高度 SERS 活性的金纳米粒子(AuNP)小簇,检测限约为 1pg/mL,具有很高的灵敏度。连续密度梯度离心用于分离非常亮的二氧化硅包裹的 AuNP 二聚体和三聚体与明显较弱的 AuNP 单体。用其他细胞因子(IL-6、IL-8)和牛血清白蛋白(BSA)进行的阴性对照实验证实了该测定方法的高特异性,但也表明通过进一步减少蛋白质与 SERS 纳米标签之间的非特异性结合,未来仍有改进的空间。通过使用一组三个具有独特光谱条码的光谱明显不同且具有高度 SERS 活性的 AuNP 簇,该 SERS 检测方案的多重检测潜力得到了示例证明。

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