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