Chan Hei-Nga, Xu Di, Ho See-Lok, Wong Man Shing, Li Hung-Wing
Department of Chemistry , Hong Kong Baptist University , Hong Kong , China . Email:
Chem Sci. 2017 May 1;8(5):4012-4018. doi: 10.1039/c6sc05615f. Epub 2017 Mar 24.
Beta amyloid peptide, tau, and phosphorylated tau are well recognized as promising biomarkers for the diagnosis of Alzheimer's disease (AD). In this work, we developed a direct, versatile, and ultrasensitive multiplex assay for the quantification of trace amounts of these protein biomarkers for AD in different types of biological fluids including cerebrospinal fluid, serum, saliva, and urine. The detection assay is based on the immunoreaction between the target proteins and their corresponding pair of antibodies followed by fluorescence labelling with a newly developed indolium-based turn-on fluorophore, namely . was tailor-made as a reporter to provide a high signal-to-noise ratio for the detection assay. An exceptionally low limit of detection down to the femto-molar level was achieved in this assay with minute consumption of the sample. This versatile detection assay is capable of reliably quantifying not only the target proteins simultaneously from a CSF sample in an hour but also trace amounts of protein biomarkers in saliva and urine. This assay has a high potential to serve as a practical tool for the diagnosis of AD.
β淀粉样肽、tau蛋白和磷酸化tau蛋白是公认的用于阿尔茨海默病(AD)诊断的有前景的生物标志物。在这项工作中,我们开发了一种直接、通用且超灵敏的多重检测方法,用于定量不同类型生物流体(包括脑脊液、血清、唾液和尿液)中痕量的这些AD蛋白生物标志物。该检测方法基于目标蛋白与其相应抗体对之间的免疫反应,随后用新开发的基于吲哚鎓的开启型荧光团进行荧光标记,即 。 被特制为报告分子,为检测方法提供高信噪比。在该检测中,样品消耗极少,实现了低至飞摩尔水平的极低检测限。这种通用的检测方法不仅能够在一小时内从脑脊液样本中同时可靠地定量目标蛋白,还能定量唾液和尿液中的痕量蛋白生物标志物。该检测方法有很大潜力成为AD诊断的实用工具。