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Highly sensitive quantification of Alzheimers disease biomarkers by aptamer-assisted amplification

机译:适体辅助扩增对阿尔茨海默氏病生物标志物的高灵敏度定量

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摘要

Alzheimer's disease (AD), a chronic neurodegenerative disease associated with the loss of neurons in the brain, is the most pervasive type of dementia; 47 million people are affected, and the number is expected to increase to more than 131 million by 2050, according to Alzheimer's Disease International. Both early diagnosis and continuous monitoring are crucial for early intervention, symptomatic treatment, monitoring of the efficacy of intervention and improved patient function. Beta-amyloid peptide, tau, and phosphorylated tau are useful for screening and diagnosis; meanwhile, simultaneous assessment of multiple biomarkers is of paramount importance for accurate disease diagnosis.>Methods: Herein, we report a direct, inexpensive and ultrasensitive aptamer-based multiplex assay for the quantification of trace amounts of AD biomarkers in both human serum and cerebrospinal fluid (CSF) samples. In this newly developed assay, molecular recognition of an antibody-aptamer pair provides high specificity in target detection, and the use of a DNA amplification strategy affords high sensitivity, allowing quantification of AD biomarkers in both biological fluids in 1.5 h with only a diminutive amount of the sample consumed. A tailor-made turn-on fluorophore, namely, SPOH, was employed to label the antibody-aptamer hybrids and provide a strong fluorescence signal, which was then detected with a total internal reflection fluorescence microscopy electron-multiplying charge-coupled device (TIRFM-EMCCD) imaging system. The simultaneous detection of biomarkers was achieved by a direct shape-coded method in which the nanoplatforms can be distinguished from one another by their morphologies.>Results: This assay demonstrated a lower detection limit (in the femtomolar range) for AD biomarkers than the previously reported antibody-antibody method.>Conclusion: The developed assay holds tremendous clinical potential for early diagnosis of AD and monitoring of its progression.
机译:阿尔茨海默氏病(AD)是一种与大脑神经元丢失有关的慢性神经退行性疾病,是最普遍的痴呆类型。根据阿尔茨海默氏病国际组织的统计,有4700万人受到影响,预计到2050年,这一数字将增加到超过1.31亿。早期诊断和持续监测对于早期干预,对症治疗,监测干预效果和改善患者功能至关重要。 β-淀粉样肽,tau和磷酸化的tau可用于筛查和诊断;同时,同时评估多种生物标志物对于准确诊断疾病至关重要。>方法:本文中,我们报道了一种直接,廉价和超灵敏的基于适体的多重分析方法,用于定量分析痕量的AD生物标志物。人血清和脑脊液(CSF)样品。在这种新开发的检测方法中,抗体-适体对的分子识别在靶标检测中提供了高特异性,而DNA扩增策略的使用则提供了高灵敏度,从而允许在1.5 h内对两种生物液中的AD生物标志物进行定量,而仅需少量即可所消耗的样本中。使用量身定制的开启荧光团SPOH标记抗体-适体杂交体并提供强荧光信号,然后用全内反射荧光显微镜电子倍增电荷耦合器件(TIRFM- EMCCD)成像系统。生物标志物的同时检测是通过一种直接的形状编码方法实现的,其中纳米平台可以通过其形态相互区分。>结果:该测定法显示出较低的检测限(在飞摩尔范围内) >结论:该开发的测定法具有AD早期诊断和监测其进展的巨大临床潜力。

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