Picomolar Detection of Tau Protein Using 1D Photonic Crystal Biochips for Alzheimer's Disease Diagnosis

Alberto Sinibaldi, Francesco Chiavaioli, Agostino Occhicone, Norbert Danz, Peter Munzert, Francesco Baldini, Ambra Giannetti, Francesco Michelotti
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Abstract

Alzheimer's disease (AD) is a progressive neurological disorder that gradually impairs all cognitive functions. The diagnosis typically requires a combination of cognitive assessments, neuroimaging techniques, and biomarker analysis. In healthy neurons, Tau protein stabilizes microtubules, which are vital for maintaining the structure and proper functioning of nerve cells. However, elevated levels of Tau in cerebrospinal or other body fluids can be related to the progression of Alzheimer's disease. This study introduces an optical technique that employs a dual label-free and fluorescence operation mode to detect Tau protein in both standard running buffer and cerebrospinal fluid. This innovative method enables label-free analysis of the bio-conjugation process on biochips used for resolved fluorescence-based Tau detection. This work successfully demonstrates Tau protein detection in both matrixes, achieving an outstanding limit of detection of 2.4 pM in cerebrospinal fluid. Moreover, the analysis of the dose-response curve allows to estimate the dissociation constant (KD = 18 nM) for Tau interactions, yielding values that are in excellent agreement with existing literature using other techniques. These aspects highlight the added value of this technique, providing a valuable tool for investigating Alzheimer's-related biomarkers, as demonstrated in this study with Tau protein.

Abstract Image

利用一维光子晶体生物芯片进行Tau蛋白的皮摩尔检测用于阿尔茨海默病的诊断
阿尔茨海默病(AD)是一种进行性神经系统疾病,逐渐损害所有认知功能。诊断通常需要结合认知评估、神经成像技术和生物标志物分析。在健康的神经元中,Tau蛋白稳定微管,这对于维持神经细胞的结构和正常功能至关重要。然而,脑脊液或其他体液中Tau蛋白水平升高可能与阿尔茨海默病的进展有关。本研究介绍了一种采用无标记和荧光双重操作模式的光学技术,用于检测标准运行缓冲液和脑脊液中的Tau蛋白。这种创新的方法可以对生物芯片上的生物偶联过程进行无标记分析,用于解决基于荧光的Tau检测。这项工作成功地证明了Tau蛋白在两种基质中的检测,在脑脊液中达到了2.4 pM的检测极限。此外,对剂量-响应曲线的分析允许估计Tau相互作用的解离常数(KD = 18 nM),所得值与使用其他技术的现有文献非常一致。这些方面突出了该技术的附加价值,为研究阿尔茨海默病相关生物标志物提供了有价值的工具,正如本研究中Tau蛋白所证明的那样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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