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一种基于表面增强拉曼光谱的抗体-适配体夹心分析方法,用于使用金纳米颗粒检测细胞外囊泡相关的tau蛋白。

A SERS-Based Antibody-Aptamer Sandwich Assay for Extracellular Vesicle-Associated Tau Detection Using Gold Nanoparticles.

作者信息

Abdullah Saqer Al, Ghadami Samaneh, Khan Arifur Rahman, Ebrahimi Farbod, Nowlin Kyle, Ignatova Tetyana, Dellinger Kristen

机构信息

Department of Nanoengineering, Joint School of Nanoscience and Nanoengineering, North Carolina A&T State University, 2907 E Gate City Blvd, Greensboro, NC 27401.

Department of Nanoscience, Joint School of Nanoscience and Nanoengineering, University of North Carolina at Greensboro, 2907 E Gate City Blvd, Greensboro, NC 27401, USA.

出版信息

Adv Sens Res. 2025 Aug;4(8). doi: 10.1002/adsr.202500034. Epub 2025 Jun 12.

Abstract

Extracellular vesicles (EVs) have emerged as sources of promising, minimally invasive biomarkers for diagnosing and monitoring diseases like Alzheimer's. Using EVs as a source of biomarkers for neurological diseases is highly relevant because they can carry pathogenic proteins, such as tau and amyloid-β, across the blood-brain barrier and can be easily accessed and collected since they are available in almost all biofluids, including blood, urine, and saliva. Here, a bioanalytical antibody-aptamer sandwich assay detection using surface-enhanced Raman spectroscopy (SERS) is developed to quantify the expression of EV-associated tau. Specifically, a gold surface conjugated with antibodies was developed to capture tau protein derived from EVs. Subsequently, adding gold nanoparticles functionalized with SERS probes and aptamers enabled the detection of tau in EVs using SERS. The sensing platform exhibited excellent reproducibility, selectivity, and sensitivity for tau in a broad range of 30 pM-10 nM with a calculated detection limit of 13 pM. Detecting molecular targets within and on the surface of EVs can enable the design of multiplex biosensors for the early diagnosis of multifactorial diseases by simultaneously detecting and quantifying pathogenic proteins, such as amyloid-β and tau in Alzheimer's disease.

摘要

细胞外囊泡(EVs)已成为用于诊断和监测阿尔茨海默氏症等疾病的有前景的微创生物标志物来源。将EVs用作神经疾病的生物标志物来源具有高度相关性,因为它们可以携带诸如tau蛋白和淀粉样β蛋白等致病蛋白穿过血脑屏障,并且由于它们存在于几乎所有生物流体(包括血液、尿液和唾液)中,因此易于获取和收集。在此,开发了一种使用表面增强拉曼光谱(SERS)的生物分析抗体-适配体夹心测定法来定量EV相关tau的表达。具体而言,开发了一种与抗体缀合的金表面,以捕获源自EVs的tau蛋白。随后,添加用SERS探针和适配体功能化的金纳米颗粒,能够使用SERS检测EVs中的tau。该传感平台在30 pM - 10 nM的宽范围内对tau表现出优异的重现性、选择性和灵敏度,计算出的检测限为13 pM。检测EVs内部和表面的分子靶标能够通过同时检测和定量致病蛋白(如阿尔茨海默病中的淀粉样β蛋白和tau蛋白)来设计用于多因素疾病早期诊断的多重生物传感器。

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