假阳性悖论
化学
蛋白质聚集
低聚物
原位
小分子
组合化学
药物发现
纳米技术
Tau病理学
构造(python库)
生物物理学
分子探针
计算机科学
分子
τ蛋白
钥匙(锁)
分析物
分子动力学
纳米颗粒
聚集诱导发射
事件(粒子物理)
生物系统
计算生物学
药物靶点
作者
Yuanhao Wang,Jiangyu Wang,Hui Wang,Bintong Huang,Zhentao Zhang,Yueming Zhai
摘要
ABSTRACT The abnormal aggregation of tau into soluble oligomers is a key pathological event in tauopathies including Alzheimer's disease. Detection of tau oligomers remains challenging due to their dynamic and heterogeneous nature, as well as the lack of reliable strategies for validating aggregation‐active species. In this study, we construct a stable functionalized solid‐state nanonet detection platform to achieve in situ monitoring of the heparin‐induced stepwise growth aggregation of tau oligomers and the verification of drug‐induced growth inhibition. Based on this platform, we propose a “recognition‐verification” dual‐confirmation strategy for high‐specificity single‐molecule detection of tau oligomers. Surface‐immobilized antibodies achieve primary target capture, while the intrinsic aggregation behavior of captured molecules serves as secondary verification to reduce false positives arising from nontarget capture or nonspecific adsorption. Furthermore, by converting the electrochemical sensing to an optical readout, we demonstrate the potential applicability of this strategy in practical detection. This dual‐confirmation strategy helps address false‐positive signals associated with nonspecific molecular interactions, enabling real‐time analysis of protein aggregation and holding promise for early diagnosis and drug screening of tau‐related neurodegenerative diseases.
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