A Novel Detection of Biomarker Molecule of α-synuclein for Parkinson Disease by Phospholipid Liposome-Immobilized Cantilever Biosensor Using Real-Time Quaking-Induced Conversion Method

R. Kobayashi, M. Noda, M. Sawamura, H. Yamakado, Masayuki Sohgawa
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引用次数: 4

Abstract

We newly applied real-time quaking-induced conversion (RT-QuIC) method for phospholipid liposome-immobilized cantilever sensor in order to obtain a trace amount of chronological behavior of α−synuclein (aSyn) as causative agent for Parkinson Disease. Our goal is to detect aggregated, not a monomeric, forms of aSyn in its initial stage, as it is most toxic in patient’s cerebrospinal fluid (CSF). Especially, by introducing similar processes of the RT-QuIC on a microscale cantilever surface, pM order aSyn fibril was detected, further indicating several hundreds of fM detection in the cantilever biosensor system that is fluorescent label-free technique.
基于实时振动诱导转换方法的磷脂脂质体-固定化悬臂式生物传感器检测帕金森病α-突触核蛋白生物标志物分子
为了获得作为帕金森病致病因子的α -突触核蛋白(aSyn)的痕量时序行为,我们采用实时振动诱导转换(RT-QuIC)方法对磷脂脂质体-固定化悬臂传感器进行了研究。我们的目标是在初始阶段检测聚合而非单体形式的aSyn,因为它在患者脑脊液(CSF)中毒性最大。特别是,通过在微尺度悬臂表面上引入RT-QuIC的类似过程,检测到pM阶的aSyn纤维,进一步表明在悬臂生物传感器系统中可以检测到数百种fM,这是一种无荧光标记技术。
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