Meyer Nathan, Janot Jean-Marc, Torrent Joan, Balme Sébastien
Institut Européen des Membranes, UMR5635 University of Montpellier ENCSM CNRS, Place Eugène Bataillon, 34095 Montpellier cedex 5, France.
INM, University of Montpellier, INSERM, 34091 Montpellier, France.
ACS Cent Sci. 2022 Apr 27;8(4):441-448. doi: 10.1021/acscentsci.1c01404. Epub 2022 Feb 23.
The detection to α-synuclein (αS) assemblies as a biomarker of synucleinopathies is an important challenge for further development of an early diagnosis tool. Here, we present proof of concept real-time fast amyloid seeding and translocation (RT-FAST) based on a nanopipette that combines in one unique system a reaction vessel to accelerate the seed amplification and nanopore sensor for single-molecule αS assembly detection. RT-FAST allows the detection of the presence αS seeds WT and A53T variant in a given sample in only 90 min by adding a low quantity (35 μL at 100 nM) of recombinant αS for amplification. It also shows cross-seeding aggregation by adding mixing seeds A53T with WT monomers. Finally, we establish the dependence between the capture rate of aggregates by the nanopore sensor and the initial seed concentration from 200 pM to 2 pM, which promises further development toward a quantitative analysis of the initial seed concentration.
将α-突触核蛋白(αS)聚集体作为突触核蛋白病的生物标志物进行检测,是早期诊断工具进一步发展面临的一项重大挑战。在此,我们展示了基于纳米移液器的概念验证实时快速淀粉样蛋白播种与转运(RT-FAST),该系统在一个独特的体系中结合了用于加速种子扩增的反应容器和用于单分子αS聚集体检测的纳米孔传感器。通过添加少量(100 nM下35 μL)重组αS进行扩增,RT-FAST仅需90分钟就能检测给定样品中αS种子野生型(WT)和A53T变体的存在。通过将A53T与WT单体混合种子添加在一起,它还显示出交叉播种聚集。最后,我们确定了纳米孔传感器对聚集体的捕获率与200 pM至2 pM的初始种子浓度之间的依赖性,这为进一步发展对初始种子浓度的定量分析奠定了基础。