Supplementary Information files for Rapid quantification of prion proteins using resistive pulse sensing
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https://repository.lboro.ac.uk/articles/Supplementary_Information_files_for_Rapid_quantification_of_prion_proteins_using_resistive_pulse_sensing/12815774
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Supplementary Information files for Rapid quantification of prion proteins using resistive pulse sensing<br>Prion diseases are a group of fatal transmissible neurological conditions caused by the change in conformation of intrinsic cellular prion protein (PrPC). We present a rapid assay using aptamers and resistive pulse sensing, RPS, to extract and quantify PrPC from complex sample matrices. We functionalise the surface of superparamagnetic beads, SPBs, with a DNA aptamer. First SPB’s termed P-beads, are used to pre-concentrate the analyte from a large sample volume. The PrPC protein is then eluted from the P-beads before aptamer modified sensing beads, S-beads, are added. The velocity of the S-beads through the nanopore reveals the concentration of the<br>
本数据集为《基于电阻脉冲传感(resistive pulse sensing,RPS)快速定量朊蛋白》的补充信息文件。
朊病毒病是一类由内源性细胞朊蛋白(PrPC)构象改变所引发的致死性传染性神经系统疾病。本研究开发了一种结合适配体与电阻脉冲传感(RPS)的快速检测方法,可从复杂样品基质中提取并定量内源性细胞朊蛋白。
研究人员将DNA适配体修饰于超顺磁珠(SPBs)表面。首先将此类磁珠(命名为P磁珠)用于从大体积样品中预富集分析物,随后将结合于P磁珠上的PrPC蛋白洗脱,再加入适配体修饰的传感微珠(S-beads)。S-beads通过纳米孔时的运动速度可反映其浓度。
提供机构:
Loughborough University
创建时间:
2020-08-17



