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Direct quantitative analysis of HCV RNA by atomic force microscopy without labeling or amplification

机译:通过原子力显微镜直接定量分析HCV RNA无需标记或扩增

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摘要

Force-based atomic force microscopy (AFM) was used to detect HCV (hepatitis C virus) RNA directly and to quantitatively analyse it without the need for reverse transcription or amplification. Capture and detection DNA probes were designed. The former was spotted onto a substrate with a conventional microarrayer, and the latter was immobilized on an AFM probe. To control the spacing between the immobilized DNAs on the surface, dendron self-assembly was employed. Force–distance curves showed that the mean force of the specific unbinding events was 32 ± 5 pN, and the hydrodynamic distance of the captured RNA was 30–60 nm. Adhesion force maps were generated with criteria including the mean force value, probability of obtaining the specific curves and hydrodynamic distance. The maps for the samples whose concentrations ranged from 0.76 fM to 6.0 fM showed that cluster number has a linear relationship with RNA concentration, while the difference between the observed number and the calculated one increased at low concentrations. Because the detection limit is expected to be enhanced by a factor of 10 000 when a spot of 1 micron diameter is employed, it is believed that HCV RNA of a few copy numbers can be detected by the use of AFM.
机译:基于力的原子力显微镜(AFM)用于直接检测HCV(丙型肝炎病毒)RNA,并进行定量分析,而无需进行逆转录或扩增。设计了捕获和检测DNA探针。用常规微阵列仪将前者点样到基质上,然后将后者固定在AFM探针上。为了控制表面上固定的DNA之间的间隔,采用了树枝状分子自组装。力-距离曲线显示,特定解离事件的平均力为32±5 pN,捕获的RNA的流体动力学距离为30-60 nm。以包括平均力值,获得特定曲线的可能性和流体动力距离的标准生成粘附力图。浓度范围为0.76 fM至6.0 fM的样品图谱显示,簇数与RNA浓度呈线性关系,而在低浓度下,观察到的数与计算出的数之间的差增加。因为当使用1微米直径的斑点时预期将检测限提高1万倍,所以相信可以通过使用AFM来检测几个拷贝数的HCV RNA。

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