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Sensitive and inexpensive digital DNA analysis by microfluidic enrichment of rolling circle amplified single-molecules

机译:通过微循环富集滚环扩增单分子进行灵敏且廉价的数字DNA分析

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摘要

Single molecule quantification assays provide the ultimate sensitivity and precision for molecular analysis. However, most digital analysis techniques, i.e. droplet PCR, require sophisticated and expensive instrumentation for molecule compartmentalization, amplification and analysis. Rolling circle amplification (RCA) provides a simpler means for digital analysis. Nevertheless, the sensitivity of RCA assays has until now been limited by inefficient detection methods. We have developed a simple microfluidic strategy for enrichment of RCA products into a single field of view of a low magnification fluorescent sensor, enabling ultra-sensitive digital quantification of nucleic acids over a dynamic range from 1.2 aM to 190 fM. We prove the broad applicability of our analysis platform by demonstrating 5-plex detection of as little as ∼1 pg (∼300 genome copies) of pathogenic DNA with simultaneous antibiotic resistance marker detection, and the analysis of rare oncogene mutations. Our method is simpler, more cost-effective and faster than other digital analysis techniques and provides the means to implement digital analysis in any laboratory equipped with a standard fluorescent microscope.
机译:单分子定量分析为分子分析提供了最高的灵敏度和精确度。然而,大多数数字分析技术,即液滴PCR,需要复杂而昂贵的仪器来进行分子分隔,扩增和分析。滚圆放大(RCA)为数字分析提供了一种更简单的方法。然而,迄今为止,RCA分析的灵敏度一直受到效率低下的检测方法的限制。我们已经开发出了一种简单的微流控策略,可以将RCA产品富集到低倍荧光传感器的单一视野中,从而可以在1.2 aM至190 fM的动态范围内对核酸进行超灵敏的数字定量。我们通过演示同时检测抗生素抗性标记物的5个多重检测致病性DNA的约1 pg(约300个基因组拷贝),证明了我们的分析平台的广泛适用性,并分析了罕见的致癌基因突变。与其他数字分析技术相比,我们的方法更简单,更具成本效益且更快,并且为在配备标准荧光显微镜的任何实验室中实施数字分析提供了手段。

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