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A microfluidic system for large DNA molecule arrays

机译:用于大型DNA分子阵列的微流体系统

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Single molecule approaches offer the promise of large, exquisitely miniature ensembles for the generation of equally large data sets. Although microfluidic devices have previously been designed to manipulate single DNA molecules, many of the functionalities they embody are not applicable to very large DNA molecules, normally extracted from cells. Importantly, such microfluidic devices must work within an integrated system to enable high-throughput biological or biochemical analysis-a key measure of any device aimed at the chemical/biological interface and required if large data sets are to be created for subsequent analysis. The challenge here was to design an integrated microfluidic device to control the deposition or elongation of large DNA molecules (up to millimeters in length), which would serve as a general platform for biological/biochemical analysis to function within an integrated system that included massively parallel data collection and analysis. The approach we took was to use replica molding to construct silastic devices to consistently deposit oriented, elongated DNA molecules onto charged surfaces, creating massive single molecule arrays, which we analyzed for both physical and biochemical insights within an integrated environment that created large data sets. The overall efficacy of this approach was demonstrated by the restriction enzyme mapping and identification of single human genomic DNA molecules.
机译:单分子方法为生成同样大的数据集提供了大而精巧的微型组合的希望。尽管微流控设备先前已设计为可操纵单个DNA分子,但它们体现的许多功能不适用于通常从细胞中提取的非常大的DNA分子。重要的是,这种微流体设备必须在集成系统中工作,以实现高通量的生物或生化分析,这是任何针对化学/生物界面的设备的关键措施,如果要创建大量数据集以进行后续分析,则需要使用该微流体设备。这里的挑战是设计一个集成的微流控设备,以控制大DNA分子(最大长度为毫米)的沉积或伸长,这将成为生物学/生化分析的通用平台,以在包含大规模并行操作的集成系统中发挥作用数据收集和分析。我们采取的方法是使用复制成型来构建硅橡胶设备,以将定向的细长DNA分子始终沉积在带电的表面上,从而创建大量的单分子阵列,我们在创建大型数据集的集成环境中分析了物理和生化方面的见解。通过限制酶作图和鉴定单个人类基因组DNA分子证明了该方法的整体功效。

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