Dimalanta Eileen T, Lim Alex, Runnheim Rod, Lamers Casey, Churas Chris, Forrest Daniel K, de Pablo Juan J, Graham Michael D, Coppersmith Susan N, Goldstein Steve, Schwartz David C
Laboratory for Molecular and Computational Genomics, Department of Chemistry, and Laboratory of Genetics, University of Wisconsin-Madison, 425 Henry Mall, Madison, Wisconsin 53706, USA.
Anal Chem. 2004 Sep 15;76(18):5293-301. doi: 10.1021/ac0496401.
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.
单分子方法有望实现大规模、极其微小的集合体,以生成同样庞大的数据集。尽管微流控设备此前已被设计用于操控单个DNA分子,但它们所具备的许多功能并不适用于通常从细胞中提取的非常大的DNA分子。重要的是,此类微流控设备必须在一个集成系统内工作,以实现高通量生物或生化分析——这是任何旨在实现化学/生物界面的设备的一项关键指标,也是创建大型数据集以供后续分析所必需的。这里的挑战在于设计一种集成微流控设备,以控制大型DNA分子(长度可达数毫米)的沉积或延伸,该设备将作为生物/生化分析的通用平台,在一个包括大规模并行数据收集和分析的集成系统中发挥作用。我们采用的方法是使用复制成型技术构建硅橡胶设备,将定向、延伸的DNA分子一致地沉积到带电表面上,创建大规模单分子阵列,我们在一个能创建大型数据集的集成环境中对其进行物理和生化分析。通过限制性内切酶图谱分析和单个人类基因组DNA分子的鉴定,证明了该方法的整体有效性。