Cockroft Scott L, Chu John, Amorin Manuel, Ghadiri M Reza
Department of Chemistry, The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
J Am Chem Soc. 2008 Jan 23;130(3):818-20. doi: 10.1021/ja077082c. Epub 2008 Jan 1.
The ability to monitor DNA polymerase activity with single-nucleotide resolution has been the cornerstone of a number of advanced single-molecule DNA sequencing concepts. Toward this goal, we report the first observation of the base-by-base DNA polymerase activity with single-base resolution at the single-molecule level. We describe the design and characterization of a supramolecular nanopore device capable of detecting up to nine consecutive DNA polymerase-catalyzed single-nucleotide primer extensions with high sensitivity and spatial resolution (<or=2.4 A). The device is assembled in a suspended lipid membrane by threading and mechanically capturing a single strand of DNA-PEG copolymer inside an alpha-hemolysin protein pore. Single-nucleotide primer extensions result in successive displacements of the template DNA strand within the protein pore, which can be monitored by the corresponding stepped changes in the ion current flowing through the pore under an applied transmembrane potential. The system described thus represents a promising advance toward nanopore-mediated single-molecule DNA sequencing concept and, in addition, might be applicable to studying a number of other biopolymer-protein interactions and dynamics.
以单核苷酸分辨率监测DNA聚合酶活性的能力一直是许多先进的单分子DNA测序概念的基石。为了实现这一目标,我们报告了在单分子水平上首次以单碱基分辨率逐个碱基观察DNA聚合酶活性。我们描述了一种超分子纳米孔装置的设计和特性,该装置能够以高灵敏度和空间分辨率(≤2.4 Å)检测多达九个连续的DNA聚合酶催化的单核苷酸引物延伸。该装置通过将单链DNA-PEG共聚物穿入并机械捕获在α-溶血素蛋白孔内,组装在悬浮脂质膜中。单核苷酸引物延伸导致模板DNA链在蛋白孔内连续位移,这可以通过在施加跨膜电位下流过孔的离子电流的相应阶梯变化来监测。因此,所描述的系统代表了纳米孔介导的单分子DNA测序概念的一个有前景的进展,此外,可能适用于研究许多其他生物聚合物-蛋白质相互作用和动力学。