Granéli Annette, Yeykal Caitlyn C, Prasad Tekkatte Krishnamurthy, Greene Eric C
Department of Biochemistry and Molecular Biophysics, Columbia University, New York, New York 10032, USA.
Langmuir. 2006 Jan 3;22(1):292-9. doi: 10.1021/la051944a.
An unappreciated aspect of many single-molecule techniques is the need for an inert surface to which individual molecules can be anchored without compromising their biological integrity. Here, we present new methods for tethering large DNA molecules to the surface of a microfluidic sample chamber that has been rendered inert by the deposition of a supported lipid bilayer. These methods take advantage of the "bio-friendly" environment provided by zwitterionic lipids, but still allow the DNA molecules to be anchored at fixed positions on the surface. We also demonstrate a new method for constructing parallel arrays of individual DNA molecules assembled at defined positions on a bilayer-coated, fused silica surface. By using total internal reflection fluorescence microscopy to visualize the arrays, it is possible to simultaneously monitor hundreds of aligned DNA molecules within a single field-of-view. These molecular arrays will significantly increase the throughput capacity of single-molecule, fluorescence-based detection methods by allowing parallel processing of multiple individual reaction trajectories.
许多单分子技术中一个未得到充分重视的方面是需要一个惰性表面,单个分子能够锚定在该表面上而不损害其生物学完整性。在此,我们展示了将大型DNA分子拴系到微流体样品腔表面的新方法,该样品腔通过沉积支撑脂质双层而变得惰性。这些方法利用了两性离子脂质提供的“生物友好”环境,但仍允许DNA分子锚定在表面的固定位置。我们还展示了一种构建单个DNA分子平行阵列的新方法,这些分子组装在双层涂层的熔融石英表面的特定位置。通过使用全内反射荧光显微镜观察这些阵列,可以在单个视野内同时监测数百个排列的DNA分子。这些分子阵列将通过允许对多个单独反应轨迹进行并行处理,显著提高基于荧光的单分子检测方法的通量能力。