Inman James T, Smith Benjamin Y, Hall Michael A, Forties Robert A, Jin Jing, Sethna James P, Wang Michelle D
Department of Physics, LASSP and ‡Howard Hughes Medical Institute, Cornell University , Ithaca, New York 14853, United States.
Nano Lett. 2014 Nov 12;14(11):6475-80. doi: 10.1021/nl503009d. Epub 2014 Oct 14.
Optical trapping is a powerful single molecule technique used to study dynamic biomolecular events, especially those involving DNA and DNA-binding proteins. Current implementations usually involve only one of stretching, unzipping, or twisting DNA along one dimension. To expand the capabilities of optical trapping for more complex measurements would require a multidimensional technique that combines all of these manipulations in a single experiment. Here, we report the development and utilization of such a novel optical trapping assay based on a three-branch DNA construct, termed a "Y structure". This multidimensional assay allows precise, real-time tracking of multiple configurational changes. When the Y structure template is unzipped under both force and torque, the force and extension of all three branches can be determined simultaneously. Moreover, the assay is readily compatible with fluorescence, as demonstrated by unzipping through a fluorescently labeled, paused transcription complex. This novel assay thus allows for the visualization and precision mapping of complex interactions of biomechanical events.
光镊是一种强大的单分子技术,用于研究动态生物分子事件,特别是那些涉及DNA和DNA结合蛋白的事件。目前的实现方式通常只涉及沿一个维度拉伸、解链或扭转DNA中的一种。要扩展光镊进行更复杂测量的能力,将需要一种在单个实验中结合所有这些操作的多维技术。在这里,我们报告了一种基于三分支DNA构建体(称为“Y结构”)的新型光镊检测方法的开发和应用。这种多维检测方法允许对多种构象变化进行精确、实时跟踪。当Y结构模板在力和扭矩作用下解链时,可以同时确定所有三个分支的力和伸长。此外,该检测方法很容易与荧光兼容,如通过荧光标记的暂停转录复合物进行解链所证明的那样。因此,这种新型检测方法允许对生物力学事件的复杂相互作用进行可视化和精确映射。