Sitters Gerrit, Laurens Niels, de Rijk Emilie J, Kress Holger, Peterman Erwin J G, Wuite Gijs J L
Department of Physics and Astronomy and LaserLaB, VU University Amsterdam, Amsterdam, The Netherlands.
Experimental Physics I, University of Bayreuth, Bayreuth, Germany; Department of Applied Physics, Eindhoven University of Technology, Eindhoven, The Netherlands.
Biophys J. 2016 Jan 5;110(1):44-50. doi: 10.1016/j.bpj.2015.11.028.
The ability to measure and manipulate single molecules has greatly advanced the field of biophysics. Yet, the addition of more single-molecule tools that enable one to measure in a parallel fashion is important to diversify the questions that can be addressed. Here we present optical pushing (OP), a single-molecule technique that is used to exert forces on many individual biomolecules tethered to microspheres using a single collimated laser beam. Forces ranging from a few femtoNewtons to several picoNewtons can be applied with a submillisecond response time. To determine forces exerted on the tethered particles by the laser, we analyzed their measured Brownian motion using, to our knowledge, a newly derived analytical model and numerical simulations. In the model, Brownian rotation of the microspheres is taken into account, which proved to be a critical component to correctly determine the applied forces. We used our OP technique to map the energy landscape of the protein-induced looping dynamics of DNA. OP can be used to apply loading rates in the range of 10(-4)-10(6) pN/s to many molecules at the same time, which makes it a tool suitable for dynamic force spectroscopy.
测量和操控单分子的能力极大地推动了生物物理学领域的发展。然而,增加更多能够实现并行测量的单分子工具对于丰富可解决的问题类型至关重要。在此,我们介绍光学推斥(OP),这是一种单分子技术,用于使用单束准直激光束对拴系在微球上的许多单个生物分子施加力。可以在亚毫秒响应时间内施加从几飞牛顿到几皮牛顿的力。为了确定激光对拴系粒子施加的力,我们使用了一个新推导的分析模型和数值模拟来分析测量到的布朗运动。在该模型中,考虑了微球的布朗旋转,这被证明是正确确定施加力的关键因素。我们使用OP技术绘制了蛋白质诱导的DNA环化动力学的能量景观。OP可用于同时对许多分子施加10^(-4)-10^(6) pN/s范围内的加载速率,这使其成为适用于动态力谱学的工具。