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Force Spectroscopy with Dual-Trap Optical Tweezers: Molecular Stiffness Measurements and Coupled Fluctuations Analysis

机译:带有双阱光镊的力谱:分子刚度测量和耦合波动分析

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摘要

Dual-trap optical tweezers are often used in high-resolution measurements in single-molecule biophysics. Such measurements can be hindered by the presence of extraneous noise sources, the most prominent of which is the coupling of fluctuations along different spatial directions, which may affect any optical tweezers setup. In this article, we analyze, both from the theoretical and the experimental points of view, the most common source for these couplings in dual-trap optical-tweezers setups: the misalignment of traps and tether. We give criteria to distinguish different kinds of misalignment, to estimate their quantitative relevance and to include them in the data analysis. The experimental data is obtained in a, to our knowledge, novel dual-trap optical-tweezers setup that directly measures forces. In the case in which misalignment is negligible, we provide a method to measure the stiffness of traps and tether based on variance analysis. This method can be seen as a calibration technique valid beyond the linear trap region. Our analysis is then employed to measure the persistence length of dsDNA tethers of three different lengths spanning two orders of magnitude. The effective persistence length of such tethers is shown to decrease with the contour length, in accordance with previous studies.
机译:双陷阱光镊通常用于单分子生物物理学中的高分辨率测量。外部噪声源可能会阻碍此类测量,其中最突出的是沿不同空间方向的波动耦合,这可能会影响任何光镊的设置。在本文中,我们从理论和实验的角度分析了双阱光镊设置中这些耦合的最常见来源:阱和系链的未对准。我们提供了判别不同类型错位,估计其定量相关性并将其包括在数据分析中的标准。就我们所知,实验数据是通过直接测量力的新型双阱光镊装置获得的。在可以忽略不对准的情况下,我们提供了一种基于方差分析来测量陷阱和系链刚度的方法。可以将这种方法视为在线性陷阱区域以外有效的校准技术。然后,我们的分析用于测量跨越两个数量级的三个不同长度的dsDNA系链的持久长度。根据先前的研究,这种系绳的有效持续长度显示出随着轮廓长度而减小。

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