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Disturbance-free rapid solution exchange for magnetic tweezers single-molecule studies

机译:用于磁镊子单分子研究的无扰动快速溶液交换

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摘要

Single-molecule manipulation technologies have been extensively applied to studies of the structures and interactions of DNA and proteins. An important aspect of such studies is to obtain the dynamics of interactions; however the initial binding is often difficult to obtain due to large mechanical perturbation during solution introduction. Here, we report a simple disturbance-free rapid solution exchange method for magnetic tweezers single-molecule manipulation experiments, which is achieved by tethering the molecules inside microwells (typical dimensions–diameter (D): 40–50 μm, height (H): 100 μm; H:D∼2:1). Our simulations and experiments show that the flow speed can be reduced by several orders of magnitude near the bottom of the microwells from that in the flow chamber, effectively eliminating the flow disturbance to molecules tethered in the microwells. We demonstrate a wide scope of applications of this method by measuring the force dependent DNA structural transitions in response to solution condition change, and polymerization dynamics of RecA on ssDNA/SSB-coated ssDNA/dsDNA of various tether lengths under constant forces, as well as the dynamics of vinculin binding to α-catenin at a constant force (< 5 pN) applied to the α-catenin protein.
机译:单分子操作技术已被广泛应用于研究DNA和蛋白质的结构和相互作用。这些研究的一个重要方面是获得相互作用的动力。然而,由于溶液引入过程中的较大机械扰动,通常难以获得初始结合。在这里,我们报告了一种用于磁镊子单分子操作实验的简单,无干扰的快速溶液交换方法,该方法是通过将微孔内的分子束缚在一起(典型尺寸–直径(D):40–50μm,高度(H): 100μm; H:D〜2:1)。我们的仿真和实验表明,在微孔底部附近,流速可以比流动室中的流速降低几个数量级,从而有效消除了对微孔中束缚分子的流动干扰。我们通过测量响应溶液条件变化的力依赖性DNA结构转变以及恒定力作用下Reca在不同系链长度的ssDNA / SSB包覆的ssDNA / dsDNA上的聚合动力学,证明了该方法的广泛应用施加于α-catenin蛋白的恒定力(<5 pN)下长链蛋白结合α-catenin的动力学。

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