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束缚粒子运动:一种探测DNA拓扑结构及与转录因子相互作用的简便技术。

Tethered Particle Motion: An Easy Technique for Probing DNA Topology and Interactions with Transcription Factors.

作者信息

Kovari Daniel T, Yan Yan, Finzi Laura, Dunlap David

机构信息

Department of Physics, Emory University, 400 Dowman Dr, Atlanta, GA, 30322, USA.

出版信息

Methods Mol Biol. 2018;1665:317-340. doi: 10.1007/978-1-4939-7271-5_17.

Abstract

Tethered Particle Motion (TPM) is a versatile in vitro technique for monitoring the conformations a linear macromolecule, such as DNA, can exhibit. The technique involves monitoring the diffusive motion of a particle anchored to a fixed point via the macromolecule of interest, which acts as a tether. In this chapter, we provide an overview of TPM, review the fundamental principles that determine the accuracy with which effective tether lengths can be used to distinguish different tether conformations, present software tools that assist in capturing and analyzing TPM data, and provide a protocol which uses TPM to characterize lac repressor-induced DNA looping. Critical to any TPM assay is the understanding of the timescale over which the diffusive motion of the particle must be observed to accurately distinguish tether conformations. Approximating the tether as a Hookean spring, we show how to estimate the diffusion timescale and discuss how it relates to the confidence with which tether conformations can be distinguished. Applying those estimates to a lac repressor titration assay, we describe how to perform a TPM experiment. We also provide graphically driven software which can be used to speed up data collection and analysis. Lastly, we detail how TPM data from the titration assay can be used to calculate relevant molecular descriptors such as the J factor for DNA looping and lac repressor-operator dissociation constants. While the included protocol is geared toward studying DNA looping, the technique, fundamental principles, and analytical methods are more general and can be adapted to a wide variety of molecular systems.

摘要

系留粒子运动(TPM)是一种通用的体外技术,用于监测线性大分子(如DNA)可能呈现的构象。该技术涉及监测通过感兴趣的大分子(作为系链)锚定到固定点的粒子的扩散运动。在本章中,我们概述了TPM,回顾了决定有效系链长度用于区分不同系链构象的准确性的基本原理,介绍了有助于捕获和分析TPM数据的软件工具,并提供了一种使用TPM表征乳糖阻遏物诱导的DNA环化的方案。任何TPM测定的关键是理解必须观察粒子扩散运动的时间尺度,以便准确区分系链构象。将系链近似为胡克弹簧,我们展示了如何估计扩散时间尺度,并讨论了它与区分系链构象的置信度的关系。将这些估计应用于乳糖阻遏物滴定测定,我们描述了如何进行TPM实验。我们还提供了图形驱动的软件,可用于加快数据收集和分析。最后,我们详细说明了滴定测定的TPM数据如何用于计算相关的分子描述符,如DNA环化的J因子和乳糖阻遏物-操纵子解离常数。虽然所包含的方案旨在研究DNA环化,但该技术、基本原理和分析方法更具通用性,可适用于多种分子系统。

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