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用于研究扭转状态下转录的单分子角光学捕获

Single-Molecule Angular Optical Trapping for Studying Transcription Under Torsion.

作者信息

Ma Jie, Tan Chuang, Wang Michelle D

机构信息

School of Physics, Sun Yat-sen University, Guangzhou, People's Republic of China.

Laboratory of Atomic and Solid State Physics, Department of Physics, Cornell University, Ithaca, NY, USA.

出版信息

Methods Mol Biol. 2018;1805:301-332. doi: 10.1007/978-1-4939-8556-2_16.

Abstract

Optical tweezers are flexible and powerful single-molecule tools that have been extensively utilized in biophysical studies. With their ability to stretch and twist DNA, and measure its force and torque simultaneously, they provide excellent opportunities to gain novel insights into the function of protein motors and protein-DNA interactions. Recently, a novel DNA supercoiling assay using an angular optical tweezers (AOT) has been developed to investigate torque generation during transcription. Here, we provide a detailed and practical guide to performing this technique. Using bacterial RNA polymerase (RNAP) as an example, we present protocols for constructing and calibrating an AOT instrument, preparing DNA templates, and acquiring and analyzing real-time data for transcription under DNA supercoiling. While these protocols were initially developed with E. coli RNAP, they can be readily adapted to study other DNA-based motor proteins.

摘要

光镊是灵活且强大的单分子工具,已在生物物理研究中得到广泛应用。凭借其拉伸和扭转DNA并同时测量其力和扭矩的能力,光镊为深入了解蛋白质马达的功能以及蛋白质与DNA的相互作用提供了绝佳机会。最近,一种使用角向光镊(AOT)的新型DNA超螺旋测定法已被开发出来,用于研究转录过程中的扭矩产生。在此,我们提供了执行该技术的详细实用指南。以细菌RNA聚合酶(RNAP)为例,我们展示了构建和校准AOT仪器、制备DNA模板以及获取和分析DNA超螺旋条件下转录实时数据的方案。虽然这些方案最初是针对大肠杆菌RNAP开发的,但它们可以很容易地适用于研究其他基于DNA的马达蛋白。

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