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原子力显微镜在 DNA 转录的单分子研究中的应用。

Single-molecule studies of DNA transcription using atomic force microscopy.

机构信息

School of Physics and Astronomy, University of Leeds, Woodhouse Lane, Leeds, West Yorkshire LS2 9JT, UK.

出版信息

Phys Biol. 2012;9(2):021001. doi: 10.1088/1478-3975/9/2/021001. Epub 2012 Apr 3.

DOI:10.1088/1478-3975/9/2/021001
PMID:22473059
Abstract

Atomic force microscopy (AFM) can detect single biomacromolecules with a high signal-to-noise ratio on atomically flat biocompatible support surfaces, such as mica. Contrast arises from the innate forces and therefore AFM does not require imaging contrast agents, leading to sample preparation that is relatively straightforward. The ability of AFM to operate in hydrated environments, including humid air and aqueous buffers, allows structure and function of biological and biomolecular systems to be retained. These traits of the AFM are ensuring that it is being increasingly used to study deoxyribonucleic acid (DNA) structure and DNA-protein interactions down to the secondary structure level. This report focuses in particular on reviewing the applications of AFM to the study of DNA transcription in reductionist single-molecule bottom-up approaches. The technique has allowed new insights into the interactions between ribonucleic acid (RNA) polymerase to be gained and enabled quantification of some aspects of the transcription process, such as promoter location, DNA wrapping and elongation. More recently, the trend is towards studying the interactions of more than one enzyme operating on a single DNA template. These methods begin to reveal the mechanics of gene expression at the single-molecule level and will enable us to gain greater understanding of how the genome is transcribed and translated into the proteome.

摘要

原子力显微镜(AFM)可以在原子级平坦的生物相容性支持表面(如云母)上检测具有高信噪比的单个生物大分子。对比度源于固有力,因此 AFM 不需要成像对比剂,从而导致相对简单的样品制备。AFM 能够在水合环境中(包括潮湿空气和水缓冲液)运行,允许保留生物和生物分子系统的结构和功能。这些 AFM 的特点确保了它越来越多地用于研究脱氧核糖核酸(DNA)结构和 DNA-蛋白质相互作用,直至二级结构水平。本报告特别侧重于审查 AFM 在简化的单分子从头开始方法中研究 DNA 转录的应用。该技术使人们对 RNA 聚合酶与 DNA 之间的相互作用有了新的认识,并能够量化转录过程的某些方面,如启动子位置、DNA 包装和延伸。最近,趋势是研究在单个 DNA 模板上操作的不止一种酶的相互作用。这些方法开始揭示单分子水平上基因表达的力学,并使我们能够更好地理解基因组如何转录并翻译成蛋白质组。

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