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单分子荧光成像技术研究核蛋白复合物在 DNA 复制停顿位点的作用

Single-Molecule Fluorescence Imaging of DNA Replication Stalling at Sites of Nucleoprotein Complexes.

机构信息

Molecular Horizons and School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW, Australia.

Illawarra Health and Medical Research Institute, Wollongong, NSW, Australia.

出版信息

Methods Mol Biol. 2024;2694:215-234. doi: 10.1007/978-1-0716-3377-9_11.

Abstract

DNA replication in cells occurs on crowded and often damaged template DNA, forming potentially deleterious roadblocks to the progressing replication fork. Numerous tools have been developed to investigate the mechanisms of DNA replication and the fate of stalled replication forks. Here, we describe single-molecule fluorescence imaging methods to visualize processive DNA replication and replication fork stalling at site-specific nucleoprotein complexes. Using dCas9 as a protein barrier and rolling-circle DNA templates, we visualize effective, stable, and site-specific blocking of the Escherichia coli replisome. Additionally, we present a protocol to produce an 18-kb rolling-circle DNA template that provides increased spatial resolution in imaging the interplay between replisomes and roadblocks. These methods can be used to investigate encounters of the replisome with nucleoprotein complexes at the single-molecule level, providing important mechanistic details of replisome stalling and downstream rescue or restart pathways.

摘要

细胞中的 DNA 复制发生在拥挤且经常受损的模板 DNA 上,这会形成对前进的复制叉有潜在危害的障碍物。已经开发了许多工具来研究 DNA 复制的机制和停滞的复制叉的命运。在这里,我们描述了单分子荧光成像方法,以可视化特定核蛋白复合物处的连续 DNA 复制和复制叉停滞。使用 dCas9 作为蛋白质障碍和滚环 DNA 模板,我们可以有效地、稳定地且特异性地阻止大肠杆菌复制体。此外,我们还介绍了一种产生 18kb 滚环 DNA 模板的方案,该模板在成像复制体和障碍物之间的相互作用时提供了更高的空间分辨率。这些方法可用于在单分子水平上研究复制体与核蛋白复合物的相遇,为复制体停滞和下游挽救或重新启动途径提供重要的机制细节。

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