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超高分辨率显微镜技术在细菌细胞中 DNA 结合蛋白的追踪研究

Super-Resolution Microscopy and Tracking of DNA-Binding Proteins in Bacterial Cells.

机构信息

Department of Biochemistry, University of Oxford, Oxford, UK.

出版信息

Methods Mol Biol. 2022;2476:191-208. doi: 10.1007/978-1-0716-2221-6_15.

Abstract

The ability to detect individual fluorescent molecules inside living cells has enabled a range of powerful microscopy techniques that resolve biological processes on the molecular scale. These methods have also transformed the study of bacterial cell biology, which was previously obstructed by the limited spatial resolution of conventional microscopy. In the case of DNA-binding proteins, super-resolution microscopy can visualize the detailed spatial organization of DNA replication, transcription, and repair processes by reconstructing a map of single-molecule localizations. Furthermore, DNA-binding activities can be observed directly by tracking protein movement in real time. This allows identifying subpopulations of DNA-bound and diffusing proteins, and can be used to measure DNA-binding times in vivo. This chapter provides a detailed protocol for super-resolution microscopy and tracking of DNA-binding proteins in Escherichia coli cells. The protocol covers the genetic engineering and fluorescent labeling of strains and describes data acquisition and analysis procedures, such as super-resolution image reconstruction, mapping single-molecule tracks, computing diffusion coefficients to identify molecular subpopulations with different mobility, and analysis of DNA-binding kinetics. While the focus is on the study of bacterial chromosome biology, these approaches are generally applicable to other molecular processes and cell types.

摘要

在活细胞内检测单个荧光分子的能力,使一系列强大的显微镜技术得以实现,这些技术可以在分子水平上解析生物过程。这些方法也改变了细菌细胞生物学的研究,因为传统显微镜的空间分辨率有限,之前的研究受到了阻碍。对于 DNA 结合蛋白,超分辨率显微镜可以通过重建单分子定位图谱来可视化 DNA 复制、转录和修复过程的详细空间组织。此外,通过实时跟踪蛋白质的运动,可以直接观察 DNA 结合活性。这可以识别 DNA 结合和扩散蛋白的亚群,并可用于测量体内 DNA 结合时间。本章提供了在大肠杆菌细胞中进行超分辨率显微镜和 DNA 结合蛋白追踪的详细方案。该方案涵盖了菌株的遗传工程和荧光标记,并描述了数据采集和分析程序,例如超分辨率图像重建、单分子轨迹映射、计算扩散系数以识别具有不同迁移率的分子亚群,以及 DNA 结合动力学分析。虽然重点是研究细菌染色体生物学,但这些方法通常适用于其他分子过程和细胞类型。

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