细菌附属物的纯化和冷冻电镜分析。

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Juan C Sanchez, Joseph K Baumgardt, Elizabeth R Wright
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引用次数: 0

摘要

一些细胞外螺旋蛋白质聚合物对支持细菌的运动至关重要。细菌鞭毛是一种用于支持细胞运动的聚合物附属物。一直以来,对鞭毛和其他细丝的结构研究仅限于那些存在或锁定为伸直状态的细丝。在这里,我们介绍了一种强大的工作流程,它能产生与生物相关的细菌鞭毛细丝高分辨率冷冻电镜(cryo-EM)结构。我们重点介绍了一种简单的纯化方法,该方法以几个离心步骤为中心,利用新月褶杆菌的鞭毛丝弹射过程,分离出适合透射电子显微镜(TEM)研究的鞭毛丝。在对样品进行玻璃化处理以收集低温电子显微镜(cryo-EM)数据之前,先通过 SDS-PAGE 和阴性染色 TEM 分析验证样品的质量。我们提供了通过低温电子显微镜螺旋重建方法重建直的或弯曲的鞭毛细丝的详细方案,然后概述了模型的建立和验证。在我们手中,这一工作流程产生了多个低于 3 Å 分辨率的鞭毛结构,其中一个数据集的全局分辨率达到了 2.1 Å。这一工作流程的应用支持结构-功能研究,以更好地了解在生物相关状态下调节丝状结构的分子相互作用。未来的工作不仅将研究调控细菌鞭毛和其他菌丝组织的相互作用,还将为开发新的螺旋生物聚合物的生物技术应用奠定基础。主要特点 - 通过简单的细菌培养、离心和重悬浮方法,快速高质量地纯化细菌鞭毛。- 丝状物体的高通量冷冻电镜数据采集。- 使用 cryoSPARC 实现螺旋重建算法,生成细菌鞭毛或其他螺旋聚合物的高分辨率三维结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Purification and Cryo-Electron Microscopy Analysis of Bacterial Appendages.

A number of extracellular helical protein polymers are crucial for supporting bacterial motility. The bacterial flagellum is a polymeric appendage used to support cellular motility. Historically, structural studies of flagellar and other filaments were limited to those present as or locked into straightened states. Here, we present a robust workflow that produces biologically relevant high-resolution cryo-electron microscopy (cryo-EM) structures of bacterial flagellar filaments. We highlight how a simple purification method, centered around several centrifugation steps, exploits the process of filament ejection in Caulobacter crescentus and results in isolated filaments amenable to transmission electron microscopy (TEM) studies. The quality of the sample is validated by SDS-PAGE and negative stain TEM analysis before a sample is vitrified for cryogenic electron microscopy (cryo-EM) data collection. We provide a detailed protocol for reconstructing either straight or curved flagellar filaments by cryo-EM helical reconstruction methods, followed by an overview of model building and validation. In our hands, this workflow resulted in several flagellar structures below 3 Å resolution, with one data set reaching a global resolution of 2.1 Å. The application of this workflow supports structure-function studies to better understand the molecular interactions that regulate filament architecture in biologically relevant states. Future work will not only examine interactions that regulate bacterial flagellar and other filament organization but also provide a foundation for developing new helical biopolymers for biotech applications. Key features • Rapid high-quality purification of bacterial flagella via simple bacterial culturing, centrifugation, and resuspension methods. • High-throughput cryo-EM data collection of filamentous objects. • Use of cryoSPARC implementations of helical reconstruction algorithms to generate high-resolution 3D structures of bacterial flagella or other helical polymers.

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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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