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用于原位结构生物学的冷冻聚焦离子束薄片制备方案。

Cryo-Focused Ion Beam Lamella Preparation Protocol for in Situ Structural Biology.

机构信息

CEITEC, Masaryk University, Brno, Czech Republic.

出版信息

Methods Mol Biol. 2021;2305:301-322. doi: 10.1007/978-1-0716-1406-8_15.

Abstract

The advances in electron cryo-microscopy have enabled high-resolution structural studies of vitrified macromolecular complexes in situ by cryo-electron tomography (cryo-ET). Since utilization of cryo-ET is generally limited to the specimens with thickness < 500 nm, a complex sample preparation protocol to study larger samples such as single eukaryotic cells by cryo-ET was developed and optimized over the last decade. The workflow is based on the preparation of a thin cellular lamella by cryo-focused ion beam milling (cryo-FIBM) from the vitrified cells. The sample preparation protocol is a multi-step process which includes utilization of several high-end instruments and comprises sample manipulation prone to sample deterioration. Here, we present a workflow for preparation of three different model specimens that was optimized to provide high-quality lamellae for cryo-ET or electron diffraction tomography with high reproducibility. Preparation of lamellae from large adherent mammalian cells, small suspension eukaryotic cell line, and protein crystals of intermediate size is described which represents examples of the most frequently studied samples used for cryo-FIBM in life sciences.

摘要

电子冷冻显微镜技术的进步使得通过冷冻电子断层扫描(cryo-ET)对玻璃态大分子复合物进行高分辨率结构研究成为可能。由于 cryo-ET 的应用通常限于厚度 < 500nm 的标本,因此过去十年中开发并优化了一种复杂的样品制备方案,以通过 cryo-ET 研究更大的样品,如单细胞真核细胞。该工作流程基于使用冷冻聚焦离子束铣削(cryo-FIBM)从玻璃态细胞中制备薄的细胞薄片。该样品制备方案是一个多步骤的过程,包括使用几种高端仪器,并包含易于导致样品恶化的样品操作。在这里,我们提出了一种用于制备三种不同模型标本的工作流程,该流程经过优化,可提供高质量的薄片,用于 cryo-ET 或电子衍射断层扫描,具有高重复性。描述了从大贴壁哺乳动物细胞、小悬浮真核细胞系和中等大小的蛋白质晶体制备薄片的过程,这些例子代表了生命科学中最常研究的用于 cryo-FIBM 的样品。

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