FAST-EM 阵列层析成像:多波束体电子显微镜工作流程。

Methods in microscopy Pub Date : 2024-07-11 eCollection Date: 2024-04-01 DOI:10.1515/mim-2024-0005
Arent J Kievits, B H Peter Duinkerken, Ryan Lane, Cecilia de Heus, Daan van Beijeren Bergen En Henegouwen, Tibbe Höppener, Anouk H G Wolters, Nalan Liv, Ben N G Giepmans, Jacob P Hoogenboom
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引用次数: 0

摘要

阐明组织和细胞的三维纳米级结构对于了解生物过程的复杂性至关重要。电子显微镜(EM)提供了可靠解释所需的分辨率,但电子显微镜有限的吞吐量阻碍了其对大体积进行有效成像的能力。FAST-EM是一种新型多束扫描透射电子显微镜,可通过64束电子束并行扫描样品来加快采集速度。FAST-EM 利用光学检测分离各个电子束的信号。演示了多个生物样本超微结构数据的采集和三维重建。结果表明,该工作流程能够生成具有高分辨率和高对比度的大体积重建数据,从而在可行的采集时限内解决生物研究问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FAST-EM array tomography: a workflow for multibeam volume electron microscopy.

Elucidating the 3D nanoscale structure of tissues and cells is essential for understanding the complexity of biological processes. Electron microscopy (EM) offers the resolution needed for reliable interpretation, but the limited throughput of electron microscopes has hindered its ability to effectively image large volumes. We report a workflow for volume EM with FAST-EM, a novel multibeam scanning transmission electron microscope that speeds up acquisition by scanning the sample in parallel with 64 electron beams. FAST-EM makes use of optical detection to separate the signals of the individual beams. The acquisition and 3D reconstruction of ultrastructural data from multiple biological samples is demonstrated. The results show that the workflow is capable of producing large reconstructed volumes with high resolution and contrast to address biological research questions within feasible acquisition time frames.

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