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  Routine collection of high-resolution cryo-EM datasets using 200 KV transmission electron microscope

Koh, A., Khavnekar, S., Yang, W., Karia, D., Cats, D., van der Ploeg, R., Grollios, F., Raschdorf, O., Kotecha, A., & Nemecek, D. (2022). Routine collection of high-resolution cryo-EM datasets using 200 KV transmission electron microscope. Journal of Visualized Experiments, (181):. doi:10.3791/63519.

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-000A-D23C-6 版のパーマリンク: https://hdl.handle.net/21.11116/0000-000F-F864-9
資料種別: 学術論文

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 作成者:
Koh, Adrian, 著者
Khavnekar, Sagar1, 著者           
Yang, Wen, 著者
Karia, Dimple, 著者
Cats, Dennis, 著者
van der Ploeg, Rob, 著者
Grollios, Fanis, 著者
Raschdorf, Oliver, 著者
Kotecha, Abhay, 著者
Nemecek, Daniel, 著者
所属:
1Baumeister, Wolfgang / Molecular Structural Biology, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565142              

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キーワード: EWALD SPHERE; PROTEINScience & Technology - Other Topics;
 要旨: Cryo-electron microscopy (cryo-EM) has been established as a routine method for protein structure determination during the past decade, taking an ever-increasing share of published structural data. Recent advances in TEM technology and automation have boosted both the speed of data collection and quality of acquired images while simultaneously decreasing the required level of expertise for obtaining cryo-EM maps at sub-3 angstrom resolutions. While most of such high-resolution structures have been obtained using state-of-the-art 300 kV cryo-TEM systems, high-resolution structures can be also obtained with 200 kV cryo-TEM systems, especially when equipped with an energy filter. Additionally, automation of microscope alignments and data collection with real-time image quality assessment reduces system complexity and assures optimal microscope settings, resulting in increased yield of high-quality images and overall throughput of data collection. This protocol demonstrates the implementation of recent technological advances and automation features on a 200 kV cryo-transmission electron microscope and shows how to collect data for the reconstruction of 3D maps that are sufficient for de novo atomic model building. We focus on best practices, critical variables, and common issues that must be considered to enable the routine collection of such high-resolution cryo-EM datasets. Particularly the following essential topics are reviewed in detail: i) automation of microscope alignments, ii) selection of suitable areas for data acquisition, iii) optimal optical parameters for high-quality, high-throughput data collection, iv) energy filter tuning for zero-loss imaging, and v) data management and quality assessment. Application of the best practices and improvement of achievable resolution using an energy filter will be demonstrated on the example of apo-ferritin that was reconstructed to 1.6 angstrom, and Thermoplasma acidophilum 20S proteasome reconstructed to 2.1-angstrom resolution using a 200 kV TEM equipped with an energy filter and a direct electron detector.

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言語: eng - English
 日付: 2022-03-16
 出版の状態: 出版
 ページ: 25
 出版情報: -
 目次: -
 査読: -
 識別子(DOI, ISBNなど): ISI: 000830430700020
DOI: 10.3791/63519
 学位: -

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出版物 1

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出版物名: Journal of Visualized Experiments
  その他 : Journal of Visualized Experiments: JoVE
  省略形 : J. Vis. Exp.
種別: 学術雑誌
 著者・編者:
所属:
出版社, 出版地: Rockville Pike, Bethesda MD : JoVE
ページ: - 巻号: (181) 通巻号: e63519 開始・終了ページ: - 識別子(ISBN, ISSN, DOIなど): ISSN: 1940-087X
CoNE: https://pure.mpg.de/cone/journals/resource/1940087X