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Combining high throughput and high quality for cryo-electron microscopy data collection

Cryo-electron microscopy (cryo-EM) can be used to elucidate the 3D structure of macromolecular complexes. Driven by technological breakthroughs in electron-microscope and electron-detector development, coupled with improved image-processing procedures, it is now possible to reach high resolution bot...

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Detalles Bibliográficos
Autores principales: Weis, Felix, Hagen, Wim J. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397495/
https://www.ncbi.nlm.nih.gov/pubmed/32744254
http://dx.doi.org/10.1107/S2059798320008347
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author Weis, Felix
Hagen, Wim J. H.
author_facet Weis, Felix
Hagen, Wim J. H.
author_sort Weis, Felix
collection PubMed
description Cryo-electron microscopy (cryo-EM) can be used to elucidate the 3D structure of macromolecular complexes. Driven by technological breakthroughs in electron-microscope and electron-detector development, coupled with improved image-processing procedures, it is now possible to reach high resolution both in single-particle analysis and in cryo-electron tomography and subtomogram-averaging approaches. As a consequence, the way in which cryo-EM data are collected has changed and new challenges have arisen in terms of microscope alignment, aberration correction and imaging parameters. This review describes how high-end data collection is performed at the EMBL Heidelberg cryo-EM platform, presenting recent microscope implementations that allow an increase in throughput while maintaining aberration-free imaging and the optimization of acquisition parameters to collect high-resolution data.
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spelling pubmed-73974952020-08-11 Combining high throughput and high quality for cryo-electron microscopy data collection Weis, Felix Hagen, Wim J. H. Acta Crystallogr D Struct Biol Ccp-EM Cryo-electron microscopy (cryo-EM) can be used to elucidate the 3D structure of macromolecular complexes. Driven by technological breakthroughs in electron-microscope and electron-detector development, coupled with improved image-processing procedures, it is now possible to reach high resolution both in single-particle analysis and in cryo-electron tomography and subtomogram-averaging approaches. As a consequence, the way in which cryo-EM data are collected has changed and new challenges have arisen in terms of microscope alignment, aberration correction and imaging parameters. This review describes how high-end data collection is performed at the EMBL Heidelberg cryo-EM platform, presenting recent microscope implementations that allow an increase in throughput while maintaining aberration-free imaging and the optimization of acquisition parameters to collect high-resolution data. International Union of Crystallography 2020-07-27 /pmc/articles/PMC7397495/ /pubmed/32744254 http://dx.doi.org/10.1107/S2059798320008347 Text en © Weis & Hagen 2020 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/
spellingShingle Ccp-EM
Weis, Felix
Hagen, Wim J. H.
Combining high throughput and high quality for cryo-electron microscopy data collection
title Combining high throughput and high quality for cryo-electron microscopy data collection
title_full Combining high throughput and high quality for cryo-electron microscopy data collection
title_fullStr Combining high throughput and high quality for cryo-electron microscopy data collection
title_full_unstemmed Combining high throughput and high quality for cryo-electron microscopy data collection
title_short Combining high throughput and high quality for cryo-electron microscopy data collection
title_sort combining high throughput and high quality for cryo-electron microscopy data collection
topic Ccp-EM
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397495/
https://www.ncbi.nlm.nih.gov/pubmed/32744254
http://dx.doi.org/10.1107/S2059798320008347
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