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Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution
In electron cryomicroscopy (cryo-EM), molecular images of vitrified biological samples are obtained by conventional transmission microscopy (CTEM) using large underfocuses and subsequently computationally combined into a high-resolution three-dimensional structure. Here, we apply scanning transmissi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467914/ https://www.ncbi.nlm.nih.gov/pubmed/36064775 http://dx.doi.org/10.1038/s41592-022-01586-0 |
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author | Lazić, Ivan Wirix, Maarten Leidl, Max Leo de Haas, Felix Mann, Daniel Beckers, Maximilian Pechnikova, Evgeniya V. Müller-Caspary, Knut Egoavil, Ricardo Bosch, Eric G. T. Sachse, Carsten |
author_facet | Lazić, Ivan Wirix, Maarten Leidl, Max Leo de Haas, Felix Mann, Daniel Beckers, Maximilian Pechnikova, Evgeniya V. Müller-Caspary, Knut Egoavil, Ricardo Bosch, Eric G. T. Sachse, Carsten |
author_sort | Lazić, Ivan |
collection | PubMed |
description | In electron cryomicroscopy (cryo-EM), molecular images of vitrified biological samples are obtained by conventional transmission microscopy (CTEM) using large underfocuses and subsequently computationally combined into a high-resolution three-dimensional structure. Here, we apply scanning transmission electron microscopy (STEM) using the integrated differential phase contrast mode also known as iDPC–STEM to two cryo-EM test specimens, keyhole limpet hemocyanin (KLH) and tobacco mosaic virus (TMV). The micrographs show complete contrast transfer to high resolution and enable the cryo-EM structure determination for KLH at 6.5 Å resolution, as well as for TMV at 3.5 Å resolution using single-particle reconstruction methods, which share identical features with maps obtained by CTEM of a previously acquired same-sized TMV data set. These data show that STEM imaging in general, and in particular the iDPC–STEM approach, can be applied to vitrified single-particle specimens to determine near-atomic resolution cryo-EM structures of biological macromolecules. |
format | Online Article Text |
id | pubmed-9467914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-94679142022-09-14 Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution Lazić, Ivan Wirix, Maarten Leidl, Max Leo de Haas, Felix Mann, Daniel Beckers, Maximilian Pechnikova, Evgeniya V. Müller-Caspary, Knut Egoavil, Ricardo Bosch, Eric G. T. Sachse, Carsten Nat Methods Article In electron cryomicroscopy (cryo-EM), molecular images of vitrified biological samples are obtained by conventional transmission microscopy (CTEM) using large underfocuses and subsequently computationally combined into a high-resolution three-dimensional structure. Here, we apply scanning transmission electron microscopy (STEM) using the integrated differential phase contrast mode also known as iDPC–STEM to two cryo-EM test specimens, keyhole limpet hemocyanin (KLH) and tobacco mosaic virus (TMV). The micrographs show complete contrast transfer to high resolution and enable the cryo-EM structure determination for KLH at 6.5 Å resolution, as well as for TMV at 3.5 Å resolution using single-particle reconstruction methods, which share identical features with maps obtained by CTEM of a previously acquired same-sized TMV data set. These data show that STEM imaging in general, and in particular the iDPC–STEM approach, can be applied to vitrified single-particle specimens to determine near-atomic resolution cryo-EM structures of biological macromolecules. Nature Publishing Group US 2022-09-05 2022 /pmc/articles/PMC9467914/ /pubmed/36064775 http://dx.doi.org/10.1038/s41592-022-01586-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lazić, Ivan Wirix, Maarten Leidl, Max Leo de Haas, Felix Mann, Daniel Beckers, Maximilian Pechnikova, Evgeniya V. Müller-Caspary, Knut Egoavil, Ricardo Bosch, Eric G. T. Sachse, Carsten Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution |
title | Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution |
title_full | Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution |
title_fullStr | Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution |
title_full_unstemmed | Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution |
title_short | Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution |
title_sort | single-particle cryo-em structures from idpc–stem at near-atomic resolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9467914/ https://www.ncbi.nlm.nih.gov/pubmed/36064775 http://dx.doi.org/10.1038/s41592-022-01586-0 |
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