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UVC inactivation of pathogenic samples suitable for cryo-EM analysis
Cryo-electron microscopy has become an essential tool to understand structure and function of biological samples. Especially for pathogens, such as disease-causing bacteria and viruses, insights gained by cryo-EM can aid in developing cures. However, due to the biosafety restrictions of pathogens, s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752862/ https://www.ncbi.nlm.nih.gov/pubmed/35017666 http://dx.doi.org/10.1038/s42003-021-02962-w |
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author | Depelteau, Jamie S. Renault, Ludovic Althof, Nynke Cassidy, C. Keith Mendonça, Luiza M. Jensen, Grant J. Resch, Guenter P. Briegel, Ariane |
author_facet | Depelteau, Jamie S. Renault, Ludovic Althof, Nynke Cassidy, C. Keith Mendonça, Luiza M. Jensen, Grant J. Resch, Guenter P. Briegel, Ariane |
author_sort | Depelteau, Jamie S. |
collection | PubMed |
description | Cryo-electron microscopy has become an essential tool to understand structure and function of biological samples. Especially for pathogens, such as disease-causing bacteria and viruses, insights gained by cryo-EM can aid in developing cures. However, due to the biosafety restrictions of pathogens, samples are often treated by chemical fixation to render the pathogen inert, affecting the ultrastructure of the sample. Alternatively, researchers use in vitro or ex vivo models, which are non-pathogenic but lack the complexity of the pathogen of interest. Here we show that ultraviolet-C (UVC) radiation applied at cryogenic temperatures can be used to eliminate or dramatically reduce the infectivity of Vibrio cholerae and the bacterial virus, the ICP1 bacteriophage. We show no discernable structural impact of this treatment of either sample using two cryo-EM methods: cryo-electron tomography followed by sub-tomogram averaging, and single particle analysis (SPA). Additionally, we applied the UVC irradiation to the protein apoferritin (ApoF), which is a widely used test sample for high-resolution SPA studies. The UVC-treated ApoF sample resulted in a 2.1 Å structure indistinguishable from an untreated published map. This research demonstrates that UVC treatment is an effective and inexpensive addition to the cryo-EM sample preparation toolbox. |
format | Online Article Text |
id | pubmed-8752862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87528622022-01-20 UVC inactivation of pathogenic samples suitable for cryo-EM analysis Depelteau, Jamie S. Renault, Ludovic Althof, Nynke Cassidy, C. Keith Mendonça, Luiza M. Jensen, Grant J. Resch, Guenter P. Briegel, Ariane Commun Biol Article Cryo-electron microscopy has become an essential tool to understand structure and function of biological samples. Especially for pathogens, such as disease-causing bacteria and viruses, insights gained by cryo-EM can aid in developing cures. However, due to the biosafety restrictions of pathogens, samples are often treated by chemical fixation to render the pathogen inert, affecting the ultrastructure of the sample. Alternatively, researchers use in vitro or ex vivo models, which are non-pathogenic but lack the complexity of the pathogen of interest. Here we show that ultraviolet-C (UVC) radiation applied at cryogenic temperatures can be used to eliminate or dramatically reduce the infectivity of Vibrio cholerae and the bacterial virus, the ICP1 bacteriophage. We show no discernable structural impact of this treatment of either sample using two cryo-EM methods: cryo-electron tomography followed by sub-tomogram averaging, and single particle analysis (SPA). Additionally, we applied the UVC irradiation to the protein apoferritin (ApoF), which is a widely used test sample for high-resolution SPA studies. The UVC-treated ApoF sample resulted in a 2.1 Å structure indistinguishable from an untreated published map. This research demonstrates that UVC treatment is an effective and inexpensive addition to the cryo-EM sample preparation toolbox. Nature Publishing Group UK 2022-01-11 /pmc/articles/PMC8752862/ /pubmed/35017666 http://dx.doi.org/10.1038/s42003-021-02962-w 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 Depelteau, Jamie S. Renault, Ludovic Althof, Nynke Cassidy, C. Keith Mendonça, Luiza M. Jensen, Grant J. Resch, Guenter P. Briegel, Ariane UVC inactivation of pathogenic samples suitable for cryo-EM analysis |
title | UVC inactivation of pathogenic samples suitable for cryo-EM analysis |
title_full | UVC inactivation of pathogenic samples suitable for cryo-EM analysis |
title_fullStr | UVC inactivation of pathogenic samples suitable for cryo-EM analysis |
title_full_unstemmed | UVC inactivation of pathogenic samples suitable for cryo-EM analysis |
title_short | UVC inactivation of pathogenic samples suitable for cryo-EM analysis |
title_sort | uvc inactivation of pathogenic samples suitable for cryo-em analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752862/ https://www.ncbi.nlm.nih.gov/pubmed/35017666 http://dx.doi.org/10.1038/s42003-021-02962-w |
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