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High-resolution cryo-EM structure of photosystem II reveals damage from high-dose electron beams
Photosystem II (PSII) plays a key role in water-splitting and oxygen evolution. X-ray crystallography has revealed its atomic structure and some intermediate structures. However, these structures are in the crystalline state and its final state structure has not been solved. Here we analyzed the str...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985191/ https://www.ncbi.nlm.nih.gov/pubmed/33753866 http://dx.doi.org/10.1038/s42003-021-01919-3 |
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author | Kato, Koji Miyazaki, Naoyuki Hamaguchi, Tasuku Nakajima, Yoshiki Akita, Fusamichi Yonekura, Koji Shen, Jian-Ren |
author_facet | Kato, Koji Miyazaki, Naoyuki Hamaguchi, Tasuku Nakajima, Yoshiki Akita, Fusamichi Yonekura, Koji Shen, Jian-Ren |
author_sort | Kato, Koji |
collection | PubMed |
description | Photosystem II (PSII) plays a key role in water-splitting and oxygen evolution. X-ray crystallography has revealed its atomic structure and some intermediate structures. However, these structures are in the crystalline state and its final state structure has not been solved. Here we analyzed the structure of PSII in solution at 1.95 Å resolution by single-particle cryo-electron microscopy (cryo-EM). The structure obtained is similar to the crystal structure, but a PsbY subunit was visible in the cryo-EM structure, indicating that it represents its physiological state more closely. Electron beam damage was observed at a high-dose in the regions that were easily affected by redox states, and reducing the beam dosage by reducing frames from 50 to 2 yielded a similar resolution but reduced the damage remarkably. This study will serve as a good indicator for determining damage-free cryo-EM structures of not only PSII but also all biological samples, especially redox-active metalloproteins. |
format | Online Article Text |
id | pubmed-7985191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79851912021-04-12 High-resolution cryo-EM structure of photosystem II reveals damage from high-dose electron beams Kato, Koji Miyazaki, Naoyuki Hamaguchi, Tasuku Nakajima, Yoshiki Akita, Fusamichi Yonekura, Koji Shen, Jian-Ren Commun Biol Article Photosystem II (PSII) plays a key role in water-splitting and oxygen evolution. X-ray crystallography has revealed its atomic structure and some intermediate structures. However, these structures are in the crystalline state and its final state structure has not been solved. Here we analyzed the structure of PSII in solution at 1.95 Å resolution by single-particle cryo-electron microscopy (cryo-EM). The structure obtained is similar to the crystal structure, but a PsbY subunit was visible in the cryo-EM structure, indicating that it represents its physiological state more closely. Electron beam damage was observed at a high-dose in the regions that were easily affected by redox states, and reducing the beam dosage by reducing frames from 50 to 2 yielded a similar resolution but reduced the damage remarkably. This study will serve as a good indicator for determining damage-free cryo-EM structures of not only PSII but also all biological samples, especially redox-active metalloproteins. Nature Publishing Group UK 2021-03-22 /pmc/articles/PMC7985191/ /pubmed/33753866 http://dx.doi.org/10.1038/s42003-021-01919-3 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Kato, Koji Miyazaki, Naoyuki Hamaguchi, Tasuku Nakajima, Yoshiki Akita, Fusamichi Yonekura, Koji Shen, Jian-Ren High-resolution cryo-EM structure of photosystem II reveals damage from high-dose electron beams |
title | High-resolution cryo-EM structure of photosystem II reveals damage from high-dose electron beams |
title_full | High-resolution cryo-EM structure of photosystem II reveals damage from high-dose electron beams |
title_fullStr | High-resolution cryo-EM structure of photosystem II reveals damage from high-dose electron beams |
title_full_unstemmed | High-resolution cryo-EM structure of photosystem II reveals damage from high-dose electron beams |
title_short | High-resolution cryo-EM structure of photosystem II reveals damage from high-dose electron beams |
title_sort | high-resolution cryo-em structure of photosystem ii reveals damage from high-dose electron beams |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985191/ https://www.ncbi.nlm.nih.gov/pubmed/33753866 http://dx.doi.org/10.1038/s42003-021-01919-3 |
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