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The Ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem II biogenesis
Robust oxygenic photosynthesis requires a suite of accessory factors to ensure efficient assembly and repair of the oxygen-evolving photosystem two (PSII) complex. The highly conserved Ycf48 assembly factor binds to the newly synthesized D1 reaction center polypeptide and promotes the initial steps...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403576/ https://www.ncbi.nlm.nih.gov/pubmed/37542031 http://dx.doi.org/10.1038/s41467-023-40388-6 |
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author | Zhao, Ziyu Vercellino, Irene Knoppová, Jana Sobotka, Roman Murray, James W. Nixon, Peter J. Sazanov, Leonid A. Komenda, Josef |
author_facet | Zhao, Ziyu Vercellino, Irene Knoppová, Jana Sobotka, Roman Murray, James W. Nixon, Peter J. Sazanov, Leonid A. Komenda, Josef |
author_sort | Zhao, Ziyu |
collection | PubMed |
description | Robust oxygenic photosynthesis requires a suite of accessory factors to ensure efficient assembly and repair of the oxygen-evolving photosystem two (PSII) complex. The highly conserved Ycf48 assembly factor binds to the newly synthesized D1 reaction center polypeptide and promotes the initial steps of PSII assembly, but its binding site is unclear. Here we use cryo-electron microscopy to determine the structure of a cyanobacterial PSII D1/D2 reaction center assembly complex with Ycf48 attached. Ycf48, a 7-bladed beta propeller, binds to the amino-acid residues of D1 that ultimately ligate the water-oxidising Mn(4)CaO(5) cluster, thereby preventing the premature binding of Mn(2+) and Ca(2+) ions and protecting the site from damage. Interactions with D2 help explain how Ycf48 promotes assembly of the D1/D2 complex. Overall, our work provides valuable insights into the early stages of PSII assembly and the structural changes that create the binding site for the Mn(4)CaO(5) cluster. |
format | Online Article Text |
id | pubmed-10403576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104035762023-08-06 The Ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem II biogenesis Zhao, Ziyu Vercellino, Irene Knoppová, Jana Sobotka, Roman Murray, James W. Nixon, Peter J. Sazanov, Leonid A. Komenda, Josef Nat Commun Article Robust oxygenic photosynthesis requires a suite of accessory factors to ensure efficient assembly and repair of the oxygen-evolving photosystem two (PSII) complex. The highly conserved Ycf48 assembly factor binds to the newly synthesized D1 reaction center polypeptide and promotes the initial steps of PSII assembly, but its binding site is unclear. Here we use cryo-electron microscopy to determine the structure of a cyanobacterial PSII D1/D2 reaction center assembly complex with Ycf48 attached. Ycf48, a 7-bladed beta propeller, binds to the amino-acid residues of D1 that ultimately ligate the water-oxidising Mn(4)CaO(5) cluster, thereby preventing the premature binding of Mn(2+) and Ca(2+) ions and protecting the site from damage. Interactions with D2 help explain how Ycf48 promotes assembly of the D1/D2 complex. Overall, our work provides valuable insights into the early stages of PSII assembly and the structural changes that create the binding site for the Mn(4)CaO(5) cluster. Nature Publishing Group UK 2023-08-04 /pmc/articles/PMC10403576/ /pubmed/37542031 http://dx.doi.org/10.1038/s41467-023-40388-6 Text en © The Author(s) 2023 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 Zhao, Ziyu Vercellino, Irene Knoppová, Jana Sobotka, Roman Murray, James W. Nixon, Peter J. Sazanov, Leonid A. Komenda, Josef The Ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem II biogenesis |
title | The Ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem II biogenesis |
title_full | The Ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem II biogenesis |
title_fullStr | The Ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem II biogenesis |
title_full_unstemmed | The Ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem II biogenesis |
title_short | The Ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem II biogenesis |
title_sort | ycf48 accessory factor occupies the site of the oxygen-evolving manganese cluster during photosystem ii biogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403576/ https://www.ncbi.nlm.nih.gov/pubmed/37542031 http://dx.doi.org/10.1038/s41467-023-40388-6 |
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