Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Ziyu, Vercellino, Irene, Knoppová, Jana, Sobotka, Roman, Murray, James W., Nixon, Peter J., Sazanov, Leonid A., Komenda, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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
_version_ 1785085099158536192
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
work_keys_str_mv AT zhaoziyu theycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT vercellinoirene theycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT knoppovajana theycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT sobotkaroman theycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT murrayjamesw theycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT nixonpeterj theycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT sazanovleonida theycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT komendajosef theycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT zhaoziyu ycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT vercellinoirene ycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT knoppovajana ycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT sobotkaroman ycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT murrayjamesw ycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT nixonpeterj ycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT sazanovleonida ycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis
AT komendajosef ycf48accessoryfactoroccupiesthesiteoftheoxygenevolvingmanganeseclusterduringphotosystemiibiogenesis