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Cryo-EM structure of a functional monomeric Photosystem I from Thermosynechococcus elongatus reveals red chlorophyll cluster
A high-resolution structure of trimeric cyanobacterial Photosystem I (PSI) from Thermosynechococcus elongatus was reported as the first atomic model of PSI almost 20 years ago. However, the monomeric PSI structure has not yet been reported despite long-standing interest in its structure and extensiv...
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/PMC7940658/ https://www.ncbi.nlm.nih.gov/pubmed/33686186 http://dx.doi.org/10.1038/s42003-021-01808-9 |
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author | Çoruh, Orkun Frank, Anna Tanaka, Hideaki Kawamoto, Akihiro El-Mohsnawy, Eithar Kato, Takayuki Namba, Keiichi Gerle, Christoph Nowaczyk, Marc M. Kurisu, Genji |
author_facet | Çoruh, Orkun Frank, Anna Tanaka, Hideaki Kawamoto, Akihiro El-Mohsnawy, Eithar Kato, Takayuki Namba, Keiichi Gerle, Christoph Nowaczyk, Marc M. Kurisu, Genji |
author_sort | Çoruh, Orkun |
collection | PubMed |
description | A high-resolution structure of trimeric cyanobacterial Photosystem I (PSI) from Thermosynechococcus elongatus was reported as the first atomic model of PSI almost 20 years ago. However, the monomeric PSI structure has not yet been reported despite long-standing interest in its structure and extensive spectroscopic characterization of the loss of red chlorophylls upon monomerization. Here, we describe the structure of monomeric PSI from Thermosynechococcus elongatus BP-1. Comparison with the trimer structure gave detailed insights into monomerization-induced changes in both the central trimerization domain and the peripheral regions of the complex. Monomerization-induced loss of red chlorophylls is assigned to a cluster of chlorophylls adjacent to PsaX. Based on our findings, we propose a role of PsaX in the stabilization of red chlorophylls and that lipids of the surrounding membrane present a major source of thermal energy for uphill excitation energy transfer from red chlorophylls to P700. |
format | Online Article Text |
id | pubmed-7940658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79406582021-03-28 Cryo-EM structure of a functional monomeric Photosystem I from Thermosynechococcus elongatus reveals red chlorophyll cluster Çoruh, Orkun Frank, Anna Tanaka, Hideaki Kawamoto, Akihiro El-Mohsnawy, Eithar Kato, Takayuki Namba, Keiichi Gerle, Christoph Nowaczyk, Marc M. Kurisu, Genji Commun Biol Article A high-resolution structure of trimeric cyanobacterial Photosystem I (PSI) from Thermosynechococcus elongatus was reported as the first atomic model of PSI almost 20 years ago. However, the monomeric PSI structure has not yet been reported despite long-standing interest in its structure and extensive spectroscopic characterization of the loss of red chlorophylls upon monomerization. Here, we describe the structure of monomeric PSI from Thermosynechococcus elongatus BP-1. Comparison with the trimer structure gave detailed insights into monomerization-induced changes in both the central trimerization domain and the peripheral regions of the complex. Monomerization-induced loss of red chlorophylls is assigned to a cluster of chlorophylls adjacent to PsaX. Based on our findings, we propose a role of PsaX in the stabilization of red chlorophylls and that lipids of the surrounding membrane present a major source of thermal energy for uphill excitation energy transfer from red chlorophylls to P700. Nature Publishing Group UK 2021-03-08 /pmc/articles/PMC7940658/ /pubmed/33686186 http://dx.doi.org/10.1038/s42003-021-01808-9 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 Çoruh, Orkun Frank, Anna Tanaka, Hideaki Kawamoto, Akihiro El-Mohsnawy, Eithar Kato, Takayuki Namba, Keiichi Gerle, Christoph Nowaczyk, Marc M. Kurisu, Genji Cryo-EM structure of a functional monomeric Photosystem I from Thermosynechococcus elongatus reveals red chlorophyll cluster |
title | Cryo-EM structure of a functional monomeric Photosystem I from Thermosynechococcus elongatus reveals red chlorophyll cluster |
title_full | Cryo-EM structure of a functional monomeric Photosystem I from Thermosynechococcus elongatus reveals red chlorophyll cluster |
title_fullStr | Cryo-EM structure of a functional monomeric Photosystem I from Thermosynechococcus elongatus reveals red chlorophyll cluster |
title_full_unstemmed | Cryo-EM structure of a functional monomeric Photosystem I from Thermosynechococcus elongatus reveals red chlorophyll cluster |
title_short | Cryo-EM structure of a functional monomeric Photosystem I from Thermosynechococcus elongatus reveals red chlorophyll cluster |
title_sort | cryo-em structure of a functional monomeric photosystem i from thermosynechococcus elongatus reveals red chlorophyll cluster |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940658/ https://www.ncbi.nlm.nih.gov/pubmed/33686186 http://dx.doi.org/10.1038/s42003-021-01808-9 |
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