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Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy

Photochemical reaction centers are the engines that drive photosynthesis. The reaction center from heliobacteria (HbRC) has been proposed to most closely resemble the common ancestor of photosynthetic reaction centers, motivating a detailed understanding of its structure-function relationship. The r...

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Autores principales: Song, Yin, Sechrist, Riley, Nguyen, Hoang H., Johnson, William, Abramavicius, Darius, Redding, Kevin E., Ogilvie, Jennifer P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121816/
https://www.ncbi.nlm.nih.gov/pubmed/33990569
http://dx.doi.org/10.1038/s41467-021-23060-9
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author Song, Yin
Sechrist, Riley
Nguyen, Hoang H.
Johnson, William
Abramavicius, Darius
Redding, Kevin E.
Ogilvie, Jennifer P.
author_facet Song, Yin
Sechrist, Riley
Nguyen, Hoang H.
Johnson, William
Abramavicius, Darius
Redding, Kevin E.
Ogilvie, Jennifer P.
author_sort Song, Yin
collection PubMed
description Photochemical reaction centers are the engines that drive photosynthesis. The reaction center from heliobacteria (HbRC) has been proposed to most closely resemble the common ancestor of photosynthetic reaction centers, motivating a detailed understanding of its structure-function relationship. The recent elucidation of the HbRC crystal structure motivates advanced spectroscopic studies of its excitonic structure and charge separation mechanism. We perform multispectral two-dimensional electronic spectroscopy of the HbRC and corresponding numerical simulations, resolving the electronic structure and testing and refining recent excitonic models. Through extensive examination of the kinetic data by lifetime density analysis and global target analysis, we reveal that charge separation proceeds via a single pathway in which the distinct A(0) chlorophyll a pigment is the primary electron acceptor. In addition, we find strong delocalization of the charge separation intermediate. Our findings have general implications for the understanding of photosynthetic charge separation mechanisms, and how they might be tuned to achieve different functional goals.
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spelling pubmed-81218162021-05-18 Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy Song, Yin Sechrist, Riley Nguyen, Hoang H. Johnson, William Abramavicius, Darius Redding, Kevin E. Ogilvie, Jennifer P. Nat Commun Article Photochemical reaction centers are the engines that drive photosynthesis. The reaction center from heliobacteria (HbRC) has been proposed to most closely resemble the common ancestor of photosynthetic reaction centers, motivating a detailed understanding of its structure-function relationship. The recent elucidation of the HbRC crystal structure motivates advanced spectroscopic studies of its excitonic structure and charge separation mechanism. We perform multispectral two-dimensional electronic spectroscopy of the HbRC and corresponding numerical simulations, resolving the electronic structure and testing and refining recent excitonic models. Through extensive examination of the kinetic data by lifetime density analysis and global target analysis, we reveal that charge separation proceeds via a single pathway in which the distinct A(0) chlorophyll a pigment is the primary electron acceptor. In addition, we find strong delocalization of the charge separation intermediate. Our findings have general implications for the understanding of photosynthetic charge separation mechanisms, and how they might be tuned to achieve different functional goals. Nature Publishing Group UK 2021-05-14 /pmc/articles/PMC8121816/ /pubmed/33990569 http://dx.doi.org/10.1038/s41467-021-23060-9 Text en © The Author(s) 2021 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
Song, Yin
Sechrist, Riley
Nguyen, Hoang H.
Johnson, William
Abramavicius, Darius
Redding, Kevin E.
Ogilvie, Jennifer P.
Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy
title Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy
title_full Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy
title_fullStr Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy
title_full_unstemmed Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy
title_short Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy
title_sort excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8121816/
https://www.ncbi.nlm.nih.gov/pubmed/33990569
http://dx.doi.org/10.1038/s41467-021-23060-9
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