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Large-scale FRET simulations reveal the control parameters of phycobilisome light-harvesting complexes

Phycobilisomes (PBS) are massive structures that absorb and transfer light energy to photochemical reaction centres. Among the range of light harvesting systems, PBS are considered to be excellent solutions for absorption cross-sections but relatively inefficient energy transferring systems. This is...

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Autores principales: Dodson, Emma Joy, Werren, Nicholas, Paltiel, Yossi, Gauger, Erik M., Keren, Nir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709516/
https://www.ncbi.nlm.nih.gov/pubmed/36448289
http://dx.doi.org/10.1098/rsif.2022.0580
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author Dodson, Emma Joy
Werren, Nicholas
Paltiel, Yossi
Gauger, Erik M.
Keren, Nir
author_facet Dodson, Emma Joy
Werren, Nicholas
Paltiel, Yossi
Gauger, Erik M.
Keren, Nir
author_sort Dodson, Emma Joy
collection PubMed
description Phycobilisomes (PBS) are massive structures that absorb and transfer light energy to photochemical reaction centres. Among the range of light harvesting systems, PBS are considered to be excellent solutions for absorption cross-sections but relatively inefficient energy transferring systems. This is due to the combination of a large number of chromophores with intermediate coupling distances. Nevertheless, PBS systems persisted from the origin of oxygenic photosynthesis to present-day cyanobacteria and red algae, organisms that account for approximately half of the primary productivity in the ocean. In this study, we modelled energy transfer through subsets of PBS structures, using a comprehensive dynamic Hamiltonian model. Our approach was applied, initially, to pairs of phycobilin hexamers and then extended to short rods. By manipulating the distances and angles between the structures, we could probe the dynamics of exciton transfer. These simulations suggest that the PBS chromophore network enhances energy distribution over the entire PBS structure—both horizontally and vertically to the rod axis. Furthermore, energy transfer was found to be relatively immune to the effects of distances or rotations, within the range of intermediate coupling distances. Therefore, we suggest that the PBS provides unique advantages and flexibility to aquatic photosynthesis.
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spelling pubmed-97095162023-02-15 Large-scale FRET simulations reveal the control parameters of phycobilisome light-harvesting complexes Dodson, Emma Joy Werren, Nicholas Paltiel, Yossi Gauger, Erik M. Keren, Nir J R Soc Interface Life Sciences–Chemistry interface Phycobilisomes (PBS) are massive structures that absorb and transfer light energy to photochemical reaction centres. Among the range of light harvesting systems, PBS are considered to be excellent solutions for absorption cross-sections but relatively inefficient energy transferring systems. This is due to the combination of a large number of chromophores with intermediate coupling distances. Nevertheless, PBS systems persisted from the origin of oxygenic photosynthesis to present-day cyanobacteria and red algae, organisms that account for approximately half of the primary productivity in the ocean. In this study, we modelled energy transfer through subsets of PBS structures, using a comprehensive dynamic Hamiltonian model. Our approach was applied, initially, to pairs of phycobilin hexamers and then extended to short rods. By manipulating the distances and angles between the structures, we could probe the dynamics of exciton transfer. These simulations suggest that the PBS chromophore network enhances energy distribution over the entire PBS structure—both horizontally and vertically to the rod axis. Furthermore, energy transfer was found to be relatively immune to the effects of distances or rotations, within the range of intermediate coupling distances. Therefore, we suggest that the PBS provides unique advantages and flexibility to aquatic photosynthesis. The Royal Society 2022-11-30 /pmc/articles/PMC9709516/ /pubmed/36448289 http://dx.doi.org/10.1098/rsif.2022.0580 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Chemistry interface
Dodson, Emma Joy
Werren, Nicholas
Paltiel, Yossi
Gauger, Erik M.
Keren, Nir
Large-scale FRET simulations reveal the control parameters of phycobilisome light-harvesting complexes
title Large-scale FRET simulations reveal the control parameters of phycobilisome light-harvesting complexes
title_full Large-scale FRET simulations reveal the control parameters of phycobilisome light-harvesting complexes
title_fullStr Large-scale FRET simulations reveal the control parameters of phycobilisome light-harvesting complexes
title_full_unstemmed Large-scale FRET simulations reveal the control parameters of phycobilisome light-harvesting complexes
title_short Large-scale FRET simulations reveal the control parameters of phycobilisome light-harvesting complexes
title_sort large-scale fret simulations reveal the control parameters of phycobilisome light-harvesting complexes
topic Life Sciences–Chemistry interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709516/
https://www.ncbi.nlm.nih.gov/pubmed/36448289
http://dx.doi.org/10.1098/rsif.2022.0580
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