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The molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling

The light-harvesting in photosynthetic purple bacteria can be tuned in response to the light conditions during cell growth. One of the used strategies is to change the energy of the excitons in the major fight-harvesting complex, commonly known as LH2. In the present study we report the first system...

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Autores principales: Cardoso Ramos, Felipe, Nottoli, Michele, Cupellini, Lorenzo, Mennucci, Benedetta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988754/
https://www.ncbi.nlm.nih.gov/pubmed/32055335
http://dx.doi.org/10.1039/c9sc02886b
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author Cardoso Ramos, Felipe
Nottoli, Michele
Cupellini, Lorenzo
Mennucci, Benedetta
author_facet Cardoso Ramos, Felipe
Nottoli, Michele
Cupellini, Lorenzo
Mennucci, Benedetta
author_sort Cardoso Ramos, Felipe
collection PubMed
description The light-harvesting in photosynthetic purple bacteria can be tuned in response to the light conditions during cell growth. One of the used strategies is to change the energy of the excitons in the major fight-harvesting complex, commonly known as LH2. In the present study we report the first systematic investigation of the microscopic origin of the exciton tuning using three complexes, namely the common (high-light) and the low-light forms of LH2 from Rps. acidophila plus a third complex analogous to the PucD complex from Rps. palustris. The study is based on the combination of classical molecular dynamics of each complex in a lipid membrane and excitonic calculations based on a multiscale quantum mechanics/molecular mechanics approach including a polarizable embedding. From the comparative analysis, it comes out that the mechanisms that govern the adaptation of the complex to different light conditions use the different H-bonding environment around the bacteriochlorophyll pigments to dynamically control both internal and inter-pigment degrees of freedom. While the former have a large effect on the site energies, the latter significantly change the electronic couplings, but only the combination of the two effects can fully reproduce the tuning of the final excitons and explain the observed spectroscopic differences.
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spelling pubmed-69887542020-02-13 The molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling Cardoso Ramos, Felipe Nottoli, Michele Cupellini, Lorenzo Mennucci, Benedetta Chem Sci Chemistry The light-harvesting in photosynthetic purple bacteria can be tuned in response to the light conditions during cell growth. One of the used strategies is to change the energy of the excitons in the major fight-harvesting complex, commonly known as LH2. In the present study we report the first systematic investigation of the microscopic origin of the exciton tuning using three complexes, namely the common (high-light) and the low-light forms of LH2 from Rps. acidophila plus a third complex analogous to the PucD complex from Rps. palustris. The study is based on the combination of classical molecular dynamics of each complex in a lipid membrane and excitonic calculations based on a multiscale quantum mechanics/molecular mechanics approach including a polarizable embedding. From the comparative analysis, it comes out that the mechanisms that govern the adaptation of the complex to different light conditions use the different H-bonding environment around the bacteriochlorophyll pigments to dynamically control both internal and inter-pigment degrees of freedom. While the former have a large effect on the site energies, the latter significantly change the electronic couplings, but only the combination of the two effects can fully reproduce the tuning of the final excitons and explain the observed spectroscopic differences. Royal Society of Chemistry 2019-09-27 /pmc/articles/PMC6988754/ /pubmed/32055335 http://dx.doi.org/10.1039/c9sc02886b Text en This journal is © The Royal Society of Chemistry 2019 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Cardoso Ramos, Felipe
Nottoli, Michele
Cupellini, Lorenzo
Mennucci, Benedetta
The molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling
title The molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling
title_full The molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling
title_fullStr The molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling
title_full_unstemmed The molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling
title_short The molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling
title_sort molecular mechanisms of light adaption in light-harvesting complexes of purple bacteria revealed by a multiscale modeling
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988754/
https://www.ncbi.nlm.nih.gov/pubmed/32055335
http://dx.doi.org/10.1039/c9sc02886b
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