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How the Protein Environment Can Tune the Energy, the Coupling, and the Ultrafast Dynamics of Interacting Chlorophylls: The Example of the Water-Soluble Chlorophyll Protein
[Image: see text] The interplay between active molecules and the protein environment in light-harvesting complexes tunes the photophysics and the dynamical properties of pigment–protein complexes in a subtle way, which is not fully understood. Here we characterized the photophysics and the ultrafast...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995254/ https://www.ncbi.nlm.nih.gov/pubmed/31952446 http://dx.doi.org/10.1021/acs.jpclett.9b03628 |
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author | Fresch, Elisa Meneghin, Elena Agostini, Alessandro Paulsen, Harald Carbonera, Donatella Collini, Elisabetta |
author_facet | Fresch, Elisa Meneghin, Elena Agostini, Alessandro Paulsen, Harald Carbonera, Donatella Collini, Elisabetta |
author_sort | Fresch, Elisa |
collection | PubMed |
description | [Image: see text] The interplay between active molecules and the protein environment in light-harvesting complexes tunes the photophysics and the dynamical properties of pigment–protein complexes in a subtle way, which is not fully understood. Here we characterized the photophysics and the ultrafast dynamics of four variants of the water-soluble chlorophyll protein (WSCP) as an ideal model system to study the behavior of strongly interacting chlorophylls. We found that when coordinated by the WSCP protein, the presence of the formyl group in chlorophyll b replacing the methyl group in chlorophyll a strongly affects the exciton energy and the dynamics of the system, opening up the possibility of tuning the photophysics and the transport properties of multichromophores by engineering specific interactions with the surroundings. |
format | Online Article Text |
id | pubmed-7995254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79952542021-03-29 How the Protein Environment Can Tune the Energy, the Coupling, and the Ultrafast Dynamics of Interacting Chlorophylls: The Example of the Water-Soluble Chlorophyll Protein Fresch, Elisa Meneghin, Elena Agostini, Alessandro Paulsen, Harald Carbonera, Donatella Collini, Elisabetta J Phys Chem Lett [Image: see text] The interplay between active molecules and the protein environment in light-harvesting complexes tunes the photophysics and the dynamical properties of pigment–protein complexes in a subtle way, which is not fully understood. Here we characterized the photophysics and the ultrafast dynamics of four variants of the water-soluble chlorophyll protein (WSCP) as an ideal model system to study the behavior of strongly interacting chlorophylls. We found that when coordinated by the WSCP protein, the presence of the formyl group in chlorophyll b replacing the methyl group in chlorophyll a strongly affects the exciton energy and the dynamics of the system, opening up the possibility of tuning the photophysics and the transport properties of multichromophores by engineering specific interactions with the surroundings. American Chemical Society 2020-01-17 2020-02-06 /pmc/articles/PMC7995254/ /pubmed/31952446 http://dx.doi.org/10.1021/acs.jpclett.9b03628 Text en Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Fresch, Elisa Meneghin, Elena Agostini, Alessandro Paulsen, Harald Carbonera, Donatella Collini, Elisabetta How the Protein Environment Can Tune the Energy, the Coupling, and the Ultrafast Dynamics of Interacting Chlorophylls: The Example of the Water-Soluble Chlorophyll Protein |
title | How the Protein Environment Can Tune the Energy, the
Coupling, and the Ultrafast Dynamics of Interacting Chlorophylls:
The Example of the Water-Soluble Chlorophyll Protein |
title_full | How the Protein Environment Can Tune the Energy, the
Coupling, and the Ultrafast Dynamics of Interacting Chlorophylls:
The Example of the Water-Soluble Chlorophyll Protein |
title_fullStr | How the Protein Environment Can Tune the Energy, the
Coupling, and the Ultrafast Dynamics of Interacting Chlorophylls:
The Example of the Water-Soluble Chlorophyll Protein |
title_full_unstemmed | How the Protein Environment Can Tune the Energy, the
Coupling, and the Ultrafast Dynamics of Interacting Chlorophylls:
The Example of the Water-Soluble Chlorophyll Protein |
title_short | How the Protein Environment Can Tune the Energy, the
Coupling, and the Ultrafast Dynamics of Interacting Chlorophylls:
The Example of the Water-Soluble Chlorophyll Protein |
title_sort | how the protein environment can tune the energy, the
coupling, and the ultrafast dynamics of interacting chlorophylls:
the example of the water-soluble chlorophyll protein |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995254/ https://www.ncbi.nlm.nih.gov/pubmed/31952446 http://dx.doi.org/10.1021/acs.jpclett.9b03628 |
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