Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fresch, Elisa, Meneghin, Elena, Agostini, Alessandro, Paulsen, Harald, Carbonera, Donatella, Collini, Elisabetta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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
_version_ 1783669884464398336
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
work_keys_str_mv AT freschelisa howtheproteinenvironmentcantunetheenergythecouplingandtheultrafastdynamicsofinteractingchlorophyllstheexampleofthewatersolublechlorophyllprotein
AT meneghinelena howtheproteinenvironmentcantunetheenergythecouplingandtheultrafastdynamicsofinteractingchlorophyllstheexampleofthewatersolublechlorophyllprotein
AT agostinialessandro howtheproteinenvironmentcantunetheenergythecouplingandtheultrafastdynamicsofinteractingchlorophyllstheexampleofthewatersolublechlorophyllprotein
AT paulsenharald howtheproteinenvironmentcantunetheenergythecouplingandtheultrafastdynamicsofinteractingchlorophyllstheexampleofthewatersolublechlorophyllprotein
AT carboneradonatella howtheproteinenvironmentcantunetheenergythecouplingandtheultrafastdynamicsofinteractingchlorophyllstheexampleofthewatersolublechlorophyllprotein
AT collinielisabetta howtheproteinenvironmentcantunetheenergythecouplingandtheultrafastdynamicsofinteractingchlorophyllstheexampleofthewatersolublechlorophyllprotein