Cargando…

Fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants

Photosynthetic antenna proteins can be thought of as “programmed solvents”, which bind pigments at specific mutual orientations, thus tuning the overall energetic landscape and ensuring highly efficient light-harvesting. While positioning of chlorophyll cofactors is well understood and rationalized...

Descripción completa

Detalles Bibliográficos
Autores principales: Balevičius, Vytautas, Fox, Kieran F., Bricker, William P., Jurinovich, Sandro, Prandi, Ingrid G., Mennucci, Benedetta, Duffy, Christopher D. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655323/
https://www.ncbi.nlm.nih.gov/pubmed/29066753
http://dx.doi.org/10.1038/s41598-017-13720-6
_version_ 1783273514432724992
author Balevičius, Vytautas
Fox, Kieran F.
Bricker, William P.
Jurinovich, Sandro
Prandi, Ingrid G.
Mennucci, Benedetta
Duffy, Christopher D. P.
author_facet Balevičius, Vytautas
Fox, Kieran F.
Bricker, William P.
Jurinovich, Sandro
Prandi, Ingrid G.
Mennucci, Benedetta
Duffy, Christopher D. P.
author_sort Balevičius, Vytautas
collection PubMed
description Photosynthetic antenna proteins can be thought of as “programmed solvents”, which bind pigments at specific mutual orientations, thus tuning the overall energetic landscape and ensuring highly efficient light-harvesting. While positioning of chlorophyll cofactors is well understood and rationalized by the principle of an “energy funnel”, the carotenoids still pose many open questions. Particularly, their short excited state lifetime (<25 ps) renders them potential energy sinks able to compete with the reaction centers and drastically undermine light-harvesting efficiency. Exploration of the orientational phase-space revealed that the placement of central carotenoids minimizes their interaction with the nearest chlorophylls in the plant antenna complexes LHCII, CP26, CP29 and LHCI. At the same time we show that this interaction is highly sensitive to structural perturbations, which has a profound effect on the overall lifetime of the complex. This links the protein dynamics to the light-harvesting regulation in plants by the carotenoids.
format Online
Article
Text
id pubmed-5655323
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-56553232017-10-31 Fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants Balevičius, Vytautas Fox, Kieran F. Bricker, William P. Jurinovich, Sandro Prandi, Ingrid G. Mennucci, Benedetta Duffy, Christopher D. P. Sci Rep Article Photosynthetic antenna proteins can be thought of as “programmed solvents”, which bind pigments at specific mutual orientations, thus tuning the overall energetic landscape and ensuring highly efficient light-harvesting. While positioning of chlorophyll cofactors is well understood and rationalized by the principle of an “energy funnel”, the carotenoids still pose many open questions. Particularly, their short excited state lifetime (<25 ps) renders them potential energy sinks able to compete with the reaction centers and drastically undermine light-harvesting efficiency. Exploration of the orientational phase-space revealed that the placement of central carotenoids minimizes their interaction with the nearest chlorophylls in the plant antenna complexes LHCII, CP26, CP29 and LHCI. At the same time we show that this interaction is highly sensitive to structural perturbations, which has a profound effect on the overall lifetime of the complex. This links the protein dynamics to the light-harvesting regulation in plants by the carotenoids. Nature Publishing Group UK 2017-10-24 /pmc/articles/PMC5655323/ /pubmed/29066753 http://dx.doi.org/10.1038/s41598-017-13720-6 Text en © The Author(s) 2017 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/.
spellingShingle Article
Balevičius, Vytautas
Fox, Kieran F.
Bricker, William P.
Jurinovich, Sandro
Prandi, Ingrid G.
Mennucci, Benedetta
Duffy, Christopher D. P.
Fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants
title Fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants
title_full Fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants
title_fullStr Fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants
title_full_unstemmed Fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants
title_short Fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants
title_sort fine control of chlorophyll-carotenoid interactions defines the functionality of light-harvesting proteins in plants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655323/
https://www.ncbi.nlm.nih.gov/pubmed/29066753
http://dx.doi.org/10.1038/s41598-017-13720-6
work_keys_str_mv AT baleviciusvytautas finecontrolofchlorophyllcarotenoidinteractionsdefinesthefunctionalityoflightharvestingproteinsinplants
AT foxkieranf finecontrolofchlorophyllcarotenoidinteractionsdefinesthefunctionalityoflightharvestingproteinsinplants
AT brickerwilliamp finecontrolofchlorophyllcarotenoidinteractionsdefinesthefunctionalityoflightharvestingproteinsinplants
AT jurinovichsandro finecontrolofchlorophyllcarotenoidinteractionsdefinesthefunctionalityoflightharvestingproteinsinplants
AT prandiingridg finecontrolofchlorophyllcarotenoidinteractionsdefinesthefunctionalityoflightharvestingproteinsinplants
AT mennuccibenedetta finecontrolofchlorophyllcarotenoidinteractionsdefinesthefunctionalityoflightharvestingproteinsinplants
AT duffychristopherdp finecontrolofchlorophyllcarotenoidinteractionsdefinesthefunctionalityoflightharvestingproteinsinplants