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Exciton Lifetime Distributions and Population Dynamics in the FMO Protein Complex from Prosthecochloris aestuarii
[Image: see text] Significant protein rearrangement upon excitation and energy transfer in Fenna–Matthews–Olson protein of Prosthecochloris aestuarii results in a modified energy landscape, which induces more changes in pigment site energies than predicted by the “standard” hole-burning theory. The...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7931385/ https://www.ncbi.nlm.nih.gov/pubmed/33681637 http://dx.doi.org/10.1021/acsomega.1c00286 |
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author | Reinot, Tonu Khmelnitskiy, Anton Kell, Adam Jassas, Mahboobe Jankowiak, Ryszard |
author_facet | Reinot, Tonu Khmelnitskiy, Anton Kell, Adam Jassas, Mahboobe Jankowiak, Ryszard |
author_sort | Reinot, Tonu |
collection | PubMed |
description | [Image: see text] Significant protein rearrangement upon excitation and energy transfer in Fenna–Matthews–Olson protein of Prosthecochloris aestuarii results in a modified energy landscape, which induces more changes in pigment site energies than predicted by the “standard” hole-burning theory. The energy changes are elucidated by simulations while investigating the effects of site-dependent disorder, both static (site-energy distribution widths) and dynamic (spectral density shapes). The resulting optimized site energies and their fluctuations are consistent with relative differences observed in inhomogeneous widths calculated by recent molecular dynamic simulations. Two sets of different spectral densities reveal how their shapes affect the population dynamics and distribution of exciton lifetimes. Calculations revealed the wavelength-dependent distributions of exciton lifetimes (T(1)) in the femtosecond to picosecond time frame. We suggest that the calculated multimodal and asymmetric wavelength-dependent T(1) distributions offer more insight into the interpretation of resonant hole-burned (HB) spectra, kinetic traces in two-dimensional (2D) electronic spectroscopy experiments, and widely used global analyses in fitting data from transient absorption experiments. |
format | Online Article Text |
id | pubmed-7931385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79313852021-03-05 Exciton Lifetime Distributions and Population Dynamics in the FMO Protein Complex from Prosthecochloris aestuarii Reinot, Tonu Khmelnitskiy, Anton Kell, Adam Jassas, Mahboobe Jankowiak, Ryszard ACS Omega [Image: see text] Significant protein rearrangement upon excitation and energy transfer in Fenna–Matthews–Olson protein of Prosthecochloris aestuarii results in a modified energy landscape, which induces more changes in pigment site energies than predicted by the “standard” hole-burning theory. The energy changes are elucidated by simulations while investigating the effects of site-dependent disorder, both static (site-energy distribution widths) and dynamic (spectral density shapes). The resulting optimized site energies and their fluctuations are consistent with relative differences observed in inhomogeneous widths calculated by recent molecular dynamic simulations. Two sets of different spectral densities reveal how their shapes affect the population dynamics and distribution of exciton lifetimes. Calculations revealed the wavelength-dependent distributions of exciton lifetimes (T(1)) in the femtosecond to picosecond time frame. We suggest that the calculated multimodal and asymmetric wavelength-dependent T(1) distributions offer more insight into the interpretation of resonant hole-burned (HB) spectra, kinetic traces in two-dimensional (2D) electronic spectroscopy experiments, and widely used global analyses in fitting data from transient absorption experiments. American Chemical Society 2021-02-19 /pmc/articles/PMC7931385/ /pubmed/33681637 http://dx.doi.org/10.1021/acsomega.1c00286 Text en © 2021 The Authors. Published by American Chemical Society This is an open access article published under an ACS AuthorChoice License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Reinot, Tonu Khmelnitskiy, Anton Kell, Adam Jassas, Mahboobe Jankowiak, Ryszard Exciton Lifetime Distributions and Population Dynamics in the FMO Protein Complex from Prosthecochloris aestuarii |
title | Exciton Lifetime Distributions and Population Dynamics
in the FMO Protein Complex from Prosthecochloris aestuarii |
title_full | Exciton Lifetime Distributions and Population Dynamics
in the FMO Protein Complex from Prosthecochloris aestuarii |
title_fullStr | Exciton Lifetime Distributions and Population Dynamics
in the FMO Protein Complex from Prosthecochloris aestuarii |
title_full_unstemmed | Exciton Lifetime Distributions and Population Dynamics
in the FMO Protein Complex from Prosthecochloris aestuarii |
title_short | Exciton Lifetime Distributions and Population Dynamics
in the FMO Protein Complex from Prosthecochloris aestuarii |
title_sort | exciton lifetime distributions and population dynamics
in the fmo protein complex from prosthecochloris aestuarii |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7931385/ https://www.ncbi.nlm.nih.gov/pubmed/33681637 http://dx.doi.org/10.1021/acsomega.1c00286 |
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