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Theory of FRET “Spectroscopic Ruler” for Short Distances: Application to Polyproline
[Image: see text] Förster resonance energy transfer (FRET) is an important mechanism for the estimation of intermolecular distances, e.g., in fluorescent labeled proteins. The interpretations of FRET experiments with standard Förster theory relies on the following approximations: (i) a point-dipole...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767878/ https://www.ncbi.nlm.nih.gov/pubmed/29189003 http://dx.doi.org/10.1021/acs.jpcb.7b09535 |
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author | Sobakinskaya, Ekaterina Schmidt am Busch, Marcel Renger, Thomas |
author_facet | Sobakinskaya, Ekaterina Schmidt am Busch, Marcel Renger, Thomas |
author_sort | Sobakinskaya, Ekaterina |
collection | PubMed |
description | [Image: see text] Förster resonance energy transfer (FRET) is an important mechanism for the estimation of intermolecular distances, e.g., in fluorescent labeled proteins. The interpretations of FRET experiments with standard Förster theory relies on the following approximations: (i) a point-dipole approximation (PDA) for the coupling between transition densities of the chromophores, (ii) a screening of this coupling by the inverse optical dielectric constant of the medium, and (iii) the assumption of fast isotropic sampling over the mutual orientations of the chromophores. These approximations become critical, in particular, at short intermolecular distances, where the PDA and the screening model become invalid and the variation of interchromophore distances, and not just orientations, has a critical influence on the excitation energy transfer. Here, we present a quantum chemical/electrostatic/molecular dynamics (MD) method that goes beyond all of the above approximations. The Poisson-TrEsp method for the ab initio/electrostatic calculation of excitonic couplings in a dielectric medium is combined with all-atom molecular dynamics (MD) simulations to calculate FRET efficiencies. The method is applied to analyze single-molecule experiments on a polyproline helix of variable length labeled with Alexa dyes. Our method provides a quantitative explanation of the overestimation of FRET efficiencies by the standard Förster theory for short interchromophore distances for this system. A detailed analysis of the different levels of approximation that connect the present Poisson-TrEsp/MD method with Förster theory reveals error compensation effects, between the PDA and the neglect of correlations in interchromophore distances and orientations on one hand and the neglect of static disorder in orientations and interchromophore distances on the other. Whereas the first two approximations are found to decrease the FRET efficiency, the latter two overcompensate this decrease and are responsible for the overestimation of the FRET efficiency by Förster theory. |
format | Online Article Text |
id | pubmed-5767878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-57678782018-01-16 Theory of FRET “Spectroscopic Ruler” for Short Distances: Application to Polyproline Sobakinskaya, Ekaterina Schmidt am Busch, Marcel Renger, Thomas J Phys Chem B [Image: see text] Förster resonance energy transfer (FRET) is an important mechanism for the estimation of intermolecular distances, e.g., in fluorescent labeled proteins. The interpretations of FRET experiments with standard Förster theory relies on the following approximations: (i) a point-dipole approximation (PDA) for the coupling between transition densities of the chromophores, (ii) a screening of this coupling by the inverse optical dielectric constant of the medium, and (iii) the assumption of fast isotropic sampling over the mutual orientations of the chromophores. These approximations become critical, in particular, at short intermolecular distances, where the PDA and the screening model become invalid and the variation of interchromophore distances, and not just orientations, has a critical influence on the excitation energy transfer. Here, we present a quantum chemical/electrostatic/molecular dynamics (MD) method that goes beyond all of the above approximations. The Poisson-TrEsp method for the ab initio/electrostatic calculation of excitonic couplings in a dielectric medium is combined with all-atom molecular dynamics (MD) simulations to calculate FRET efficiencies. The method is applied to analyze single-molecule experiments on a polyproline helix of variable length labeled with Alexa dyes. Our method provides a quantitative explanation of the overestimation of FRET efficiencies by the standard Förster theory for short interchromophore distances for this system. A detailed analysis of the different levels of approximation that connect the present Poisson-TrEsp/MD method with Förster theory reveals error compensation effects, between the PDA and the neglect of correlations in interchromophore distances and orientations on one hand and the neglect of static disorder in orientations and interchromophore distances on the other. Whereas the first two approximations are found to decrease the FRET efficiency, the latter two overcompensate this decrease and are responsible for the overestimation of the FRET efficiency by Förster theory. American Chemical Society 2017-11-30 2018-01-11 /pmc/articles/PMC5767878/ /pubmed/29189003 http://dx.doi.org/10.1021/acs.jpcb.7b09535 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Sobakinskaya, Ekaterina Schmidt am Busch, Marcel Renger, Thomas Theory of FRET “Spectroscopic Ruler” for Short Distances: Application to Polyproline |
title | Theory of FRET “Spectroscopic Ruler”
for Short Distances: Application to Polyproline |
title_full | Theory of FRET “Spectroscopic Ruler”
for Short Distances: Application to Polyproline |
title_fullStr | Theory of FRET “Spectroscopic Ruler”
for Short Distances: Application to Polyproline |
title_full_unstemmed | Theory of FRET “Spectroscopic Ruler”
for Short Distances: Application to Polyproline |
title_short | Theory of FRET “Spectroscopic Ruler”
for Short Distances: Application to Polyproline |
title_sort | theory of fret “spectroscopic ruler”
for short distances: application to polyproline |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767878/ https://www.ncbi.nlm.nih.gov/pubmed/29189003 http://dx.doi.org/10.1021/acs.jpcb.7b09535 |
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