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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...

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Autores principales: Sobakinskaya, Ekaterina, Schmidt am Busch, Marcel, Renger, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
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.
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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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