Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations.

Vision is the dominant sensory modality in many organisms for foraging, predator avoidance, and social behaviors including mate selection. Vertebrate visual perception is initiated when light strikes rod and cone photoreceptors within the neural retina of the eye. Sensitivity to individual colors, i...

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Main Authors: Jagdish Suresh Patel, Celeste J Brown, F Marty Ytreberg, Deborah L Stenkamp
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC5798944?pdf=render
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author Jagdish Suresh Patel
Celeste J Brown
F Marty Ytreberg
Deborah L Stenkamp
author_facet Jagdish Suresh Patel
Celeste J Brown
F Marty Ytreberg
Deborah L Stenkamp
author_sort Jagdish Suresh Patel
collection DOAJ
description Vision is the dominant sensory modality in many organisms for foraging, predator avoidance, and social behaviors including mate selection. Vertebrate visual perception is initiated when light strikes rod and cone photoreceptors within the neural retina of the eye. Sensitivity to individual colors, i.e., peak spectral sensitivities (λmax) of visual pigments, are a function of the type of chromophore and the amino acid sequence of the associated opsin protein in the photoreceptors. Large differences in peak spectral sensitivities can result from minor differences in amino acid sequence of cone opsins. To determine how minor sequence differences could result in large spectral shifts we selected a spectrally-diverse group of 14 teleost Rh2 cone opsins for which sequences and λmax are experimentally known. Classical molecular dynamics simulations were carried out after embedding chromophore-associated homology structures within explicit bilayers and water. These simulations revealed structural features of visual pigments, particularly within the chromophore, that contributed to diverged spectral sensitivities. Statistical tests performed on all the observed structural parameters associated with the chromophore revealed that a two-term, first-order regression model was sufficient to accurately predict λmax over a range of 452-528 nm. The approach was accurate, efficient and simple in that site-by-site molecular modifications or complex quantum mechanics models were not required to predict λmax. These studies identify structural features associated with the chromophore that may explain diverged spectral sensitivities, and provide a platform for future, functionally predictive opsin modeling.
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spelling doaj.art-92e0d6f2d79349cb8b95dd8a78c6f5542022-12-22T01:09:20ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582018-01-01141e100597410.1371/journal.pcbi.1005974Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations.Jagdish Suresh PatelCeleste J BrownF Marty YtrebergDeborah L StenkampVision is the dominant sensory modality in many organisms for foraging, predator avoidance, and social behaviors including mate selection. Vertebrate visual perception is initiated when light strikes rod and cone photoreceptors within the neural retina of the eye. Sensitivity to individual colors, i.e., peak spectral sensitivities (λmax) of visual pigments, are a function of the type of chromophore and the amino acid sequence of the associated opsin protein in the photoreceptors. Large differences in peak spectral sensitivities can result from minor differences in amino acid sequence of cone opsins. To determine how minor sequence differences could result in large spectral shifts we selected a spectrally-diverse group of 14 teleost Rh2 cone opsins for which sequences and λmax are experimentally known. Classical molecular dynamics simulations were carried out after embedding chromophore-associated homology structures within explicit bilayers and water. These simulations revealed structural features of visual pigments, particularly within the chromophore, that contributed to diverged spectral sensitivities. Statistical tests performed on all the observed structural parameters associated with the chromophore revealed that a two-term, first-order regression model was sufficient to accurately predict λmax over a range of 452-528 nm. The approach was accurate, efficient and simple in that site-by-site molecular modifications or complex quantum mechanics models were not required to predict λmax. These studies identify structural features associated with the chromophore that may explain diverged spectral sensitivities, and provide a platform for future, functionally predictive opsin modeling.http://europepmc.org/articles/PMC5798944?pdf=render
spellingShingle Jagdish Suresh Patel
Celeste J Brown
F Marty Ytreberg
Deborah L Stenkamp
Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations.
PLoS Computational Biology
title Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations.
title_full Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations.
title_fullStr Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations.
title_full_unstemmed Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations.
title_short Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations.
title_sort predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations
url http://europepmc.org/articles/PMC5798944?pdf=render
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