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Evaluating Allosteric Perturbations in Cannabinoid Receptor 1 by In Silico Single-Point Mutation

[Image: see text] Cannabinoid receptor 1 (CB1) is a promising drug target involved in many physiological processes. Using atomistic molecular dynamics (MD) simulations, we examined the structural effect of F237L mutation on CB1, a mutation that has qualitatively similar effects to allosteric ligand...

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Autores principales: Díaz, Oscar, Renault, Pedro, Giraldo, Jesús
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608382/
https://www.ncbi.nlm.nih.gov/pubmed/36312415
http://dx.doi.org/10.1021/acsomega.2c04980
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author Díaz, Oscar
Renault, Pedro
Giraldo, Jesús
author_facet Díaz, Oscar
Renault, Pedro
Giraldo, Jesús
author_sort Díaz, Oscar
collection PubMed
description [Image: see text] Cannabinoid receptor 1 (CB1) is a promising drug target involved in many physiological processes. Using atomistic molecular dynamics (MD) simulations, we examined the structural effect of F237L mutation on CB1, a mutation that has qualitatively similar effects to allosteric ligand ORG27569 binding. This mutation showed a global effect on CB1 conformations. Among the observed effects, TM6 outward movement and the conformational change of the NPxxY motif upon receptor activation by CB1 agonist CP55940 were hindered compared to wt CB1. Within the orthosteric binding site, CP55940 interactions with CB1 were altered. Our results revealed that allosteric perturbations introduced by the mutation had a global impact on receptor conformations, suggesting that the mutation site is a key region for allosteric modulation in CB1.
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spelling pubmed-96083822022-10-28 Evaluating Allosteric Perturbations in Cannabinoid Receptor 1 by In Silico Single-Point Mutation Díaz, Oscar Renault, Pedro Giraldo, Jesús ACS Omega [Image: see text] Cannabinoid receptor 1 (CB1) is a promising drug target involved in many physiological processes. Using atomistic molecular dynamics (MD) simulations, we examined the structural effect of F237L mutation on CB1, a mutation that has qualitatively similar effects to allosteric ligand ORG27569 binding. This mutation showed a global effect on CB1 conformations. Among the observed effects, TM6 outward movement and the conformational change of the NPxxY motif upon receptor activation by CB1 agonist CP55940 were hindered compared to wt CB1. Within the orthosteric binding site, CP55940 interactions with CB1 were altered. Our results revealed that allosteric perturbations introduced by the mutation had a global impact on receptor conformations, suggesting that the mutation site is a key region for allosteric modulation in CB1. American Chemical Society 2022-10-14 /pmc/articles/PMC9608382/ /pubmed/36312415 http://dx.doi.org/10.1021/acsomega.2c04980 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Díaz, Oscar
Renault, Pedro
Giraldo, Jesús
Evaluating Allosteric Perturbations in Cannabinoid Receptor 1 by In Silico Single-Point Mutation
title Evaluating Allosteric Perturbations in Cannabinoid Receptor 1 by In Silico Single-Point Mutation
title_full Evaluating Allosteric Perturbations in Cannabinoid Receptor 1 by In Silico Single-Point Mutation
title_fullStr Evaluating Allosteric Perturbations in Cannabinoid Receptor 1 by In Silico Single-Point Mutation
title_full_unstemmed Evaluating Allosteric Perturbations in Cannabinoid Receptor 1 by In Silico Single-Point Mutation
title_short Evaluating Allosteric Perturbations in Cannabinoid Receptor 1 by In Silico Single-Point Mutation
title_sort evaluating allosteric perturbations in cannabinoid receptor 1 by in silico single-point mutation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608382/
https://www.ncbi.nlm.nih.gov/pubmed/36312415
http://dx.doi.org/10.1021/acsomega.2c04980
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