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An Analysis of the Putative CBD Binding Site in the Ionotropic Cannabinoid Receptors

Cannabinoids have been long studied for their therapeutic properties, particularly for their use in the treatment of pain. As new therapies are sought after to treat conditions of chronic pain, so is a better understanding of the ligands and their target receptors or channels. A recently published c...

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Autores principales: Muller, Chanté, Reggio, Patricia H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755602/
https://www.ncbi.nlm.nih.gov/pubmed/33362478
http://dx.doi.org/10.3389/fncel.2020.615811
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author Muller, Chanté
Reggio, Patricia H.
author_facet Muller, Chanté
Reggio, Patricia H.
author_sort Muller, Chanté
collection PubMed
description Cannabinoids have been long studied for their therapeutic properties, particularly for their use in the treatment of pain. As new therapies are sought after to treat conditions of chronic pain, so is a better understanding of the ligands and their target receptors or channels. A recently published cryo-EM structure showed the putative binding location of a well-known cannabinoid ligand, cannabidiol (CBD), in TRPV2, a channel that has been implicated in inflammation and chronic pain. TRPV2, along with TRPV1, TRPV3, TRPV4, TRPA1, and TRPM8 all have the capability to be modulated by cannabinoid ligands and are located in the peripheral nervous system. Here, we analyze the putative CBD binding site in each of these channels and compare structural and sequential information with experimental data.
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spelling pubmed-77556022020-12-24 An Analysis of the Putative CBD Binding Site in the Ionotropic Cannabinoid Receptors Muller, Chanté Reggio, Patricia H. Front Cell Neurosci Cellular Neuroscience Cannabinoids have been long studied for their therapeutic properties, particularly for their use in the treatment of pain. As new therapies are sought after to treat conditions of chronic pain, so is a better understanding of the ligands and their target receptors or channels. A recently published cryo-EM structure showed the putative binding location of a well-known cannabinoid ligand, cannabidiol (CBD), in TRPV2, a channel that has been implicated in inflammation and chronic pain. TRPV2, along with TRPV1, TRPV3, TRPV4, TRPA1, and TRPM8 all have the capability to be modulated by cannabinoid ligands and are located in the peripheral nervous system. Here, we analyze the putative CBD binding site in each of these channels and compare structural and sequential information with experimental data. Frontiers Media S.A. 2020-12-09 /pmc/articles/PMC7755602/ /pubmed/33362478 http://dx.doi.org/10.3389/fncel.2020.615811 Text en Copyright © 2020 Muller and Reggio. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Muller, Chanté
Reggio, Patricia H.
An Analysis of the Putative CBD Binding Site in the Ionotropic Cannabinoid Receptors
title An Analysis of the Putative CBD Binding Site in the Ionotropic Cannabinoid Receptors
title_full An Analysis of the Putative CBD Binding Site in the Ionotropic Cannabinoid Receptors
title_fullStr An Analysis of the Putative CBD Binding Site in the Ionotropic Cannabinoid Receptors
title_full_unstemmed An Analysis of the Putative CBD Binding Site in the Ionotropic Cannabinoid Receptors
title_short An Analysis of the Putative CBD Binding Site in the Ionotropic Cannabinoid Receptors
title_sort analysis of the putative cbd binding site in the ionotropic cannabinoid receptors
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755602/
https://www.ncbi.nlm.nih.gov/pubmed/33362478
http://dx.doi.org/10.3389/fncel.2020.615811
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