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Structure-Driven Pharmacology of Transient Receptor Potential Channel Vanilloid 1.

Authors :
Díaz-Franulic I
Caceres-Molina J
Sepulveda RV
Gonzalez-Nilo F
Latorre R
Source :
Molecular pharmacology [Mol Pharmacol] 2016 Sep; Vol. 90 (3), pp. 300-8. Date of Electronic Publication: 2016 Jun 22.
Publication Year :
2016

Abstract

The transient receptor potential vanilloid 1 (TRPV1) ion channel is a polymodal receptor that mediates the flux of cations across the membrane in response to several stimuli, including heat, voltage, and ligands. The best known agonist of TRPV1 channels is capsaicin, the pungent component of "hot" chili peppers. In addition, peptides found in the venom of poisonous animals, along with the lipids phosphatidylinositol 4,5-biphosphate, lysophosphatidic acid, and cholesterol, bind to TRPV1 with high affinity to modulate channel gating. Here, we discuss the functional evidence regarding ligand-dependent activation of TRPV1 channels in light of structural data recently obtained by cryoelectron microscopy. This review focuses on the mechanistic insights into ligand binding and allosteric gating of TRPV1 channels and the relevance of accurate polymodal receptor biophysical characterization for drug design in novel pain therapies.<br /> (Copyright © 2016 by The American Society for Pharmacology and Experimental Therapeutics.)

Details

Language :
English
ISSN :
1521-0111
Volume :
90
Issue :
3
Database :
MEDLINE
Journal :
Molecular pharmacology
Publication Type :
Academic Journal
Accession number :
27335334
Full Text :
https://doi.org/10.1124/mol.116.104430