Definition of two agonist types at the mammalian cold-activated channel TRPM8
Annelies Janssens,
Maarten Gees,
Balazs Istvan Toth,
Debapriya Ghosh,
Marie Mulier,
Rudi Vennekens,
Joris Vriens,
Karel Talavera,
Thomas Voets
Affiliations
Annelies Janssens
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium
Maarten Gees
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium
Balazs Istvan Toth
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium
Debapriya Ghosh
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium
Marie Mulier
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium
Rudi Vennekens
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium
Joris Vriens
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium; Laboratory of Experimental Gynaecology, University of Leuven, Leuven, Belgium
Karel Talavera
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium
Laboratory of Ion Channel Research and TRP channel Research Platform Leuven, Department of Cellular and Molecular Medicine, University of Leuven, Leuven, Belgium
Various TRP channels act as polymodal sensors of thermal and chemical stimuli, but the mechanisms whereby chemical ligands impact on TRP channel gating are poorly understood. Here we show that AITC (allyl isothiocyanate; mustard oil) and menthol represent two distinct types of ligands at the mammalian cold sensor TRPM8. Kinetic analysis of channel gating revealed that AITC acts by destabilizing the closed channel, whereas menthol stabilizes the open channel, relative to the transition state. Based on these differences, we classify agonists as either type I (menthol-like) or type II (AITC-like), and provide a kinetic model that faithfully reproduces their differential effects. We further demonstrate that type I and type II agonists have a distinct impact on TRPM8 currents and TRPM8-mediated calcium signals in excitable cells. These findings provide a theoretical framework for understanding the differential actions of TRP channel ligands, with important ramifications for TRP channel structure-function analysis and pharmacology.