Transient receptor potential ankyrin 1 (TRPA1) is a temperature-sensitive ion channel activated by various pungent and irritant compounds that can produce pain in humans. Its activation involves an allosteric mechanism whereby electrophilic agonists evoke interactions within cytosolic domains and open the channel pore through an integrated nexus formed by intracellular membrane proximal regions that are densely packed beneath the lower segment of the S1-S4 sensor domain. Studies indicate that this part of the channel may contain residues that form a water-accessible cavity that undergoes changes in solvation during channel gating. We identified conserved polar residues facing the putative lower crevice of the sensor domain that were crucial determinants of the electrophilic, voltage, and calcium sensitivity of the TRPA1 channel. This part of the sensor may also comprise a domain capable of binding to membrane phosphoinositides through which gating of the channel is regulated in a state-dependent manner.

Department of Cellular Neurophysiology Institute of Physiology Czech Academy of Sciences 14220 Prague Czech Republic

Division of Biomolecular Physics Institute of Physics Faculty of Mathematics and Physics Charles University 12116 Prague Czech Republic

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$a Zimova, Lucie $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, 14220 Prague, Czech Republic.

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$a Intracellular cavity of sensor domain controls allosteric gating of TRPA1 channel / $c L. Zimova, V. Sinica, A. Kadkova, L. Vyklicka, V. Zima, I. Barvik, V. Vlachova,

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$a Transient receptor potential ankyrin 1 (TRPA1) is a temperature-sensitive ion channel activated by various pungent and irritant compounds that can produce pain in humans. Its activation involves an allosteric mechanism whereby electrophilic agonists evoke interactions within cytosolic domains and open the channel pore through an integrated nexus formed by intracellular membrane proximal regions that are densely packed beneath the lower segment of the S1-S4 sensor domain. Studies indicate that this part of the channel may contain residues that form a water-accessible cavity that undergoes changes in solvation during channel gating. We identified conserved polar residues facing the putative lower crevice of the sensor domain that were crucial determinants of the electrophilic, voltage, and calcium sensitivity of the TRPA1 channel. This part of the sensor may also comprise a domain capable of binding to membrane phosphoinositides through which gating of the channel is regulated in a state-dependent manner.

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$a Sinica, Viktor $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, 14220 Prague, Czech Republic.

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$a Kadkova, Anna $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, 14220 Prague, Czech Republic.

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$a Vyklicka, Lenka $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, 14220 Prague, Czech Republic.

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$a Zima, Vlastimil $u Division of Biomolecular Physics, Institute of Physics, Faculty of Mathematics and Physics, Charles University, 12116 Prague, Czech Republic.

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$a Barvik, Ivan $u Division of Biomolecular Physics, Institute of Physics, Faculty of Mathematics and Physics, Charles University, 12116 Prague, Czech Republic.

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$a Vlachova, Viktorie $u Department of Cellular Neurophysiology, Institute of Physiology Czech Academy of Sciences, 14220 Prague, Czech Republic. viktorie.vlachova@fgu.cas.cz.

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