Journal
NEURON
Volume 68, Issue 1, Pages 61-72Publisher
CELL PRESS
DOI: 10.1016/j.neuron.2010.09.001
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Funding
- National Natural Science Foundation of China [30830035, 30700145, 9091300]
- National Basic Research Program of China [2006CB500803, 2011CB809005, 2009CB918502]
- Shanghai Municipal Government [09XD1404900]
- K.C. Wong Education Foundation (Hong Kong)
- China Postdoctoral Science Foundation
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Acid-sensing ion channels (ASICs) have long been considered as extracellular proton (H+)-gated cation channels, and peripheral ASIC3 channels seem to be a natural sensor of acidic pain. Here, we report the identification of a nonproton sensor on ASIC3. We show first that 2-guanidine-4-methylquinazoline (GMQ) causes persistent ASIC3 channel activation at the normal pH. Using GMQ as a probe and combining mutagenesis and covalent modification analysis, we then uncovered a ligand sensor lined by residues around E423 and E79 of the extracellular palm domain of the ASIC3 channel that-is crucial for activation by nonproton activators. Furthermore, we show that GMQ activates sensory neurons and causes pain-related behaviors in an ASIC3,dependent manner, indicating the functional significance of ASIC activation by nonproton ligands. Thus, natural ligands beyond protons may activate ASICs under physiological and pathological conditions through the nonproton ligand sensor, serving for channel activation independent of abrupt and marked acidosis.
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