Structural plasticity and dynamic selectivity of acid-sensing ion channel-spider toxin complexes.

Publication Type:

Journal Article


Nature, Volume 489, Issue 7416, p.400-5 (2012)


Acid Sensing Ion Channels, Animals, Binding Sites, Cations, Monovalent, Cesium, Chickens, CHO Cells, Cricetinae, Crystallography, X-Ray, Hydrogen-Ion Concentration, Ion Channel Gating, Models, Molecular, Nerve Tissue Proteins, Protein Conformation, Protein Subunits, Sequence Deletion, Sodium, Sodium Channels, Spider Venoms, Spiders, Substrate Specificity


<p>Acid-sensing ion channels (ASICs) are voltage-independent, amiloride-sensitive channels involved in diverse physiological processes ranging from nociception to taste. Despite the importance of ASICs in physiology, we know little about the mechanism of channel activation. Here we show that psalmotoxin activates non-selective and Na(+)-selective currents in chicken ASIC1a at pH 7.25 and 5.5, respectively. Crystal structures of ASIC1a-psalmotoxin complexes map the toxin binding site to the extracellular domain and show how toxin binding triggers an expansion of the extracellular vestibule and stabilization of the open channel pore. At pH 7.25 the pore is approximately 10 Å in diameter, whereas at pH 5.5 the pore is largely hydrophobic and elliptical in cross-section with dimensions of approximately 5 by 7 Å, consistent with a barrier mechanism for ion selectivity. These studies define mechanisms for activation of ASICs, illuminate the basis for dynamic ion selectivity and provide the blueprints for new therapeutic agents.</p>