Molecular Determinants of Permeation through the Cation Channel TRPV4

Abstract We have studied the molecular determinants of ion permeation through the TRPV4 channel (VRL-2, TRP12, VR-OAC, and OTRPC4). TRPV4 is characterized by both inward and outward rectification, voltage-dependent block by Ruthenium Red, a moderate selectivity for divalent versus monovalent cations, and an Eisenman IV permeability sequence. We identify two aspartate residues, Asp672 and Asp682, as important determinants of the Ca2+ sensitivity of the TRPV4 pore. Neutralization of either aspartate to alanine caused a moderate reduction of the relative permeability for divalent cations and of the degree of outward rectification. Neutralizing both aspartates simultaneously caused a much stronger reduction of Ca2+permeability and channel rectification and additionally altered the permeability order for monovalent cations toward Eisenman sequence II or I. Moreover, neutralizing Asp682 but not Asp672 strongly reduces the affinity of the channel for Ruthenium Red. Mutations to Met680, which is located at the center of a putative selectivity filter, strongly reduced whole cell current amplitude and impaired Ca2+ permeation. In contrast, neutralizing the only positively charged residue in the putative pore region, Lys675, had no obvious effects on the properties of the TRPV4 channel pore. Our findings delineate the pore region of TRPV4 and give a first insight into the possible architecture of its permeation pathway.