Molecular basis for pore blockade of human Na⁺ channel Na_v1.2 by the μ-conotoxin KIIIA.

Abstract

The voltage-gated sodium channel Na_v1.2 is responsible for the initiation and propagation of action potentials in the central nervous system. We report the cryo-electron microscopy structure of human Na_v1.2 bound to a peptidic pore blocker, the μ-conotoxin KIIIA, in the presence of an auxiliary subunit, β2, to an overall resolution of 3.0 angstroms. The immunoglobulin domain of β2 interacts with the shoulder of the pore domain through a disulfide bond. The 16-residue KIIIA interacts with the extracellular segments in repeats I to III, placing Lys⁷ at the entrance to the selectivity filter. Many interacting residues are specific to Na_v1.2, revealing a molecular basis for KIIIA specificity. The structure establishes a framework for the rational design of subtype-specific blockers for Na_v channels.