A designer saxitoxin-engineered sodium channel pair as a general tool for subtype-selective inhibition

Abstract

SUMMARY We have used small molecule chemical design and protein engineering to fashion an orthogonal ligand-channel pair that enables acute and selective inhibition of a genetically encoded voltage-gated sodium channel (NaV). A modified ligand based on the nerve toxin, saxitoxin (STX), binds potently and reversibly to a NaV bearing two unique amino acid mutations in the outer mouth of the channel (Site 1). The same ligand is ineffective at blocking wild-type NaVs and does not disrupt action potential signals in neuronal cells or brain tissue at working concentrations. The versatility of this tool derives from the highly conserved outer pore (Site 1), as the same two amino acid replacements can be introduced in NaV1.1–1.4, 1.6, or 1.7, thus sensitizing each channel to inhibition by the designer STX ligand. This tool will empower studies of NaV-isoform physiology to better understand the role of NaVs in health and disease.