Structure-activity studies of cysteine-rich alpha-conotoxins that inhibit high-voltage-activated calcium channels via GABA(beta) receptor activation reveal a minimal functional motif

Abstract

alpha-Conotoxins are disulfide-rich peptides that target nicotinic acetylcholine receptors. Recently we identified several -conotoxins that also modulate voltage-gated calcium channels by acting as G protein-coupled GABA(B) receptor (GABA(B)R) agonists. These -conotoxins are promising drug leads for the treatment of chronic pain. To elucidate the diversity of -conotoxins that act through this mechanism, we synthesized and characterized a set of peptides with homology to -conotoxins known to inhibit high voltage-activated calcium channels via GABA(B)R activation. Remarkably, all disulfide isomers of the active -conotoxins Pu1.2 and Pn1.2, and the previously studied Vc1.1 showed similar levels of biological activity. Structure determination by NMR spectroscopy helped us identify a simplified biologically active eight residue peptide motif containing a single disulfide bond that is an excellent lead molecule for developing a new generation of analgesic peptide drugs