Voltage-Gated Sodium Channel Inhibition by µ-Conotoxins

Author:

McMahon Kirsten L.1,Vetter Irina12ORCID,Schroeder Christina I.13ORCID

Affiliation:

1. Institute for Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia

2. The School of Pharmacy, The University of Queensland, Woolloongabba, QLD 4102, Australia

3. Genentech, 1 DNA Way, South San Francisco, CA 94080, USA

Abstract

µ-Conotoxins are small, potent pore-blocker inhibitors of voltage-gated sodium (NaV) channels, which have been identified as pharmacological probes and putative leads for analgesic development. A limiting factor in their therapeutic development has been their promiscuity for different NaV channel subtypes, which can lead to undesirable side-effects. This review will focus on four areas of µ-conotoxin research: (1) mapping the interactions of µ-conotoxins with different NaV channel subtypes, (2) µ-conotoxin structure–activity relationship studies, (3) observed species selectivity of µ-conotoxins and (4) the effects of µ-conotoxin disulfide connectivity on activity. Our aim is to provide a clear overview of the current status of µ-conotoxin research.

Funder

Australian National Health and Medical Research Council

University of Queensland

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Toxicology

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