Structure/function characterization of μ-conotoxin KIIIA, an analgesic, nearly irreversible blocker of mammalian neuronal sodium channels

Min Min Zhang, Brad R. Green, Philip Catlin, Brian Fiedler, Layla Azam, Ashley Chadwick, Heinrich Terlau, Jeff R. McArthur, Robert J. French, Josef Gulyas, Jean E. Rivier, Brian J. Smith, Raymond S. Norton, Baldomero M. Olivera, Doju Yoshikami, Grzegorz Bulaj

Research output: Contribution to journalArticleResearchpeer-review

104 Citations (Scopus)

Abstract

Peptide neurotoxins from cone snails continue to supply compounds with therapeutic potential. Although several analgesic conotoxins have already reached human clinical trials, a continuing need exists for the discovery and development of novel nonopioid analgesics, such as subtype-selective sodium channel blockers. μ-Conotoxin KIIIA is representative of μ-conopeptides previously characterized as inhibitors of tetrodotoxin (TTX)-resistant sodium channels in amphibian dorsal root ganglion neurons. Here, we show that KIIIA has potent analgesic activity in the mouse pain model. Surprisingly, KIIIA was found to block most (>80%) of the TTX-sensitive, but only ∼20% of the TTX-resistant, sodium current in mouse dorsal root ganglion neurons. KIIIA was tested on cloned mammalian channels expressed in Xenopus oocytes. Both Na V1.2 and NaV1.6 were strongly blocked; within experimental wash times of 40-60 min, block was reversed very little for NaV1.2 and only partially for NaV1.6. Other isoforms were blocked reversibly: NaV1.3 (IC50 8 μM), NaV1.5 (IC50 284 μM), and NaV1.4 (IC50 80 nM). "Alanine-walk" and related analogs were synthesized and tested against both NaV1.2 and NaV1.4; replacement of Trp-8 resulted in reversible block of NaV1.2, whereas replacement of Lys-7, Trp-8, or Asp-11 yielded a more profound effect on the block of NaV1.4 than of NaV1.2. Taken together, these data suggest that KIIIA is an effective tool to study structure and function of NaV1.2 and that further engineering of μ-conopeptides belonging to the KIIIA group may provide subtype-selective pharmacological compounds for mammalian neuronal sodium channels and potential therapeutics for the treatment of pain.

Original languageEnglish
Pages (from-to)30699-30706
Number of pages8
JournalThe Journal of Biological Chemistry
Volume282
Issue number42
DOIs
Publication statusPublished - 19 Oct 2007
Externally publishedYes

Cite this

Zhang, M. M., Green, B. R., Catlin, P., Fiedler, B., Azam, L., Chadwick, A., Terlau, H., McArthur, J. R., French, R. J., Gulyas, J., Rivier, J. E., Smith, B. J., Norton, R. S., Olivera, B. M., Yoshikami, D., & Bulaj, G. (2007). Structure/function characterization of μ-conotoxin KIIIA, an analgesic, nearly irreversible blocker of mammalian neuronal sodium channels. The Journal of Biological Chemistry, 282(42), 30699-30706. https://doi.org/10.1074/jbc.M704616200