Diversity of Conus Neuropeptides
- 20 July 1990
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 249 (4966), 257-263
- https://doi.org/10.1126/science.2165278
Abstract
Conus venoms contain a remarkable diversity of pharmacologically active small peptides. Their targets are ion channels and receptors in the neuromuscular system. The venom of Conus geographus contains high-affinity peptides that act on voltage-sensitive calcium channels, sodium channels, N-methyl-D-aspartate (NMDA) receptors, acetylcholine receptors, and vasopressin receptors; many more peptides with still uncharacterized receptor targets are present in this venom. It now seems that the Conus species (approximately 500 in number) will each use a distinctive assortment of peptides and that the pharmacological diversity in Conus venoms may be ultimately comparable to that of plant alkaloids or secondary metabolites of microorganisms. The cone snails may generate this diverse spectrum of venom peptides by a "fold-lock-cut" synthetic pathway. These peptides are specific enough to discriminate effectively between closely related receptor subtypes and can be used for structure-function correlations.Keywords
This publication has 45 references indexed in Scilit:
- Peptides from Conus Venoms which Affect Ca++Entry into NeuronsJournal of Toxicology: Toxin Reviews, 1990
- Solution conformation of conotoxin GI determined by proton nuclear magnetic resonance spectroscopy and distance geometry calculationsBiochemistry, 1989
- .mu.-Conotoxin GIIIA, a peptide ligand for muscle sodium channels: chemical synthesis, radiolabeling and receptor characterizationBiochemistry, 1989
- A molluskivorous Conus toxin: conserved frameworks in conotoxinsBiochemistry, 1989
- Conus venom interaction with α2-adrenergic receptors in calf retina membranesNeurochemistry International, 1989
- A novel sodium channel inhibitor from Conus geographus: purification, structure, and pharmacological propertiesBiochemistry, 1988
- PEPTIDE TOXINS FROM VENOMOUS CONUS SNAILSAnnual Review of Biochemistry, 1988
- Comparison of two highly refined structures of bovine pancreatic trypsin inhibitorJournal of Molecular Biology, 1987
- Conotoxin GI: disulfide bridges, synthesis, and preparation of iodinated derivativesBiochemistry, 1984
- Venomous marine molluscs of the genus conusTransactions of the Royal Society of Tropical Medicine and Hygiene, 1946