Biochemistry · 1987 · 342 citations · 16 references
Life SciencesNeurosciencePharmacologyNeurochemistryNeuropharmacologyNeurophysiologyCalcium SignalingCalcium-binding ProteinsIntracellular Calcium SignalingIon Channel PharmacologyVenom BiologyCa2+ SignalingCalcium Channel FunctionCalcium Channel PharmacologySnake Venom CompositionToxin BiochemistryToxin CharacterizationToxin-channel InteractionsToxin-receptor Interactions
The omega-conotoxins from the venom of fish-hunting cone snails are probably the most useful of presently available ligands for neuronal Ca channels from vertebrates. Two of these peptide toxins, omega-conotoxins MVIIA and MVIIB from the venom of Conus magus, were purified. The amino acid sequences show significant differences from omega-conotoxins from Conus geographus. Total synthesis of omega-conotoxin MVIIA was achieved, and biologically active radiolabeled toxin was produced by iodination. Although omega-conotoxins from C. geographus (GVIA) and C. magus (MVIIA) appear to compete for the same sites in mammalian brain, in amphibian brain the high-affinity binding of omega-conotoxin MVIIA has narrower specificity. In this system, it is demonstrated that a combination of two omega-conotoxins can be used for biochemically defining receptor subtypes and suggested that these correspond to subtypes of neuronal Ca2+ channels.
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George L. Ellman · Archives of Biochemistry and Biophysics · 1959 · 26.2K citations
Pehr Edman, Geoffrey S. Begg · European Journal of Biochemistry · 1967 · 2.8K citations · Full text