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CalcicludineCalcicludine (CaC) is a protein toxin from the venom of the green mamba that inhibits high-voltage-activated calcium channels, especially L-type calcium channels. Additional recommended knowledge
SourceCalcicludine is a toxin in the venom of the green mamba (Dendroaspis angusticeps). ChemistryCalcicludine is a 60-amino acid polypeptide with six cysteines forming three disulfide bridges. Calcicludine structurally resembles dendrotoxin, but works differently, since even at high concentrations, calcicludine has no effect on dendrotoxin-sensitive potassium channels in chicken and rat neurons.[1] TargetCalcicludine is a blocker of high-voltage-activated calcium channels (L-, N- and P-type channels). It has highest affinity to the L-type calcium channel (IC50 = 88nM[2]). However, sensitivity of the drug on the channel depends on the species and the tissue. For example, the IC50 for block of L-type calcium channels on a cerebellar granule cell is 0.2 nM, but the IC50 of the block of rat peripheral DRG neuronal L-type channels is around 60-80 nM.[1] Mode of ActionCalcicludine has a unique mode of action, which is still incompletely understood. It has been suggested to act by a partial pore block or an effect on channel gating.[2] ToxicityCalcicludine has been shown to work on rat cardiac cells and rat cerebellum granule cells.[1] References[1]: Calcicludine, A Venom Peptide of the Kunitz-Type Protease Inhibitor Family, is a Potent Blocker of High-Threshold Ca 2+ Channels with a High Affinity for L-Type Channels in Cerebellar Granule Neurons, Schweitz et al., 1994 Categories: Neurotoxins | Toxicology | Ion channel toxins |
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This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Calcicludine". A list of authors is available in Wikipedia. |