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Characterization of a Novel Gastropod Toxin (6-Bromo-2-mercaptotryptamine) That Inhibits Shaker K Channel Activity

A novel potassium channel antagonist has been purified from the defensive mucus secreted by Calliostoma canaliculatum, a marine snail found in the temperate coastal waters of the western Pacific. The toxin is expelled from the hypobranchial gland as part of a defensive response and is contained with...

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Published in:The Journal of biological chemistry 2003-09, Vol.278 (37), p.34934-34942
Main Authors: Kelley, Wayne P., Wolters, Andrew M., Sack, Jon T., Jockusch, Rebecca A., Jurchen, John C., Williams, Evan R., Sweedler, Jonathan V., Gilly, William F.
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cited_by cdi_FETCH-LOGICAL-c409t-9264ebdb43e381b00c97b517a1ca0955e5cba99992e5e64b7dc45e84325d42983
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container_end_page 34942
container_issue 37
container_start_page 34934
container_title The Journal of biological chemistry
container_volume 278
creator Kelley, Wayne P.
Wolters, Andrew M.
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description A novel potassium channel antagonist has been purified from the defensive mucus secreted by Calliostoma canaliculatum, a marine snail found in the temperate coastal waters of the western Pacific. The toxin is expelled from the hypobranchial gland as part of a defensive response and is contained within a viscous matrix that minimizes dilution and degradation. The active compound was isolated by multistage microbore HPLC separations followed by bioactivity assays. Nuclear magnetic resonance, combined with electrospray ionization Fourier-transform ion cyclotron resonance and electrospray ionization ion trap mass spectrometry indicate that the active component is a heretofore unknown indole-derivative, a disulfide-linked dimer of 6-bromo-2-mercaptotryptamine (BrMT). Exudates from the hypobranchial glands of various marine mollusks have been sources for dye compounds such as 6–6 dibromoindigo, the ancient dye Tyrian purple. BrMT represents the first correlation of a hypobranchial gland exudate with a molecular response. Voltage clamp experiments with a number of K channel subtypes indicate that BrMT inhibits certain voltage-gated K channels of the Kv1 subfamily.
doi_str_mv 10.1074/jbc.M301271200
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identifier ISSN: 0021-9258
ispartof The Journal of biological chemistry, 2003-09, Vol.278 (37), p.34934-34942
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recordid cdi_proquest_miscellaneous_18940594
source ScienceDirect®
subjects 6-bromo-2-mercaptotryptamine
Animals
Calliostoma canaliculatum
Chromatography, High Pressure Liquid
Disulfides - chemistry
Disulfides - isolation & purification
Disulfides - pharmacology
Female
hypobranchial gland
Magnetic Resonance Spectroscopy
Marine
Oocytes - drug effects
Oocytes - physiology
Potassium Channel Blockers - chemistry
Potassium Channel Blockers - isolation & purification
Potassium Channel Blockers - pharmacology
potassium channels
Potassium Channels - physiology
Recombinant Proteins - drug effects
Shaker Superfamily of Potassium Channels
Snails
Spectrometry, Mass, Electrospray Ionization
Tryptamines - chemistry
Tryptamines - isolation & purification
Tryptamines - pharmacology
Xenopus laevis
title Characterization of a Novel Gastropod Toxin (6-Bromo-2-mercaptotryptamine) That Inhibits Shaker K Channel Activity
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