MmTX1 and MmTX2 from coral snake venom potently modulate GABAA receptor activity

 

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Detalles Bibliográficos
Autores: Rosso Julien, Jean Pierre, Schwarz, Jürgen R., Diaz Bustamante, Marcelo, Céard, Brigitte, Gutiérrez, José María, Kneussel, Matthias, Pongs, Olaf, Bosmans, Frank, Bougis, Pierre Edouard
Formato: artículo original
Fecha de Publicación:2015
Descripción:GABAA receptors shape synaptic transmission by modulating Cl− conductance across the cell membrane. Remarkably, animal toxins that specifically target GABAA receptors have not been identified. Here, we report the discovery of micrurotoxin1 (MmTX1) and MmTX2, two toxins present in Costa Rican coral snake venom that tightly bind to GABAA receptors at subnanomolar concentrations. Studies with recombinant and synthetic toxin variants on hippocampal neurons and cells expressing common receptor compositions suggest that MmTX1 and MmTX2 allosterically increase GABAA receptor susceptibility to agonist, thereby potentiating receptor opening as well as desensitization, possibly by interacting with the α+/β− interface. Moreover, hippocampal neuron excitability measurements reveal toxin-induced transitory network inhibition, followed by an increase in spontaneous activity. In concert, toxin injections into mouse brain result in reduced basal activity between intense seizures. Altogether, we characterized two animal toxins that enhance GABAA receptor sensitivity to agonist, thereby establishing a previously unidentified class of tools to study this receptor family.
País:Kérwá
Institución:Universidad de Costa Rica
Repositorio:Kérwá
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/30341
Acceso en línea:http://www.pnas.org/content/112/8/E891
https://hdl.handle.net/10669/30341
Palabra clave:Coral snake toxin
MmTX1
MmTX2
GABA(A) receptor
Hippocampal neurons