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Inhibition of Sodium Ion Channel Function with Truncated Forms of Batrachotoxin.
Toma, Tatsuya; Logan, Matthew M; Menard, Frederic; Devlin, A Sloan; Du Bois, J.
Afiliação
  • Toma T; Department of Chemistry, Stanford University , Stanford, California 94305-5080, United States.
  • Logan MM; Department of Chemistry, Stanford University , Stanford, California 94305-5080, United States.
  • Menard F; Department of Chemistry, Stanford University , Stanford, California 94305-5080, United States.
  • Devlin AS; Department of Chemistry, Stanford University , Stanford, California 94305-5080, United States.
  • Du Bois J; Department of Chemistry, Stanford University , Stanford, California 94305-5080, United States.
ACS Chem Neurosci ; 7(10): 1463-1468, 2016 10 19.
Article em En | MEDLINE | ID: mdl-27501251
A novel family of small molecule inhibitors of voltage-gated sodium channels (NaVs) based on the structure of batrachotoxin (BTX), a well-known channel agonist, is described. Protein mutagenesis and electrophysiology experiments reveal the binding site as the inner pore region of the channel, analogous to BTX, alkaloid toxins, and local anesthetics. Homology modeling of the eukaryotic channel based on recent crystallographic analyses of bacterial NaVs suggests a mechanism of action for ion conduction block.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Batraquiotoxinas / Bloqueadores dos Canais de Sódio Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Batraquiotoxinas / Bloqueadores dos Canais de Sódio Idioma: En Ano de publicação: 2016 Tipo de documento: Article