Cargando…
Characterisation of δ-Conotoxin TxVIA as a Mammalian T-Type Calcium Channel Modulator
The 27-amino acid (aa)-long δ-conotoxin TxVIA, originally isolated from the mollusc-hunting cone snail Conus textile, slows voltage-gated sodium (Na(V)) channel inactivation in molluscan neurons, but its mammalian ion channel targets remain undetermined. In this study, we confirmed that TxVIA was in...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7401249/ https://www.ncbi.nlm.nih.gov/pubmed/32629781 http://dx.doi.org/10.3390/md18070343 |
Sumario: | The 27-amino acid (aa)-long δ-conotoxin TxVIA, originally isolated from the mollusc-hunting cone snail Conus textile, slows voltage-gated sodium (Na(V)) channel inactivation in molluscan neurons, but its mammalian ion channel targets remain undetermined. In this study, we confirmed that TxVIA was inactive on mammalian Na(V)1.2 and Na(V)1.7 even at high concentrations (10 µM). Given the fact that invertebrate Na(V) channel and T-type calcium channels (Ca(V)3.x) are evolutionarily related, we examined the possibility that TxVIA may act on Ca(V)3.x. Electrophysiological characterisation of the native TxVIA on Ca(V)3.1, 3.2 and 3.3 revealed that TxVIA preferentially inhibits Ca(V)3.2 current (IC(50) = 0.24 μM) and enhances Ca(V)3.1 current at higher concentrations. In fish bioassays TxVIA showed little effect on zebrafish behaviours when injected intramuscular at 250 ng/100 mg fish. The binding sites for TxVIA at Na(V)1.7 and Ca(V)3.1 revealed that their channel binding sites contained a common epitope. |
---|