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Characterisation of δ-Conotoxin TxVIA as a Mammalian T-Type Calcium Channel Modulator

机译:δ-芋螺毒素Txvia作为哺乳动物T型钙通道调制器的表征

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摘要

The 27-amino acid (aa)-long δ-conotoxin TxVIA, originally isolated from the mollusc-hunting cone snail , slows voltage-gated sodium (Na ) 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 1.2 and Na 1.7 even at high concentrations (10 µM). Given the fact that invertebrate Na channel and T-type calcium channels (Ca 3.x) are evolutionarily related, we examined the possibility that TxVIA may act on Ca 3.x. Electrophysiological characterisation of the native TxVIA on Ca 3.1, 3.2 and 3.3 revealed that TxVIA preferentially inhibits Ca 3.2 current (IC = 0.24 μM) and enhances Ca 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 1.7 and Ca 3.1 revealed that their channel binding sites contained a common epitope.
机译:最初从软体动物狩猎锥蜗牛分离出27-氨基酸(AA)-Longδ-芋头毒素TXVIA减缓了软体动物中的电压门控钠(NA)通道灭活,但其哺乳动物离子通道靶仍未确定。在这项研究中,我们证实Txvia甚至在高浓度(10μm)上即使在哺乳动物Na 1.2和Na 1.7上无活性。鉴于无脊椎动物Na通道和T型钙通道(CA 3.x)进化相关的事实,我们检查了TXVIA可能对CA 3.x作用的可能性。 CA 3.1,3.2和3.3上天然TXVIA的电生理学特征揭示了TXVIA优先抑制CA 3.2电流(IC =0.24μm)并以较高浓度的增强CA 3.1电流。在鱼生物测定中,TXvia在注射250 ng / 100毫克鱼的肌肉内时对斑马鱼行为效果很小。在Na 1.7和Ca 3.1的Txvia的结合位点显示其通道结合位点含有常见表位。

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