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Identification of a new specific Kv1.3 channel blocker, Ctri9577, from the scorpion Chaerilus tricostatus

机译:从蝎子Chaerilus tricostatus鉴定出新的特定Kv1.3通道阻滞剂Ctri9577

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摘要

Scorpion toxins are valuable resources for discovering new ion channel modulators and drug candidates. Potassium channel Kv1.3 is an important pharmacological target of T cell-mediated autoimmune diseases, which are encouraging the screening and design of the specific peptide blockers for Kv1.3 channel. Ctri9577, the first neurotoxin gene of Chaerilidae family was cloned from the venom of the scorpion Chaerilus tricostatus through the constructing its cDNA library. The sequence analysis showed that the mature peptide of Ctri9577 contained 39 amino acid residues including six conserved cysteines, whose low sequence similarity indicated that it was a new member of α-KTx15 subfamily. By using expression and purification technology, the recombinant peptide was obtained. Subsequently, the electrophysiological experiments indicated that the Ctri9577 peptide selectively inhibited Kv1.3 channel current with an IC 50 of 0.49 ± 0.45 nM without effectively blocking potassium channels Kv1.1, Kv1.2, hERG and SK3. All these findings not only enrich the knowledge of toxins from the Chaerilidae family, but also present a novel potential drug candidate targeting Kv1.3 channels for the therapy of autoimmune diseases.
机译:蝎毒素是发现新的离子通道调节剂和候选药物的宝贵资源。钾通道Kv1.3是T细胞介导的自身免疫性疾病的重要药理靶标,正在鼓励筛选和设计Kv1.3通道的特定肽阻滞剂。通过构建其cDNA文库,从蝎形变色龟(Chaerilus tricostatus)的毒液中克隆了变色龙科的第一个神经毒素基因Ctri9577。序列分析表明,Ctri9577的成熟肽含有39个氨基酸残基,包括6个保守的半胱氨酸,其低序列相似性表明它是α-KTx15亚家族的新成员。通过表达和纯化技术,获得了重组肽。随后,电生理实验表明,Ctri9577肽选择性抑制Kv1.3通道电流,IC 50为0.49±0.45 nM,而没有有效地阻断钾通道Kv1.1,Kv1.2,hERG和SK3。所有这些发现不仅丰富了Chaerilidae家族毒素的知识,而且还提出了靶向Kv1.3通道的新型潜在候选药物,可用于治疗自身免疫性疾病。

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