State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, People's Republic of China.
Peptides. 2012 Jul;36(1):94-9. doi: 10.1016/j.peptides.2012.04.023. Epub 2012 May 8.
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.
蝎毒素是发现新型离子通道调节剂和药物候选物的宝贵资源。钾通道 Kv1.3 是 T 细胞介导的自身免疫性疾病的重要药理学靶点,这促使人们筛选和设计针对 Kv1.3 通道的特异性肽类阻滞剂。Ctri9577 是从蝎子 Chaerilus tricostatus 的毒液中通过构建 cDNA 文库克隆得到的第一个 Chaerilidae 家族的神经毒素基因。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 亚家族的一个新成员。通过表达和纯化技术,获得了重组肽。随后的电生理实验表明,Ctri9577 肽选择性地抑制 Kv1.3 通道电流,IC50 为 0.49±0.45 nM,而对钾通道 Kv1.1、Kv1.2、hERG 和 SK3 没有有效阻断作用。这些发现不仅丰富了 Chaerilidae 家族毒素的知识,还为自身免疫性疾病的治疗提供了一种针对 Kv1.3 通道的新型潜在药物候选物。