首页> 外文期刊>Peptides: An International Journal >Molecular cloning and electrophysiological studies on the first K(+) channel toxin (LmKTx8) derived from scorpion Lychas mucronatus.
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Molecular cloning and electrophysiological studies on the first K(+) channel toxin (LmKTx8) derived from scorpion Lychas mucronatus.

机译:对蝎子Lychas mucronatus的第一个K(+)通道毒素(LmKTx8)的分子克隆和电生理研究。

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摘要

LmKTx8, the first toxic gene isolated from the venom of scorpion Lychas mucronatus by constructing cDNA library method, was expressed and characterized physiologically. The mature peptide has 40 residues including six conserved cysteines, and is classified as one of alpha-KTx11 subfamily. Using patch-clamp recording, the recombinant LmKTx8 (rLmKTx8) was used to test the effect on voltage-gated K(+) channels (Kv1.3) stably expressed in COS7 cells and large conductance-Ca(2+)-activated K(+) (BK) channels expressed in HEK293. The results of electrophysiological experiments showed that the rLmKTx8 was a potent inhibitor of Kv1.3 channels with an IC(50)=26.40+/-1.62nM, but 100nM rLmKTx8 did not block the BK currents. LmKTx8 or its analogs might serve as a potential candidate for the development of new drugs for autoimmune diseases.
机译:利用构建的cDNA文库方法,从蝎蝎Lychas mucronatus的毒液中分离出了第一个有毒基因LmKTx8,并进行了生理学表征。成熟的肽具有40个残基,包括6个保守的半胱氨酸,被分类为α-KTx11亚家族之一。使用膜片钳记录,重组LmKTx8(rLmKTx8)用于测试对在COS7细胞中稳定表达的电压门控K(+)通道(Kv1.3)和大电导-Ca(2+)激活的K( +)(BK)通道,以HEK293表示。电生理实验结果表明,rLmKTx8是Kv1.3通道的有效抑制剂,IC(50)= 26.40 +/- 1.62nM,但100nM rLmKTx8不会阻断BK电流。 LmKTx8或其类似物可能会成为开发自身免疫性疾病新药的潜在候选者。

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