首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Purification and pharmacological characterization of BmKK2 (alpha-KTx 14.2), a novel potassium channel-blocking peptide, from the venom of Asian scorpion Buthus martensi Karsch
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Purification and pharmacological characterization of BmKK2 (alpha-KTx 14.2), a novel potassium channel-blocking peptide, from the venom of Asian scorpion Buthus martensi Karsch

机译:来自亚洲蝎子Buthus martensi Karsch毒液的新型钾通道阻断肽BmKK2(alpha-KTx 14.2)的纯化和药理学表征

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摘要

BmKK2 (alpha-KTx 14.2) is one of the novel short-chain peptides found in molecular cloning of a venom gland cDNA library from Asian scorpion Buthus martensi Karsch. Based upon its amino acid sequence, the peptide was proposed to adopt a classical alpha/beta-scaffold for alpha-KTxs. In the present study, we purified BmKK2 from the venom of B. martensi Karsch, and investigated its action on voltage-dependent K+ currents in dissociated hippocampal neurons from neonatal rats. BmKK2 (10-100 muM) selectively inhibited the delayed rectifier K+ current, but did not affect the fast transient K+ current. The inhibition of BmKK2 on the delayed rectifier K+ current was reversible and voltage-independent. The peptide did not affect the steady-state activation of the current, but caused a depolarizing shift (about 9 mV) of its steady-state inactivation curve. The results demonstrate that BmKK2 is a novel K+ channel-blocking scorpion peptide.
机译:BmKK2(alpha-KTx 14.2)是从亚洲蝎子Buthus martensi Karsch的毒腺cDNA文库的分子克隆中发现的新型短链肽之一。基于其氨基酸序列,该肽被提议采用经典的α/β-支架用于α-KTxs。在本研究中,我们从B. martensi Karsch的毒液中纯化了BmKK2,并研究了其对新生大鼠离体海马神经元中电压依赖性K +电流的作用。 BmKK2(10-100μM)有选择地抑制延迟的整流器K +电流,但不影响快速瞬态K +电流。 BmKK2对延迟整流器K +电流的抑制作用是可逆的,并且与电压无关。该肽不会影响电流的稳态激活,但会导致其稳态灭活曲线发生去极化移位(约9 mV)。结果表明BmKK2是一种新型的K +通道封锁蝎肽。

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