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BmTx3,一种具有两个假定功能面的蝎毒素,分别对A型钾电流和HERG电流有活性。

BmTx3, a scorpion toxin with two putative functional faces separately active on A-type K+ and HERG currents.

作者信息

Huys Isabelle, Xu Chen-Qi, Wang Cheng-Zhong, Vacher Hélène, Martin-Eauclaire Marie-France, Chi Cheng-Wu, Tytgat Jan

机构信息

Laboratory of Toxicology, University of Leuven, Faculty of Pharmaceutical Sciences, E. Van Evenstraat 4, 3000 Leuven, Belgium.

出版信息

Biochem J. 2004 Mar 15;378(Pt 3):745-52. doi: 10.1042/BJ20031324.

Abstract

A novel HERG channel blocker was isolated from the venom of the scorpion Buthus martensi Karsch, sequenced and characterized at the pharmacological level after chemical synthesis. According to the determined amino acid sequence, the cDNA and genomic genes were then cloned. The genomic gene consists of two exons interrupted by an intron of 65 bp at position -6 upstream from the mature toxin. The protein sequence of this toxin was completely identical with that of a known A-type K+ current blocker BmTx3, belonging to scorpion alpha-KTx subfamily 15. Thus BmTx3 is the first reported alpha-KTx peptide also showing HERG-blocking activity, like gamma-KTx peptides. Moreover, different from classical alpha-KTx peptides, such as charybdotoxin, BmTx3 cannot block Shaker -type K+ channels. Phylogenetic tree analysis reveals that this toxin takes an intermediate position between classical alpha-KTx and gamma-KTx toxins. From a structural point of view, we propose that two separate functional faces might exist on the BmTx3 molecule, responsible for the two different K+-current-blocking functions. Face A, composed of Arg18 and Lys19 in the alpha-helix side, might correspond to HERG blocking activity, whereas Face B, containing a putative functional dyad (Lys27 and Tyr36) in the beta-sheet side, might correspond to A-type blocking activity. A specific deletion mutant with the disrupted Face B, BmTx3-Y36P37del, loses the A-type current-blocking activity, but keeps a similar HERG-blocking activity, as seen with the wild-type toxin.

摘要

从东亚钳蝎毒液中分离出一种新型HERG通道阻滞剂,经化学合成后进行测序并在药理学水平上进行表征。根据测定的氨基酸序列,随后克隆了cDNA和基因组基因。基因组基因由两个外显子组成,在成熟毒素上游-6位处有一个65 bp的内含子将其打断。该毒素的蛋白质序列与已知的A型钾电流阻滞剂BmTx3完全相同,属于蝎α-KTx亚家族15。因此,BmTx3是首个被报道的也具有HERG阻断活性的α-KTx肽,类似于γ-KTx肽。此外,与经典的α-KTx肽(如蝎毒素)不同,BmTx3不能阻断Shaker型钾通道。系统发育树分析表明,该毒素在经典α-KTx和γ-KTx毒素之间处于中间位置。从结构角度来看,我们提出BmTx3分子上可能存在两个独立的功能面,分别负责两种不同的钾电流阻断功能。面A由α-螺旋侧的Arg18和Lys19组成,可能对应HERG阻断活性,而面B在β-折叠侧含有一个假定的功能二元组(Lys27和Tyr36),可能对应A型阻断活性。一个面B被破坏的特异性缺失突变体BmTx3-Y36P37del失去了A型电流阻断活性,但与野生型毒素一样保留了类似的HERG阻断活性。

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