首页> 外文期刊>Molecular pharmacology. >A novel family of insect-selective peptide neurotoxins targeting insect large-conductance calcium-activated K+ channels isolated from the venom of the theraphosid spider Eucratoscelus constrictus.
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A novel family of insect-selective peptide neurotoxins targeting insect large-conductance calcium-activated K+ channels isolated from the venom of the theraphosid spider Eucratoscelus constrictus.

机译:一个新的昆虫选择性肽神经毒素家族,针对昆虫的大电导钙激活的K +通道,该通道从节肢动物蜘蛛Eucratoscelus constrictus的毒液中分离。

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摘要

Spider venoms are actively being investigated as sources of novel insecticidal agents for biopesticide engineering. After screening 37 theraphosid spider venoms, a family of three new "short-loop" inhibitory cystine knot insecticidal toxins (kappa-TRTX-Ec2a, kappa-TRTX-Ec2b, and kappa-TRTX-Ec2c) were isolated and characterized from the venom of the African tarantula Eucratoscelus constrictus. Whole-cell patch-clamp recordings from cockroach dorsal unpaired median neurons revealed that, despite significant sequence homology with other theraphosid toxins, these 29-residue peptides lacked activity on insect voltage-activated sodium and calcium channels. It is noteworthy that kappa-TRTX-Ec2 toxins were all found to be high-affinity blockers of insect large-conductance calcium-activated K(+) (BK(Ca)) channel currents with IC(50) values of 3 to 25 nM. In addition, kappa-TRTX-Ec2a caused the inhibition of insect delayed-rectifier K(+) currents, but only at significantly higher concentrations. kappa-TRTX-Ec2a and kappa-TRTX-Ec2b demonstrated insect-selective effects, whereas the homologous kappa-TRTX-Ec2c also resulted in neurotoxic signs in mice when injected intracerebroventricularly. Unlike other theraphosid toxins, kappa-TRTX-Ec2 toxins induce a voltage-independent channel block, and therefore, we propose that these toxins interact with the turret and/or loop region of the external entrance to the channel and do not project deeply into the pore of the channel. Furthermore, kappa-TRTX-Ec2a and kappa-TRTX-Ec2b differ from other theraphotoxins at the C terminus and positions 5 to 6, suggesting that these regions of the peptide contribute to the phyla selectivity and are involved in targeting BK(Ca) channels. This study therefore establishes these toxins as tools for studying the role of BK(Ca) channels in insects and lead compounds for the development of novel insecticides.
机译:蜘蛛毒被积极研究作为生物农药工程学中新型杀虫剂的来源。在筛选了37种节肢动物蜘蛛毒液后,从蛇毒的毒液中分离并鉴定了三个新的“短环”抑制性胱氨酸结杀虫毒素(kappa-TRTX-Ec2a,kappa-TRTX-Ec2b和kappa-TRTX-Ec2c)家族。非洲的狼蛛Eucratoscelus constrictus。蟑螂背侧未配对正中神经元的全细胞膜片钳记录显示,尽管与其他节肢动物毒素具有显着的序列同源性,但是这29个残基肽对昆虫电压激活的钠和钙通道缺乏活性。值得注意的是,所有kappa-TRTX-Ec2毒素都被发现是昆虫大电导钙激活的K(+)(BK(Ca))通道电流的高亲和力阻滞剂,IC(50)值为3至25 nM 。此外,kappa-TRTX-Ec2a引起昆虫延迟整流器K(+)电流的抑制,但仅在明显更高的浓度下。 kappa-TRTX-Ec2a和kappa-TRTX-Ec2b表现出昆虫选择性作用,而同源的kappa-TRTX-Ec2c在脑室内注射时也可引起小鼠神经毒性。与其他节肢动物毒素不同,kappa-TRTX-Ec2毒素会诱导电压依赖性通道阻滞,因此,我们建议这些毒素与通道外部入口的炮塔和/或环路区域相互作用,并且不会深入到通道外通道的孔。此外,kappa-TRTX-Ec2a和kappa-TRTX-Ec2b在C末端和位置5至6与其他theraphotoxins不同,这表明该肽段的这些区域有助于系统选择性,并参与靶向BK(Ca)通道。因此,这项研究将这些毒素确立为研究昆虫中BK(Ca)通道和开发新型杀虫剂的先导化合物的作用的工具。

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