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澳大利亚漏斗网蜘蛛的δ-阿特拉毒素在大鼠脑和昆虫钠通道上与蝎α-毒素结合相互竞争。

Delta-atracotoxins from Australian funnel-web spiders compete with scorpion alpha-toxin binding on both rat brain and insect sodium channels.

作者信息

Little M J, Wilson H, Zappia C, Cestèle S, Tyler M I, Martin-Eauclaire M F, Gordon D, Nicholson G M

机构信息

Department of Health Sciences, University of Technology, Broadway, NSW, Australia.

出版信息

FEBS Lett. 1998 Nov 20;439(3):246-52. doi: 10.1016/s0014-5793(98)01378-7.

Abstract

Atracotoxins are novel peptide toxins from the venom of Australian funnel-web spiders that slow sodium current inactivation in a similar manner to scorpion alpha-toxins. To analyse their interaction with known sodium channel neurotoxin receptor sites we determined their effect on scorpion toxin, batrachotoxin and saxitoxin binding. Nanomolar concentrations of delta-atracotoxin-Hv1 and delta-atracotoxin-Ar1 completely inhibited the binding of the scorpion alpha-toxin AaH II to rat brain synaptosomes as well as the binding of LqhalphaIT, a scorpion alpha-toxin highly active on insects, to cockroach neuronal membranes. Moreover, delta-atracotoxin-Hv1 cooperatively enhanced batrachotoxin binding to rat brain synaptosomes in an analogous fashion to scorpion alpha-toxins. Thus the delta-atracotoxins represent a new class of toxins which bind to both mammalian and insect sodium channels at sites similar to, or partially overlapping with, the receptor binding sites of scorpion alpha-toxins.

摘要

atra毒素是来自澳大利亚漏斗网蜘蛛毒液的新型肽毒素,其以与蝎α毒素类似的方式减缓钠电流失活。为了分析它们与已知钠通道神经毒素受体位点的相互作用,我们确定了它们对蝎毒素、箭毒蛙毒素和石房蛤毒素结合的影响。纳摩尔浓度的δ-atra毒素-Hv1和δ-atra毒素-Ar1完全抑制了蝎α毒素AaH II与大鼠脑突触体的结合,以及对昆虫具有高活性的蝎α毒素LqhalphaIT与蟑螂神经元膜的结合。此外,δ-atra毒素-Hv1以与蝎α毒素类似的方式协同增强箭毒蛙毒素与大鼠脑突触体的结合。因此,δ-atra毒素代表了一类新的毒素,它们在与蝎α毒素受体结合位点相似或部分重叠的位点与哺乳动物和昆虫的钠通道结合。

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