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河豚毒素和石房蛤毒素作用于神经膜钠通道中金属阳离子结合位点的证据。

Evidence that tetrodotoxin and saxitoxin act at a metal cation binding site in the sodium channels of nerve membrane.

作者信息

Henderson R, Ritchie J M, Strichartz G R

出版信息

Proc Natl Acad Sci U S A. 1974 Oct;71(10):3936-40. doi: 10.1073/pnas.71.10.3936.

Abstract

The effects of monovalent, divalent, and trivalent cations on the binding of tetrodotoxin and saxitoxin to intact nerves and to a preparation of solubilized nerve membranes have been examined. All eight divalent and trivalent cations tested, and the monovalent ions Li(+), Tl(+), and H(+) appear to compete reversibly with the toxins for their binding site. The ability of lithium to reduce toxin binding is paralleled by its ability to reduce tetrodotoxin-sensitive ion fluxes through the nerve membrane. We conclude that the toxins act at a metal cation binding site in the sodium channel and suggest that this site is the principal coordination site for cations (normally Na(+) ions) as they pass through the membrane during an action potential. The dissociation constant for Li(+) is 0.1-0.2 M and for Na(+) > 0.6 M, reflecting the weak binding necessary for rapid passage of sodium ions through the channel.

摘要

研究了一价、二价和三价阳离子对河豚毒素和石房蛤毒素与完整神经以及可溶性神经膜制剂结合的影响。所测试的所有八种二价和三价阳离子,以及一价离子Li(+)、Tl(+)和H(+)似乎都能与毒素可逆地竞争其结合位点。锂降低毒素结合的能力与其降低通过神经膜的河豚毒素敏感离子通量的能力相当。我们得出结论,毒素作用于钠通道中的金属阳离子结合位点,并表明该位点是阳离子(通常为Na(+)离子)在动作电位期间穿过膜时的主要配位位点。Li(+)的解离常数为0.1 - 0.2 M,Na(+)的解离常数> 0.6 M,这反映了钠离子快速通过通道所需的弱结合。

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