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蛋白质结构的简并微扰作为麻醉作用的机制。

Degenerate perturbations of protein structure as the mechanism of anaesthetic action.

作者信息

Richards C D, Martin K, Gregory S, Keightley C A, Hesketh T R, Smith G A, Warren G B, Metcalfe J C

出版信息

Nature. 1978;276(5690):775-9. doi: 10.1038/276775a0.

Abstract

The interaction of the n-alkanols with lipid bilayers and excitable membranes shows that there is no simple correlation between conduction block and any of the perturbations of bilayer structure currently proposed as unitary mechanisms of local anaesthetic action. We propose instead that the n-alkanols act by direct interaction with target proteins to cause perturbations which depend directly on the precise structure of the alcohol.

摘要

正链烷醇与脂质双层膜和可兴奋膜的相互作用表明,传导阻滞与目前作为局部麻醉作用单一机制提出的任何双层膜结构扰动之间不存在简单的相关性。相反,我们提出正链烷醇通过与靶蛋白直接相互作用来发挥作用,从而引起直接依赖于醇精确结构的扰动。

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