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[金刚乙胺和金刚烷胺对流感病毒蛋白与模型脂质膜相互作用的影响]

[Effect of remantadine and amantadine on the interaction of influenza virus proteins with model lipid membranes].

作者信息

Kharitonenkov I G, El Karadaghi S, Fedorov A N, Zakomyrdin Iu A, Tverdislov V A

出版信息

Vopr Virusol. 1988 Jan-Feb;33(1):22-6.

PMID:3369145
Abstract

The influence of adamantane derivatives (remantadine and amantadine) on the surface charge of lipid bilayer when they are adsorbed on an artificially formed bilayer lipid membrane (BLM) was studied. The presence of the final number of binding centres on the BLM surface for remantadine and amantadine molecules and the cooperative nature of interaction of these compounds with the lipid bilayer were demonstrated. The features of interaction of influenza virus proteins isolated from the virion--M protein and a mixture of surface glycoproteins--were studied. Both antiviral compounds were shown to reduce markedly M protein adsorption on the lipid bilayer and to affect negligibly the sorption properties of the surface glycoproteins. Remantadine molecules interact directly with M protein molecules reducing their hydrophobic properties and, thereby, reducing the affinity of this viral polypeptide to lipid bilayer.

摘要

研究了金刚烷衍生物(金刚乙胺和金刚烷胺)吸附在人工形成的双层脂质膜(BLM)上时对脂质双层表面电荷的影响。证明了BLM表面存在金刚乙胺和金刚烷胺分子的最终结合中心数量,以及这些化合物与脂质双层相互作用的协同性质。研究了从病毒粒子中分离出的流感病毒蛋白——M蛋白和表面糖蛋白混合物的相互作用特征。结果表明,这两种抗病毒化合物均能显著降低M蛋白在脂质双层上的吸附,而对表面糖蛋白的吸附特性影响可忽略不计。金刚乙胺分子直接与M蛋白分子相互作用,降低其疏水特性,从而降低这种病毒多肽对脂质双层的亲和力。

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