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金刚烷胺特异性抗流感作用的分子基础。

The molecular basis of the specific anti-influenza action of amantadine.

作者信息

Hay A J, Wolstenholme A J, Skehel J J, Smith M H

出版信息

EMBO J. 1985 Nov;4(11):3021-4. doi: 10.1002/j.1460-2075.1985.tb04038.x.

Abstract

Amantadine (1-aminoadamantane hydrochloride) is effective in the prophylaxis and treatment of influenza A infections. In tissue culture this selective, strain-specific antiviral activity occurs at relatively low concentrations (5 microM or less), which inhibit either the initiation of infection or virus assembly. The data reported here demonstrate that the basis of these actions is similar and resides in the virus-coded M2 membrane protein, the product of a spliced transcript of RNA segment 7. Mutations which confer resistance to amantadine are restricted to four amino acids within a hydrophobic sequence, indicating that the drug is targetted against the putative membrane-associated portion of the molecule. The influence of the virus haemagglutinin on the amantadine sensitivity of virus strains implies that the drug may interfere with interactions between these two virus proteins.

摘要

金刚烷胺(盐酸1-金刚烷胺)对甲型流感感染的预防和治疗有效。在组织培养中,这种具有选择性、毒株特异性的抗病毒活性在相对较低浓度(5微摩尔或更低)时出现,可抑制感染的起始或病毒组装。此处报告的数据表明,这些作用的基础相似,且在于病毒编码的M2膜蛋白,它是RNA片段7剪接转录本的产物。赋予对金刚烷胺耐药性的突变仅限于一个疏水序列内的四个氨基酸,这表明该药物靶向分子假定的膜相关部分。病毒血凝素对病毒株金刚烷胺敏感性的影响意味着该药物可能干扰这两种病毒蛋白之间的相互作用。

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