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神经毒性流感病毒株神经氨酸酶的变化。

Changes in the neuraminidase of neurovirulent influenza virus strains.

作者信息

Ward A C

机构信息

Biomolecular Research Institute, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Virus Genes. 1995;10(3):253-60. doi: 10.1007/BF01701815.

Abstract

The influenza virus A/WS/33 has been adapted to mouse brain to produce two neurovirulent derivatives, A/NWS/33 (NWS) and A/WSN/33 (WSN), with the viral neuraminidase gene shown to be the major determinant of neurovirulence. The complete nucleotide sequence of the NA genes from each strain has been determined, which has allowed the identification of changes that have occurred during adaptation to mouse brain. Five changes are shared by the neurovirulent strains. Comparison to the known neuraminidase structure has identified four of these that may affect the active site of the enzyme. In addition, significant differences in the properties of the neuraminidase from the neurovirulent strains were observed relative to the parent strain. While no correlation was observed between neurovirulence and overall neuraminidase activity or preference for a particular N-substitution, the enzymes from both neurovirulent strains showed an increased preference for small substrates and those with 2-->3 linkages, and their activity was potentiated by Ca2+ ions.

摘要

甲型流感病毒A/WS/33已适应小鼠脑,产生了两种具有神经毒力的衍生物,即A/NWS/33(NWS)和A/WSN/33(WSN),病毒神经氨酸酶基因被证明是神经毒力的主要决定因素。已确定每个毒株NA基因的完整核苷酸序列,这使得能够鉴定在适应小鼠脑过程中发生的变化。两种具有神经毒力的毒株共有五个变化。与已知的神经氨酸酶结构进行比较后,已确定其中四个变化可能会影响该酶的活性位点。此外,相对于亲本毒株,观察到具有神经毒力的毒株的神经氨酸酶特性存在显著差异。虽然未观察到神经毒力与总体神经氨酸酶活性或对特定N取代的偏好之间存在相关性,但两种具有神经毒力的毒株的酶对小分子底物和具有2→3连接的底物表现出更高的偏好,并且它们的活性被Ca2+离子增强。

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