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[中国分离的B亚组呼吸道合胞病毒株G蛋白基因cDNA的克隆与测序]

[Cloning and sequencing of cDNA from G protein gene of subgroup B respiratory syncytial virus strain isolated in China].

作者信息

Geng X, Wang Z, Qian Y, Zhu R, Deng J

机构信息

Beijing Municipal Laboratory of Infection and Immunity, Capital Institute of Pediatrics, Beijing 100020.

出版信息

Wei Sheng Wu Xue Bao. 1999 Feb;39(1):23-8.

Abstract

The nucleotide sequence of the G protein gene of respiratory syncytial virus (RSV) CC169 strain isolated from China that has been identified as subgroup B with monoclonal antibodies, was determined from cDNA that had been amplified by RT-PCR and cloned into pTZ18R plasmid vector. The homology of nucleotide was 94% as compared with G protein cDNA of a RSV prototype strain (CH18537). Deduced amino acid identity of G protein was 89.4%. The amino acid changes were only in the extracellular part of the protein where there were two extensive divergent domains with a highly conserved region in between; whereas the cytoplasmic and transmembrane domains were conserved. This study demonstrates the sequence diversity of the G protein of subgroup B RSV between a Chinese isolate and the prototype strain CH18537.

摘要

从中国分离出的呼吸道合胞病毒(RSV)CC169株,已通过单克隆抗体鉴定为B亚组,其G蛋白基因的核苷酸序列是从经逆转录聚合酶链反应(RT-PCR)扩增并克隆到pTZ18R质粒载体的互补DNA(cDNA)中确定的。与RSV原型株(CH18537)的G蛋白cDNA相比,核苷酸同源性为94%。推导的G蛋白氨基酸同一性为89.4%。氨基酸变化仅发生在蛋白质的细胞外部分,该部分有两个广泛的差异结构域,中间有一个高度保守的区域;而细胞质和跨膜结构域是保守的。本研究证明了中国分离株与原型株CH18537之间B亚组RSV G蛋白的序列多样性。

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