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作 者:杨克俭[1] 阮力[1] 孙朝辉 陆柔剑[1] 朱既明[1]
机构地区:[1]中国预防医学科学院病毒学研究所
出 处:《病毒学报》1997年第1期13-18,共6页Chinese Journal of Virology
摘 要:在利用PCR方法克隆麻疹病毒L4株血凝素(HA)基因的过程中,获得了一个助融合活性丢失的B号克隆。其氨基酸序列与具有助融合活性的A号克隆相比,有4个位点不同,分别位于96、117、148及543位。通过基因间部分序列的交换及定点回复突变,获得了相应位点的突变体。对这些突变体的助融合活性研究发现,117、148及543位氨基酸的改变不影响助融合活性,而当96位脯氨酸定点回复突变为亮氨酸后,B克隆血凝素蛋白获得了助融合活性。提示HA蛋白96位氨基酸是影响助融合活性的一个重要氨基酸。A hemmagglutinin gene HA(B) of measles virus which has lost the function of fusion helper was cloned from L4 strain of measles virus by PCR.Sequence analysis showed that four amino acids were changed at position 96、117、148 and 543 in the clone HA(B) when compared with that of the clone HA(A) which possesses good fusion helper function.A series of mutated HA genes were obtained by exchanging the corresponding fragments of these two different clones and by site-directed mutation.It was found that changes of amino acids at the positions 117、148 and 543 did not affect the fusion helper function,but the fusion helper function of HA(B) gene could be restored when its proline at 96 position was mutated back to leucine.The results indicate that the amino acid located at position 96 of measles virus HA is closely related with its fusion helper function.
分 类 号:R373.11[医药卫生—病原生物学]
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