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Spike protein homology between the SARS-associated virus and murine hepatitis virus implies existence of a putative receptor-binding region

机译:SARS相关病毒和鼠肝炎病毒之间的穗蛋白同源性暗示存在假定的受体结合区

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Coronavirus has been determined to be the cause of the recent outbreak of severe acute respiratory syndrome (SARS). Human coronavirus 229E had been studied well and its receptor-binding domain was restricted to aa417 -547 of S protein. However, this region has no homology with the newly separated SARS-associated virus (Hong Kong isolate CUHK-W1). Then we analyzed the phylogenesis of S1 subunit of the coronavirus spike protein (SARS-associated virus, Hong Kong isolate CUHK-W1). Interestingly, the highest homology between murine hepatitis virus (MHV) and SARS-associated coronavirus was found. And the important sites (aa62-65 and aa214-216) on the spike protein of MHV with receptor-binding capacity were highly conservative in comparison with the newly separated SARS-associated virus (the corresponding sites are aa51-54 and aa195 -197). These results from bioinformatics analysis might help us to study the receptor-binding sites of SARS-associated virus and the mechanism of the virus entry into the target cell, and design antiviral drugs and potent vaccines.
机译:已确定冠状病毒是近期爆发的严重急性呼吸道综合症(SARS)的原因。人类冠状病毒229E已被很好地研究,其受体结合域仅限于S蛋白的aa417 -547。但是,该区域与新分离出的SARS相关病毒(香港分离株CUHK-W1)没有同源性。然后,我们分析了冠状病毒刺突蛋白(SARS相关病毒,香港分离株CUHK-W1)的S1亚基的系统发育。有趣的是,鼠肝炎病毒(MHV)与SARS相关冠状病毒之间的同源性最高。与新分离的SARS相关病毒相比,MHV穗蛋白上具有受体结合能力的重要位点(aa62-65和aa214-216)高度保守(相应位点为aa51-54和aa195 -197)。 。生物信息学分析的这些结果可能有助于我们研究SARS相关病毒的受体结合位点以及该病毒进入靶细胞的机制,并设计抗病毒药物和有效疫苗。

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