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首页> 外文期刊>Virology Journal >The Severe Acute Respiratory Syndrome (SARS)-coronavirus 3a protein may function as a modulator of the trafficking properties of the spike protein
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The Severe Acute Respiratory Syndrome (SARS)-coronavirus 3a protein may function as a modulator of the trafficking properties of the spike protein

机译:严重急性呼吸系统综合症(SARS)冠状病毒3a蛋白可能起着穗蛋白转运特性的调节作用

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Background A recent publication reported that a tyrosine-dependent sorting signal, present in cytoplasmic tail of the spike protein of most coronaviruses, mediates the intracellular retention of the spike protein. This motif is missing from the spike protein of the severe acute respiratory syndrome-coronavirus (SARS-CoV), resulting in high level of surface expression of the spike protein when it is expressed on its own in vitro. Presentation of the hypothesis It has been shown that the severe acute respiratory syndrome-coronavirus genome contains open reading frames that encode for proteins with no homologue in other coronaviruses. One of them is the 3a protein, which is expressed during infection in vitro and in vivo. The 3a protein, which contains a tyrosine-dependent sorting signal in its cytoplasmic domain, is expressed on the cell surface and can undergo internalization. In addition, 3a can bind to the spike protein and through this interaction, it may be able to cause the spike protein to become internalized, resulting in a decrease in its surface expression. Testing the hypothesis The effects of 3a on the internalization of cell surface spike protein can be examined biochemically and the significance of the interplay between these two viral proteins during viral infection can be studied using reverse genetics methodology. Implication of the hypothesis If this hypothesis is proven, it will indicate that the severe acute respiratory syndrome-coronavirus modulates the surface expression of the spike protein via a different mechanism from other coronaviruses. The interaction between 3a and S, which are expressed from separate subgenomic RNA, would be important for controlling the trafficking properties of S. The cell surface expression of S in infected cells significantly impacts viral assembly, viral spread and viral pathogenesis. Modulation by this unique pathway could confer certain advantages during the replication of the severe acute respiratory syndrome-coronavirus.
机译:背景技术最近的出版物报道存在于大多数冠状病毒的刺突蛋白的细胞质尾中的酪氨酸依赖性分选信号介导了刺突蛋白的细胞内保留。严重急性呼吸系统综合症冠状病毒(SARS-CoV)的刺突蛋白中缺少此基序,导致刺突蛋白在体外单独表达时,其表面表达水平很高。假设的表述已经表明,严重的急性呼吸系统综合症冠状病毒基因组包含开放阅读框,其编码与其他冠状病毒中没有同源性的蛋白质。其中之一是3a蛋白,该蛋白在体外和体内感染过程中表达。 3a蛋白在其胞质结构域中包含酪氨酸依赖性分选信号,该3a蛋白在细胞表面表达并可以内在化。另外,3a可以与刺突蛋白结合,并且通过这种相互作用,它可能能够使刺突蛋白内在化,从而导致其表面表达降低。检验假说可以用化学方法检查3a对细胞表面刺突蛋白内在化的影响,并可以使用反向遗传学方法研究这两种病毒蛋白在病毒感染过程中相互作用的重要性。假设的含义如果该假设得到证实,则表明严重的急性呼吸系统综合症冠状病毒通过与其他冠状病毒不同的机制来调节刺突蛋白的表面表达。从单独的亚基因组RNA表达的3a和S之间的相互作用对于控制S的运输特性非常重要。被感染细胞中S的细胞表面表达显着影响病毒装配,病毒传播和病毒发病机理。通过这种独特的途径进行调节可在重症急性呼吸综合征-冠状病毒的复制过程中赋予某些优势。

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  • 来源
    《Virology Journal》 |2005年第1期|共页
  • 作者

    Yee-Joo Tan;

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