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Mapping of an Antigenic Site on the Nucleocapsid Protein of Human Parainfluenza Virus Type 3

机译:人类副流感病毒3型核衣壳蛋白上的抗原性位点图谱

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Human parainfluenza virus type 3 (hPIV3) is a respiratory tract pathogen. The current study aimed to investigate immunodominant regions of hPIV3 nucleocapsid (N) protein by using monoclonal antibodies (mAbs) raised against recombinant N protein and human serum specimens from hPIV3-infected individuals. A panel of murine mAbs was generated following immunization with yeast-expressed hPIV3 N protein self-assembled to nucleocapsid-like particles. All mAbs recognized native viral nucleocapsids in hPIV3-infected cells as confirmed by an indirect immunofluorescence analysis. Antigenic sites recognized by the mAbs were mapped using recombinant overlapping N protein fragments. One major immunodominant site was identified in the carboxy-terminal region (amino acids [aa] 397–486) of hPIV3 N protein. Further analysis with smaller N protein fragments and a synthetic peptide revealed one linear epitope representing aa 437–446 of the N protein located within this antigenic site. This epitope was reactive with 46% of hPIV3 IgG-positive sera. These results suggest that the above antigenic site on the N protein is important in eliciting a humoral immune response against hPIV3.
机译:3型人类副流感病毒(hPIV3)是呼吸道病原体。当前的研究旨在通过使用针对重组N蛋白的单克隆抗体(mAb)和来自hPIV3感染者的人血清标本来研究hPIV3核衣壳(N)蛋白的免疫优势区域。用自组装成核衣壳样颗粒的酵母表达的hPIV3 N蛋白免疫后,产生一组鼠单克隆抗体。通过间接免疫荧光分析证实,所有mAb均可识别hPIV3感染的细胞中的天然病毒核衣壳。使用重组重叠的N蛋白片段对mAb识别的抗原位点进行定位。在hPIV3 N蛋白的羧基末端区域(氨基酸[aa] 397–486)鉴定出一个主要的免疫优势位点。用较小的N蛋白片段和合成肽进行的进一步分析显示,一个线性表位代表位于该抗原位点的N蛋白的437–446位氨基酸。该表位与46%的hPIV3 IgG阳性血清反应。这些结果表明,N蛋白上的上述抗原位点在引发针对hPIV3的体液免疫应答中很重要。

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  • 来源
    《Viral Immunology 》 |2009年第3期| 181-188| 共8页
  • 作者单位

    Laboratory of Immunology and Cell Biology, Institute of Biotechnology, Vilnius, Lithuania.;

    Laboratory of Immunology and Cell Biology, Institute of Biotechnology, Vilnius, Lithuania.;

    Laboratory of Immunology and Cell Biology, Institute of Biotechnology, Vilnius, Lithuania.;

    Laboratory of Immunology and Cell Biology, Institute of Biotechnology, Vilnius, Lithuania.;

    Laboratory of Eukaryote Gene Engineering, Institute of Biotechnology, Vilnius, Lithuania.;

    Laboratory of Eukaryote Gene Engineering, Institute of Biotechnology, Vilnius, Lithuania.;

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