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首页> 外文期刊>Virus Genes >Identification of a Novel B Cell Epitope on the Nucleocapsid Protein of Porcine Reproductive and Respiratory Syndrome Virus by Phage Display.
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Identification of a Novel B Cell Epitope on the Nucleocapsid Protein of Porcine Reproductive and Respiratory Syndrome Virus by Phage Display.

机译:通过噬菌体展示鉴定猪繁殖与呼吸综合征病毒核衣壳蛋白上的新型B细胞表位。

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A phage display peptide library targeting the nucleocapsid (N) protein of porcine reproductive and respiratory syndrome virus (PRRSV) strain CH-1a was generated and used for epitope mapping. After 3 rounds of biopanning with the monoclonal antibody (MAb) N3H2 directed against the N protein, 3 positive phages were screened and sequenced. These phages share a consensus sequence, IQTAFNQGA, which corresponds to the amino acid (AA) 79-87 segment of the CH-1a N protein. A small DNA fragment coding for IQTAFNQGA was expressed as a fusion product, and reacted to N3H2 in Western blots and indirect ELISA. Four truncated peptides (IQTAFNQG, IQTAFNQ, QTAFNQGA, and TAFNQGA) expressed as GST fusion products failed to react with N3H2. The sequences around the N3H2-binding site among the N proteins of 57 PRRSV strains were compared. Our results indicate that the IQTAFNQGA motif is highly conserved among North American and European isolates. We concluded that the precisely defined nona-peptide epitope is a novel conserved Linear B cell epitope on the N protein of PRRSV.
机译:生成了针对猪繁殖与呼吸综合征病毒(PRRSV)株CH-1a的核衣壳(N)蛋白的噬菌体展示肽库,并将其用于表位作图。用针对N蛋白的单克隆抗体(MAb)N3H2进行3轮生物淘选后,筛选并测序了3个阳性噬菌体。这些噬菌体共有一个共有序列IQTAFNQGA,它对应于CH-1a N蛋白的氨基酸(AA)79-87区段。编码IQTAFNQGA的小DNA片段表达为融合产物,并在Western印迹和间接ELISA中与N3H2反应。表示为GST融合产物的四种截短的肽段(IQTAFNQG,IQTAFNQ,QTAFNQGA和TAFNQGA)无法与N3H2反应。比较了57例PRRSV病毒株N蛋白中N3H2结合位点周围的序列。我们的结果表明,IQTAFNQGA基序在北美和欧洲分离株中高度保守。我们得出的结论是,精确定义的九肽表位是PRRSV N蛋白上一个新颖的保守线性B细胞表位。

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