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首页> 外文期刊>Journal of Medical Virology >Identification of epitopes in the nucleocapsid protein of Nipah virus using a linear phage-displayed random peptide library.
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Identification of epitopes in the nucleocapsid protein of Nipah virus using a linear phage-displayed random peptide library.

机译:使用线性噬菌体展示的随机肽库鉴定尼帕病毒核衣壳蛋白中的表位。

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摘要

A random peptide library of heptamers displayed on the surface of M13 bacteriophage was used to identify specific epitopes of antibodies in pooled sera of swine naturally infected by Nipah virus. The selected heptapeptides were aligned with protein sequences of Nipah virus and several putative epitopes were identified within the nucleocapsid protein. A total of 41 of 60 (68%) selected phage clones had inserts resembling a region with the sequence SNRTQGE, located at the C-terminal end (amino acids 503-509) of the nucleocapsid protein. The binding of antibodies in the swine and human antisera to the phage clone was inhibited by a synthetic peptide corresponding to this region. Epitopes identified by phage display are consistent with the predicted antigenic sites for the Nipah virus nucleocapsid protein. The selected phage clone used as a coating antigen discriminated swine and human Nipah virus sera-positive from sera-negative samples exhibiting characteristics, which might be attractive for diagnostic tests.
机译:M13噬菌体表面上显示的七聚体随机肽库用于鉴定天然被尼帕病毒感染的猪血清中抗体的特异性表位。将选定的七肽与尼帕病毒的蛋白序列进行比对,并在核衣壳蛋白中鉴定出几个推定的表位。在60个选定的噬菌体克隆中,共有41个(68%)具有类似SNRTQGE序列的插入片段,位于核苷酸衣壳蛋白的C末端(氨基酸503-509)。猪和人抗血清中抗体与噬菌体克隆的结合被对应于该区域的合成肽抑制。通过噬菌体展示鉴定的表位与尼帕病毒核衣壳蛋白的预测抗原位点一致。选定的噬菌体克隆用作包被抗原,从表现出特征的血清阴性样品中区分出猪和人Nipah病毒的血清阳性,这可能对诊断测试具有吸引力。

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