首页> 外文期刊>Journal of Equine Science >Identification of the Major Epitope in the GL Protein of Equine Arteritis Virus (EAV) Recognized by Antibody in EAV-infected Horses Using Synthetic Peptides
【24h】

Identification of the Major Epitope in the GL Protein of Equine Arteritis Virus (EAV) Recognized by Antibody in EAV-infected Horses Using Synthetic Peptides

机译:用合成肽鉴定抗体识别的EAV感染马匹马动脉炎病毒(EAV)G L 蛋白中的主要表位

获取原文
           

摘要

A panel of overlapping peptides covering the ectodomain of the GL protein of equine arteritis virus (EAV) was synthesized to identify the major epitope recognized by the EAV-seropositive horse sera by using enzyme-linked immunosorbent assay (ELISA). Three consecutive peptides, G15 (amino acid residues 75-90), G16 (79-94) and G17 (83-98), strongly reacted with 3 experimentally EAV-infected horse sera. G16 peptide was highly antigenic with all 8 EAV-infected horse sera tested. The ELISA absorbance values and the virus neutralization titers of antibodies in sera periodically collected from EAV-infected horses showed similar patterns. These results indicated that the major linear epitope of the EAV GL protein which was recognized with EAV-infected horse sera was mapped to residues from 83 to 90.
机译:合成了一组覆盖马动脉炎病毒(EAV)G L 蛋白胞外域的重叠肽段,以通过酶联免疫吸附测定法鉴定EAV阳性马血清识别的主要表位( ELISA)。三个连续的肽G15(氨基酸残基75-90),G16(79-94)和G17(83-98)与3种经EAV感染的马血清强烈反应。 G16肽对所有8种被EAV感染的马血清都具有高度抗原性。从被EAV感染的马中定期收集的血清中的抗体ELISA吸光度值和病毒中和滴度显示出相似的模式。这些结果表明,被EAV感染的马血清识别的EAV G L 蛋白的主要线性表位被定位到83至90的残基上。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号