Stühler A, Wege H, Siddell S G
Institute of Virology and Immunobiology, University of Würzburg, Germany.
J Gen Virol. 1991 Jul;72 ( Pt 7):1655-8. doi: 10.1099/0022-1317-72-7-1655.
A panel of murine hepatitis virus (MHV) surface (S) glycoprotein-specific monoclonal antibodies (MAbs), which recognize either continuous or discontinuous epitopes, were tested in competitive binding assays. The results indicate that the binding site of MAb 30B amino acids 395 to 406 in the amino-terminal S1 subunit, is involved in the discontinuous epitope designated antigenic site A. This site is a major determinant for the induction of neutralizing antibodies. These data define, for the first time, the location of a functionally important domain on the MHV S protein.
一组针对鼠肝炎病毒(MHV)表面(S)糖蛋白的特异性单克隆抗体(MAb),这些抗体识别连续或不连续表位,在竞争性结合试验中进行了检测。结果表明,单克隆抗体30B在氨基末端S1亚基中395至406位氨基酸的结合位点,参与了被称为抗原位点A的不连续表位。该位点是诱导中和抗体的主要决定因素。这些数据首次确定了MHV S蛋白上一个功能重要结构域的位置。