Kutubuddin M, Gore M M, Banerjee K, Ghosh S N, Kolaskar A S
National Institute of Virology, Pune, India.
Acta Virol. 1993 Dec;37(6):417-28.
Theoretical methods to delineate antibody inducing epitopes have been employed to predict antigenic determinants on envelope glycoprotein (gpE) of Japanese encephalitis (JE), West Nile (WN) and Dengue (DEN) I-IV viruses. A predicted region on JE virus gpE 74CPTTGEAHNEKRAD87 was synthesized, conjugated to KLH (KLH-peptide) and used in immunization of mice. A mouse monoclonal antibody (MoAb IVB4) reactive to the peptide was also found to react with native JE virus gpE. Characterization of the idiotypic (ID) determinants with the help of polyclonal domain-specific anti-ID antibodies revealed that polyclonal anti-KLH-peptide antibodies and MoAb IVB4 are flavivirus-cross-reactive to Hx and NHx domains, respectively. The region 74-87 in JE virus gpE has been mapped as a linking area between Hx and NHx domains. Reactivity of the peptide with sera from JE patients and vaccinees also indicated the feasibility of using predicted peptides for diagnostic and prophylastic purposes.
已采用理论方法来描绘抗体诱导表位,以预测日本脑炎(JE)、西尼罗河(WN)和登革热(DEN)I - IV型病毒包膜糖蛋白(gpE)上的抗原决定簇。合成了JE病毒gpE上预测区域74CPTTGEAHNEKRAD87,将其与钥孔血蓝蛋白偶联(钥孔血蓝蛋白 - 肽),并用于免疫小鼠。还发现一种对该肽有反应的小鼠单克隆抗体(MoAb IVB4)与天然JE病毒gpE发生反应。借助多克隆结构域特异性抗独特型抗体对独特型(ID)决定簇进行表征,结果显示多克隆抗钥孔血蓝蛋白 - 肽抗体和MoAb IVB4分别与黄病毒的Hx和NHx结构域具有交叉反应性。JE病毒gpE中的74 - 87区域已被定位为Hx和NHx结构域之间的连接区域。该肽与JE患者和疫苗接种者血清的反应性也表明使用预测肽用于诊断和预防目的的可行性。