Pollock B J, McKenzie A S, Kemp B E, McPhee D A, D'Apice A J
Department of Nephrology, Royal Melbourne Hospital, Victoria, Australia.
Clin Exp Immunol. 1989 Dec;78(3):323-8.
Human monoclonal antibodies were raised by in vitro immunization of normal human spleen cells with denatured HIV-1 and subsequent fusion to an Epstein-Barr virus (EBV) transformed cell line. Three monoclonals reacted with both gag-encoded p24 core protein and env-encoded gp41 transmembrane glycoprotein. The cross-reaction was confirmed by reactivity with p24- and gp41-derived recombinant peptides. The peptides share two amino acid sequences which may be the basis for the cross-reaction. Attempted epitope mapping using synthetic peptides was unsuccessful due to non-specific reactivity with the short linear peptides.
通过用变性的HIV-1对正常人脾细胞进行体外免疫,随后与爱泼斯坦-巴尔病毒(EBV)转化的细胞系融合,制备了人单克隆抗体。三种单克隆抗体与gag编码的p24核心蛋白和env编码的gp41跨膜糖蛋白均发生反应。与p24和gp41衍生的重组肽的反应证实了这种交叉反应。这些肽共有两个氨基酸序列,这可能是交叉反应的基础。由于与短线性肽的非特异性反应,使用合成肽进行表位定位的尝试未成功。