Cooper J A, Cooper L T, Saul A J
Queensland Institute of Medical Research, Brisbane, Australia.
Mol Biochem Parasitol. 1992 Apr;51(2):301-12. doi: 10.1016/0166-6851(92)90080-4.
The locations of the epitopes of a panel of mouse monoclonal antibodies directed against the Plasmodium falciparum merozoite surface antigen MSA 1 were mapped by using naturally occurring processed fragments, by chemical cleavage of the protein and by comparison of the isolate-specificity of binding with known sequence variation. By these criteria, the most antigenic region occurs in the cysteine-rich, invariant 19-kDa carboxyl terminal domain with 12/19 monoclonal antibodies (mAbs) binding to this region. One of these mAbs recognized an epitope near the C-terminal putative glycosylphosphatidylinositol anchor site. This was the only mAb which significantly inhibited parasite growth in vitro. The other mAbs recognized conformational epitopes involving the cysteine residues located throughout this fragment. This study has identified further naturally occurring processing sites and a consensus processing site sequence is now emerging.
利用天然存在的加工片段、蛋白质的化学裂解以及结合的分离株特异性与已知序列变异的比较,绘制了一组针对恶性疟原虫裂殖子表面抗原MSA 1的小鼠单克隆抗体的表位定位图。根据这些标准,最具抗原性的区域出现在富含半胱氨酸的、恒定的19 kDa羧基末端结构域,19种单克隆抗体中有12种与该区域结合。其中一种单克隆抗体识别靠近C末端假定糖基磷脂酰肌醇锚定位点的表位。这是唯一一种在体外显著抑制寄生虫生长的单克隆抗体。其他单克隆抗体识别涉及该片段中各处半胱氨酸残基的构象表位。本研究确定了更多天然存在的加工位点,现在正在形成一个共有加工位点序列。