Sadak A, Taghy Z, Fortier B, Dubremetz J F
Unité 42 INSERM, Villeneuve d'Ascq, France.
Mol Biochem Parasitol. 1988 Jun;29(2-3):203-11. doi: 10.1016/0166-6851(88)90075-8.
A monoclonal antibody (McAb 4A7) raised against a rhoptry enriched subcellular fraction of Toxoplasma gondii tachyzoites reacted in immunofluorescence studies with rod-like organelles located in the anterior part of the organisms and gave specific labeling of rhoptries in immunoelectron microscopy. On immunoblots, two major proteins of 55 and 60 kDa were identified by McAb 4A7. Similar results were obtained both by immunodetection and immunoblotting with tachyzoites, bradyzoites and sporozoites. Pulse chase analysis of [35S]methionine labeled tachyzoites demonstrated that the 55 and 60 kDa rhoptry proteins derived from a 66-68 kDa doublet which was processed approximately 30 min after biosynthesis. Two other monoclonal antibodies (McAb 2F8, McAb 2H3) respectively specific for rhoptry proteins of 55 kDa having a 66 kDa precursor and 60 kDa having a 68 kDa precursor were also obtained; we suggest that they recognize separately the two components of the 55-60 kDa rhoptry protein family of Toxoplasma.
一种针对刚地弓形虫速殖子富含棒状体的亚细胞组分产生的单克隆抗体(McAb 4A7),在免疫荧光研究中与位于虫体前部的棒状细胞器发生反应,并在免疫电子显微镜下对棒状体进行特异性标记。在免疫印迹中,McAb 4A7鉴定出两种主要蛋白质,分子量分别为55 kDa和60 kDa。用速殖子、缓殖子和子孢子进行免疫检测和免疫印迹均得到类似结果。对[35S]甲硫氨酸标记的速殖子进行脉冲追踪分析表明,55 kDa和60 kDa的棒状体蛋白源自一个66 - 68 kDa的双峰,该双峰在生物合成后约30分钟进行加工。还获得了另外两种单克隆抗体(McAb 2F8、McAb 2H3),它们分别对具有66 kDa前体的55 kDa棒状体蛋白和具有68 kDa前体的60 kDa棒状体蛋白具有特异性;我们认为它们分别识别弓形虫55 - 60 kDa棒状体蛋白家族的两个组分。