Iwamoto R, Senoh H, Okada Y, Uchida T, Mekada E
Institute of Life Science, Kurume University, Fukuoka, Japan.
J Biol Chem. 1991 Oct 25;266(30):20463-9.
A monoclonal antibody that blocks the binding of diphtheria toxin to Vero cells was isolated by immunizing mice with Vero cell membrane. The antibody inhibits the binding of diphtheria toxin and also CRM197, a mutant form of diphtheria toxin, to Vero cells, and consequently inhibits the cytotoxicity of diphtheria toxin. This antibody does not directly react with the receptor molecule of diphtheria toxin (DTR14.5). Immunoprecipitation and immunoblotting studies revealed that this antibody binds to a novel membrane protein of 27 kDa (DRAP27). When diphtheria toxin receptor was passed through an affinity column made with this antibody, the receptor was trapped only in the presence of DRAP27. These results indicate that DRAP27 and DTR14.5 closely associate in Vero cell membrane and that the inhibition of the binding of diphtheria toxin to the receptor is due to the binding of the antibody to the DRAP27 molecule. Binding studies using 125I-labeled antibody showed that there are many more molecules of DRAP27 on the cell surface than diphtheria toxin-binding sites. However, there is a correlation between the sensitivity of a cell line to diphtheria toxin and the number of DRAP27 molecules on the cell surface, suggesting that DRAP27 is involved in the entry of diphtheria toxin into the target cell.
通过用Vero细胞膜免疫小鼠,分离出一种可阻断白喉毒素与Vero细胞结合的单克隆抗体。该抗体可抑制白喉毒素以及白喉毒素的突变形式CRM197与Vero细胞的结合,从而抑制白喉毒素的细胞毒性。此抗体不直接与白喉毒素的受体分子(DTR14.5)发生反应。免疫沉淀和免疫印迹研究表明,该抗体与一种27 kDa的新型膜蛋白(DRAP27)结合。当白喉毒素受体通过用此抗体制备的亲和柱时,仅在存在DRAP27的情况下受体才会被捕获。这些结果表明,DRAP27和DTR14.5在Vero细胞膜中紧密结合,并且白喉毒素与受体结合的抑制是由于抗体与DRAP27分子的结合。使用125I标记抗体的结合研究表明,细胞表面的DRAP27分子比白喉毒素结合位点多得多。然而,细胞系对白喉毒素的敏感性与细胞表面DRAP27分子的数量之间存在相关性,这表明DRAP27参与了白喉毒素进入靶细胞的过程。