Cieplak W, Gaudin H M, Eidels L
Department of Microbiology, University of Texas Health Science Center at Dallas 75235.
J Biol Chem. 1987 Sep 25;262(27):13246-53.
The biochemical characteristics of specific receptor molecules for diphtheria toxin on the surface of two toxin-sensitive cell lines (Vero and BS-C-1) were examined. Diphtheria toxin was found to bind to a number of different proteins in Nonidet P-40 solubilized extracts of 125I-labeled cells. In contrast, permitting diphtheria toxin to bind first to labeled intact cells, which were subsequently solubilized and subjected to immunoprecipitation with anti-diphtheria toxin, resulted in a far more restricted profile of diphtheria toxin-binding proteins that possessed Mrs in the range of 10,000-20,000. Direct chemical cross-linking of radioiodinated diphtheria toxin to cell surface proteins resulted in the appearance of several predominant bands possessing Mrs of approximately 80,000. The Mr approximately 80,000 complexes were shown to be composed of radiolabeled diphtheria toxin (Mr 60,000) and unlabeled Mr approximately 20,000 cellular proteins. These complexes were judged to be a result of specific binding in that their appearance could be preferentially inhibited by the addition of a 100-fold excess of unlabeled diphtheria toxin. The formation of the Mr approximately 80,000 complexes was sensitive to prior trypsin treatment of the cells and to known inhibitors of diphtheria toxin binding. Furthermore, prior incubation of the cells with diphtheria toxin at 37 degrees C ("down regulation") markedly and specifically reduced the subsequent formation of the Mr approximately 80,000 cross-linked complexes, and these down-regulated cells were less sensitive to diphtheria toxin in cytotoxicity assays. Further incubation of down-regulated cells at 37 degrees C restored their ability to form Mr approximately 80,000 complexes; this regeneration requires protein synthesis and restores the cells' sensitivity to diphtheria toxin-mediated cytotoxicity. These results strongly suggest that a Mr 10,000-20,000 cell surface protein is, or constitutes a portion of, the functional diphtheria toxin receptor.
研究了两种毒素敏感细胞系(Vero和BS - C - 1)表面白喉毒素特异性受体分子的生化特性。发现白喉毒素能与125I标记细胞的Nonidet P - 40溶解提取物中的多种不同蛋白质结合。相比之下,先让白喉毒素与标记的完整细胞结合,随后将细胞溶解并用抗白喉毒素进行免疫沉淀,得到的白喉毒素结合蛋白谱则受到更多限制,这些蛋白的相对分子质量在10,000 - 20,000范围内。将放射性碘化白喉毒素直接化学交联到细胞表面蛋白上,出现了几条相对分子质量约为80,000的主要条带。相对分子质量约为80,000的复合物显示由放射性标记的白喉毒素(相对分子质量60,000)和未标记的相对分子质量约为20,000的细胞蛋白组成。这些复合物被认为是特异性结合的结果,因为加入100倍过量的未标记白喉毒素可优先抑制它们的出现。相对分子质量约为80,000复合物的形成对细胞预先用胰蛋白酶处理以及对白喉毒素结合的已知抑制剂敏感。此外,细胞在37℃下预先用白喉毒素孵育(“下调”)可显著且特异性地减少随后相对分子质量约为80,000交联复合物的形成,并且这些下调的细胞在细胞毒性测定中对白喉毒素的敏感性降低。下调的细胞在37℃下进一步孵育可恢复其形成相对分子质量约为80,000复合物的能力;这种再生需要蛋白质合成,并恢复细胞对白喉毒素介导的细胞毒性的敏感性。这些结果强烈表明,相对分子质量为10,000 - 20,000的细胞表面蛋白是功能性白喉毒素受体,或构成其一部分。