Bacha P, Murphy J R, Moynihan M
J Biol Chem. 1980 Nov 25;255(22):10658-62.
The Mr = 62,000 diphtheria toxin-related proteins produced from the suppression of nonsense mutations within the tox gene of corynephage beta were purified by affinity chromatography. Except for the toxin 111-sup2-62, the Mr = 62,000 polypeptides were found to have the same specific toxicity as does wild type toxin. 111-sup2-62 was found to have a prolonged lag period prior to the onset of inhibition of protein synthesis and ADP-ribosylation of elongation factor 2. 111-sup2-62 differs from wild type toxin by an amino acid substitution at a site approximatley 47,000 daltons from the NH2 terminus. The data presented provide genetic support for the Boquet-Pappenheimer model (Boquet, P., and Pappenheimer, A. M. Jr (1978) J. Biol. Chem. 251, 5770-5778) of fragment A translocation into the eukaryotic cell cytosol.
通过亲和层析法纯化了由β棒状噬菌体tox基因内无义突变抑制产生的Mr = 62,000的白喉毒素相关蛋白。除毒素111-sup2-62外,发现Mr = 62,000的多肽与野生型毒素具有相同的比毒性。发现111-sup2-62在抑制蛋白质合成和延伸因子2的ADP-核糖基化开始之前具有延长的延迟期。111-sup2-62与野生型毒素的不同之处在于,在距NH2末端约47,000道尔顿的位点存在氨基酸取代。所提供的数据为Boquet-Pappenheimer模型(Boquet, P.,和Pappenheimer, A. M. Jr (1978) J. Biol. Chem. 251, 5770 - 5778)中片段A易位到真核细胞胞质溶胶提供了遗传学支持。