Huelsenbeck Stefanie C, Klose Ilona, Reichenbach Maria, Huelsenbeck Johannes, Genth Harald
Institut für Toxikologie, Medizinische Hochschule Hannover, D-30625 Hannover, Germany.
FEBS Lett. 2009 Oct 6;583(19):3133-9. doi: 10.1016/j.febslet.2009.09.006. Epub 2009 Sep 8.
Mono-glucosylation of (H/K/N)Ras by Clostridium sordellii lethal toxin (TcsL) blocks critical survival signaling pathways, resulting in apoptotic cell death. One yet unsolved problem in studies on TcsL is the lack of a method allowing the specific detection of (H/K/N)Ras glucosylation. In this study, we identify the Ras(Mab 27H5) antibody as a glucosylation-sensitive antibody capable for the immunoblot detection of (H/K/N)Ras glucosylation in TcsL-treated cells. Alternative Ras antibodies including the K-Ras(Mab F234) antibody or the v-H-Ras(Mab Y13-159) antibody recognize Ras proteins regardless of glucosylation. (H/K)Ras are further shown to be more efficaciously glucosylated by TcsL than Rac1 in rat basophilic leukemia cells as well as in a cell-free system.
索氏梭菌致死毒素(TcsL)对(H/K/N)Ras进行的单糖基化作用会阻断关键的生存信号通路,从而导致细胞凋亡死亡。TcsL研究中一个尚未解决的问题是缺乏一种能够特异性检测(H/K/N)Ras糖基化的方法。在本研究中,我们确定Ras(单克隆抗体27H5)抗体是一种对糖基化敏感的抗体,能够通过免疫印迹法检测TcsL处理细胞中(H/K/N)Ras的糖基化。包括K-Ras(单克隆抗体F234)抗体或v-H-Ras(单克隆抗体Y13-159)抗体在内的其他Ras抗体,无论糖基化与否,均可识别Ras蛋白。在大鼠嗜碱性白血病细胞以及无细胞体系中,(H/K)Ras被证明比Rac1更易被TcsL糖基化。