Olmsted J B, Lyon H D
J Biol Chem. 1981 Apr 10;256(7):3507-11.
A modified procedure is reported that enables microtubule assembly to occur in extracts of differentiated neuroblastoma cells. Of the proteins that co-assemble through five successive cycles, only two, with molecular weights of 215,000 and 71,000, are retained in constant ratio to tubulin. The 215,000-dalton protein is quantitatively sedimented with microtubules during later cycles of assembly, whereas the 71,000-dalton protein is distributed between assembling and nonassembling fractions. Similar procedures do not induce assembly for microtubules from nondifferentiated neuroblastoma cells. Two-dimensional gel analyses indicate that the differentiated cell extracts contain the 215,000-dalton protein. In contrast, gels of extracts from nondifferentiated cells show no protein in the equivalent region. These data suggest that the 215,000-dalton protein is a microtubule-associated protein that may play a role in microtubule-dependent neurite differentiation.
报道了一种改进的方法,该方法能使微管组装在分化的神经母细胞瘤细胞提取物中发生。在通过五个连续循环共同组装的蛋白质中,只有两种蛋白质,分子量分别为215,000和71,000,与微管蛋白保持恒定比例。在组装的后期循环中,215,000道尔顿的蛋白质与微管一起定量沉淀,而71,000道尔顿的蛋白质则分布在组装和未组装部分之间。类似的方法不会诱导未分化神经母细胞瘤细胞的微管组装。二维凝胶分析表明,分化细胞提取物中含有215,000道尔顿的蛋白质。相比之下,未分化细胞提取物的凝胶在等效区域未显示出蛋白质。这些数据表明,215,000道尔顿的蛋白质是一种微管相关蛋白,可能在微管依赖性神经突分化中起作用。