Kotani S, Murofushi H, Maekawa S, Aizawa H, Kaji K, Sakai H
Cell Struct Funct. 1987 Feb;12(1):1-9. doi: 10.1247/csf.12.1.
We previously investigated the biochemical characteristics of microtubule-associated proteins (MAPs) of the adrenal medulla and adrenal cortex and found that they contain a new kind of MAP with a molecular weight of 190,000 (190 kD MAP) as a major species (Kotani, S., H. Murofushi, S. Maekawa, C. Sato, and H. Sakai. Eur. J. Biochem. 156, 23-29, 1986). We now have used an affinity purified anti-(190 kD MAP) antibody and show by indirect immunofluorescent microscopy the association of this MAP with microtubules in situ in TIG-3 cells (human embryonic lung fibroblasts). The 190 kD MAP was present along the interphase and mitotic microtubules, and there was no marked difference between the staining pattern with anti-tubulin and that with anti-(190 kD MAP) antibodies, evidence that the localization of 190 kD MAP is not restricted to the subset of microtubules. We also isolated MAPs from TIG-3 cells and identified their 190 kD MAP as a major heat-stable component. Several other unidentified polypeptides were recovered in the MAP fraction specifically.
我们之前研究了肾上腺髓质和肾上腺皮质微管相关蛋白(MAPs)的生化特性,发现它们含有一种分子量为190,000的新型MAP(190 kD MAP)作为主要成分(小谷,S.,H. 室伏,S. 前川,C. 佐藤,和H. 酒井。欧洲生物化学杂志156,23 - 29,1986)。我们现在使用亲和纯化的抗(190 kD MAP)抗体,并通过间接免疫荧光显微镜显示这种MAP与TIG - 3细胞(人胚肺成纤维细胞)原位微管的关联。190 kD MAP存在于间期和有丝分裂微管中,抗微管蛋白抗体和抗(190 kD MAP)抗体的染色模式之间没有明显差异,这表明190 kD MAP的定位并不局限于微管的子集。我们还从TIG - 3细胞中分离出MAPs,并将其190 kD MAP鉴定为主要的热稳定成分。在MAP组分中还特异性地回收了其他几种未鉴定的多肽。