Hasegawa M, Watanabe A, Takio K, Suzuki M, Arai T, Titani K, Ihara Y
Department of Neuropathology, Faculty of Medicine, University of Tokyo, Japan.
J Neurochem. 1993 Jun;60(6):2068-77. doi: 10.1111/j.1471-4159.1993.tb03491.x.
Two monoclonal antibodies C5 and M4 raised against Sarkosyl-insoluble paired helical filaments (PHF) specifically labeled fetal tau, but hardly labeled normal adult tau. C5 immunoreactivity was eliminated by alkaline phosphatase treatment at 37 degrees C, whereas M4 reactivity could be removed only by the treatment at 67 degrees C. Epitope analysis showed that C5 and M4 recognition sites are in residues 386-406 and 198-250, respectively, according to the numbering of the longest human tau isoform. Thus, the phosphorylation sites are located in the amino- and carboxyl-terminal portions of the microtubule-binding region. These two well-characterized monoclonals should be valuable in the identification of a protein kinase(s) that converts normal tau into PHF-tau.
两种针对十二烷基肌氨酸钠不溶性双螺旋丝(PHF)产生的单克隆抗体C5和M4特异性标记胎儿tau蛋白,但几乎不标记正常成人tau蛋白。C5免疫反应性在37℃经碱性磷酸酶处理后消除,而M4反应性仅在67℃处理时才能去除。表位分析表明,根据最长的人类tau异构体的编号,C5和M4识别位点分别在残基386 - 406和198 - 250中。因此,磷酸化位点位于微管结合区域的氨基和羧基末端部分。这两种特性明确的单克隆抗体在鉴定将正常tau蛋白转化为PHF - tau蛋白的蛋白激酶方面应具有重要价值。