Hashimoto T, Kuwabara T, Usuda N, Nagata T
J Biochem. 1986 Aug;100(2):301-10. doi: 10.1093/oxfordjournals.jbchem.a121716.
Peroxisomes were obtained by sucrose density gradient centrifugation from the livers of di(2-ethylhexyl)phthalate-fed rats, and the membranes were prepared by carbonate extraction (Fujiki, Y., Fowler, S., Shio, H., Hubbard, A.L., & Lazarow, P.B. (1982) J. Cell Biol. 93, 103-110). The integrated membrane polypeptides were solubilized with sodium dodecyl sulfate, and purified by repeated polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate. Separation of 70 and 68 kDa polypeptides was not attempted in the present study because of their close migration in polyacrylamide gel electrophoresis. Other polypeptides with apparent molecular masses of 41, 27, 26, and 22 kDa were purified to near homogeneity. Antibodies were raised against these purified preparations. The 68 kDa polypeptide is suggested to be produced by the proteolytic modification of 70 kDa polypeptide, since the former increased concomitantly with decrease of the latter when the liver homogenate was incubated, and this change was prevented in the presence of leupeptin during the incubation. The 41 kDa polypeptide was a minor component. The 70 and 68 kDa polypeptides and 41 kDa polypeptide and their antibodies were cross-reactive, but the relation of these polypeptides was not clear. The 27 and 26 kDa polypeptides seemed to be another species of membrane polypeptides, although the relationship of these two polypeptides remains to be clarified. The 22 kDa polypeptide is not related to other membrane polypeptides. The results of immunoblot analysis of subcellular fractions of the liver and an electron microscopic immunocytochemical study to locate the antigenic sites with protein A-gold complex suggest that all of these polypeptides are localized on peroxisomal membranes. On proliferation of rat liver peroxisomes by administration of di(2-ethylhexyl)phthalate, a peroxisome proliferator, all of these polypeptides were markedly increased.
通过蔗糖密度梯度离心从喂食邻苯二甲酸二(2-乙基己基)酯的大鼠肝脏中获得过氧化物酶体,并用碳酸盐抽提法制备膜(藤木洋、福勒、盐屋浩、哈伯德、拉扎罗夫,1982年,《细胞生物学杂志》93卷,103 - 110页)。整合膜多肽用十二烷基硫酸钠溶解,并在十二烷基硫酸钠存在下通过反复聚丙烯酰胺凝胶电泳进行纯化。由于70 kDa和68 kDa多肽在聚丙烯酰胺凝胶电泳中的迁移距离相近,本研究未尝试对它们进行分离。其他表观分子量为41、27、26和22 kDa的多肽被纯化至接近均一。针对这些纯化制剂制备了抗体。68 kDa多肽被认为是由70 kDa多肽的蛋白水解修饰产生的,因为当肝脏匀浆孵育时,前者随后者的减少而同时增加,并且在孵育过程中亮抑酶肽存在时这种变化被阻止。41 kDa多肽是次要成分。70 kDa和68 kDa多肽以及41 kDa多肽与其抗体具有交叉反应性,但这些多肽之间的关系尚不清楚。27 kDa和26 kDa多肽似乎是另一类膜多肽,尽管这两种多肽之间的关系仍有待阐明。22 kDa多肽与其他膜多肽无关。肝脏亚细胞组分的免疫印迹分析结果以及用蛋白A - 金复合物定位抗原位点的电子显微镜免疫细胞化学研究表明,所有这些多肽都定位于过氧化物酶体膜上。通过给予过氧化物酶体增殖剂邻苯二甲酸二(2-乙基己基)酯使大鼠肝脏过氧化物酶体增殖时,所有这些多肽都显著增加。