Smith T M, Carl S A, Kirley T L
Department of Pharmacology and Cell Biophysics, University of Cincinnati College of Medicine, Ohio 45267-0575, USA.
Biochem Mol Biol Int. 1998 Aug;45(5):1057-66. doi: 10.1002/iub.7510450523.
We have generated a polyclonal antibody (CKG2) against native chicken gizzard ecto-ATPase for immunolocalization and immunoprecipitation. Active ecto-ATPase is immunoprecipitated from solubilized chicken and rat membranes and shown to be localized to the plasma membrane of the chicken smooth muscle cells. This antibody is specific for the ecto-ATPases, since the more abundant chicken stomach ecto-apyrase is not recognized in immunoprecipitation, western blot or immunolocalization analyses. The CKG2 antibody cross-reacts with mammalian (rat) ecto-ATPase in western blots, with testis being the most abundant source. Interestingly, when the same rat membranes are analyzed by western blot under non-reducing conditions, the 66 kDa ecto-ATPase is not recognized, instead a 200 kDa protein is detected, previously postulated to be an oligomer of ecto-ATPase. However, this 200 kDa cross-reacting protein is not related to the ecto-ATPases, but is instead an immunoglobulin binding protein, comprised of 50 kDa subunits.
我们制备了一种针对天然鸡砂囊胞外ATP酶的多克隆抗体(CKG2),用于免疫定位和免疫沉淀。活性胞外ATP酶可从溶解的鸡和大鼠膜中免疫沉淀出来,并显示定位于鸡平滑肌细胞的质膜。该抗体对胞外ATP酶具有特异性,因为在免疫沉淀、蛋白质免疫印迹或免疫定位分析中,含量更丰富的鸡胃胞外腺苷三磷酸双磷酸酶未被识别。在蛋白质免疫印迹中,CKG2抗体与哺乳动物(大鼠)胞外ATP酶发生交叉反应,其中睾丸是最丰富的来源。有趣的是,当在非还原条件下通过蛋白质免疫印迹分析相同的大鼠膜时,66 kDa的胞外ATP酶未被识别,而是检测到一种200 kDa的蛋白质,之前推测它是胞外ATP酶的寡聚体。然而,这种200 kDa的交叉反应蛋白与胞外ATP酶无关,而是一种由50 kDa亚基组成的免疫球蛋白结合蛋白。