Haasemann M, Figueroa C D, Henderson L, Grigoriev S, Abd Alla S, Gonzalez C B, Dunia I, Hoebeke J, Jarnagin K, Cartaud J
Institut Jacques Monod, CNRS, Université Paris VII, France.
Braz J Med Biol Res. 1994 Aug;27(8):1739-56.
Peptides corresponding to sequences derived from predicted extra- and intracellular loops of the rat bradykinin receptor were analyzed for interspecies homology as well as for matches within the present dataset of protein sequences to provide a theoretical basis for the specific recognition of the native cognate protein by antibodies raised against these antigens. Application of polyclonal antibodies raised against the selected peptides allowed the immunocytochemical localization of the native receptor protein in cells of rat and human origin. The detection of the molecule was achieved by different immunohisto- and immunocytochemical methods in combination with light, fluorescence, confocal optical laser and electron microscopy. These results were compared to localization studies by autoradiography. Distribution and subcellular localization were determined in human neutrophils, human epithelial carcinoma cells (A431) and in rat kidney tissue.
分析了与源自大鼠缓激肽受体预测的细胞外和细胞内环序列相对应的肽,以研究种间同源性以及在当前蛋白质序列数据集中的匹配情况,从而为针对这些抗原产生的抗体特异性识别天然同源蛋白提供理论依据。应用针对所选肽产生的多克隆抗体,可对大鼠和人源细胞中的天然受体蛋白进行免疫细胞化学定位。通过不同的免疫组织化学和免疫细胞化学方法结合光镜、荧光、共聚焦光学激光和电子显微镜实现了该分子的检测。将这些结果与放射自显影定位研究进行了比较。在人中性粒细胞、人上皮癌细胞(A431)和大鼠肾脏组织中确定了分布和亚细胞定位。