Molday R S, Hicks D, Molday L
Invest Ophthalmol Vis Sci. 1987 Jan;28(1):50-61.
Monoclonal antibodies were used with radioimmune assays and immunocytochemical techniques to identify and localize membrane proteins in bovine rod outer segment (ROS) disc membranes. When ROS membrane proteins were separated by SDS-polyacrylamide gel electrophoresis in the presence of the sulfhydryl reducing agent, 2-mercaptoethanol, two monoclonal antibodies designated as 3B6 and 2B6 were found to bind to a polypeptide having an apparent molecular weight (Mr) of 33,000 daltons. In the absence of 2-mercaptoethanol, these monoclonal antibodies bound to a doublet having Mr of 67,000 and 69,000. Immunogold-dextran labeling of ROS sections embedded in Lowicryl resin indicated that this protein is localized around the periphery of the ROS organelle where the discs come in close contact to the ROS plasma membrane. Immunogold labeling of morphologically intact isolated discs prepared by mild trypsinization of ROS fragments confirmed that this disc membrane protein is localized along the rim region of discs. On the basis of these localization studies, the authors have named this protein peripherin. Immunogold-dextran markers were also used with previously characterized antirhodopsin monoclonal antibodies to visualize the distribution of rhodopsin on isolated discs. Dense labeling was observed along the lamellar region of the discs, but little if any labeling was observed on the extreme edges of the discs. These results are consistent with the view that the lamellar region of discs containing rhodopsin is a distinct membrane domain from the rim region which contains peripherin, a high Mr rim protein and possibly other proteins involved in disc-disc and disc-plasma membrane interactions.
单克隆抗体被用于放射免疫分析和免疫细胞化学技术,以鉴定和定位牛视杆细胞外段(ROS)盘膜中的膜蛋白。当在巯基还原剂2-巯基乙醇存在的情况下,通过SDS-聚丙烯酰胺凝胶电泳分离ROS膜蛋白时,发现两种名为3B6和2B6的单克隆抗体与一种表观分子量(Mr)为33,000道尔顿的多肽结合。在没有2-巯基乙醇的情况下,这些单克隆抗体与Mr为67,000和69,000的双峰结合。对包埋在Lowicryl树脂中的ROS切片进行免疫金-葡聚糖标记表明,这种蛋白质位于ROS细胞器的周边,即盘与ROS质膜紧密接触的地方。对通过轻度胰蛋白酶消化ROS片段制备的形态完整的分离盘进行免疫金标记证实,这种盘膜蛋白位于盘的边缘区域。基于这些定位研究,作者将这种蛋白质命名为外周蛋白。免疫金-葡聚糖标记物还与先前表征的抗视紫红质单克隆抗体一起使用,以可视化视紫红质在分离盘上的分布。在盘的层状区域观察到密集标记,但在盘的极端边缘几乎没有观察到标记。这些结果与以下观点一致,即含有视紫红质的盘的层状区域是一个与边缘区域不同的膜结构域,边缘区域含有外周蛋白、一种高分子量边缘蛋白以及可能参与盘-盘和盘-质膜相互作用的其他蛋白质。