Koob R, Zimmermann M, Schoner W, Drenckhahn D
Department of Anatomy and Cell Biology, University of Marburg/Federal Republic of Germany.
Eur J Cell Biol. 1988 Feb;45(2):230-7.
Interactions between integral proteins of the plasma membrane and the cytoskeleton may be important for localizing certain membrane proteins in a nonrandom fashion at specialized domains of the cell surface. Here, we show that ankyrin, the key protein for the linkage of the erythrocyte anion exchanger (band 3) to the spectrin-based membrane cytoskeleton, is also present in kidney distal tubular cells where ankyrin is precisely colocalized with Na+,K+-ATPase. Both proteins are confined to the basolateral plasma membrane and are absent from the apical membrane, the junctional complex and the membrane surface that contacts the basal lamina. Purified Na+,K+-ATPase of sheep and pig kidney contains a binding site for erythrocyte ankyrin as demonstrated by immunoprecipitation experiments. A band 3-like binding site for ankyrin is likely, since binding of ankyrin to Na+,K+-ATPase could be inhibited in a competitive fashion by the isolated cytoplasmic domain of erythrocyte band 3.
质膜整合蛋白与细胞骨架之间的相互作用对于将某些膜蛋白以非随机方式定位在细胞表面的特定区域可能很重要。在这里,我们表明锚蛋白是红细胞阴离子交换蛋白(带3)与基于血影蛋白的膜细胞骨架连接的关键蛋白,它也存在于肾远端小管细胞中,在那里锚蛋白与Na +,K + -ATP酶精确共定位。这两种蛋白质都局限于基底外侧质膜,而不存在于顶端膜、连接复合体和与基膜接触的膜表面。免疫沉淀实验表明,绵羊和猪肾纯化的Na +,K + -ATP酶含有红细胞锚蛋白的结合位点。由于红细胞带3的分离细胞质结构域可以竞争性地抑制锚蛋白与Na +,K + -ATP酶的结合,因此可能存在一个类似于带3的锚蛋白结合位点。