Mohamed A H, Steck T L
J Biol Chem. 1986 Feb 25;261(6):2804-9.
Band 3, the anion transport protein of the human erythrocyte membrane, is known to be phosphorylated in ghosts at tyrosine 8. The band 3 tyrosine kinase is now shown to be associated with the Triton X-100 insoluble membrane skeleton but not with spectrin or actin. The kinase was reversibly dissociated from membranes and skeletons at elevated ionic strength (50% at mu = 0.15). The binding capacity of the membranes exceeded their native complement of the kinase by at least 60-fold. Prior removal of all peripheral proteins from the cytoplasmic surface of inside-out vesicles did not diminish the rebinding of the kinase, whereas prior removal of band 3 and other accessory proteins from skeletons abolished the rebinding of the kinase. An excess of glyceraldehyde-3-P dehydrogenase, which binds to band 3 in the region of the phosphate acceptor tyrosine 8, both inhibited the phosphorylation of band 3 and released the kinase into solution. Soluble 40/45-kDa chymotryptic fragments from the cytoplasmic pole of band 3 were phosphorylated at least as well as membranous band 3 and caused the release of the kinase from Triton-extracted skeletons. Membrane skeletons lacked most of the membrane band 3, but retained most of the kinase. Nevertheless, the band 3 population solubilized by Triton X-100 from prelabeled ghosts was as well phosphorylated as the population of band 3 retained by the skeletons. Furthermore, the fraction of band 3 not associated with the skeletons following Triton X-100 extraction was a good substrate for the solubilized kinase. We conclude that this tyrosine kinase is reversibly bound to the membrane through electrostatic interactions with the polyacidic sequence surrounding the phosphate accepting tyrosine 8 on band 3. The kinase appears to be preferentially linked to those band 3 molecules associated with the membrane skeleton, but it impartially phosphorylates band 3 species free in the bilayer as well as band 3 fragments in solution. The resemblance of its plasma membrane binding behavior to that of tyrosine kinases of certain viruses causing oncogenic transformation is discussed.
带3是人红细胞膜的阴离子转运蛋白,已知在血影中其酪氨酸8位点会发生磷酸化。现已表明,带3酪氨酸激酶与Triton X - 100不溶性膜骨架相关联,但与血影蛋白或肌动蛋白无关。在高离子强度(μ = 0.15时为50%)下,该激酶可从膜和骨架上可逆解离。膜的结合能力超过其天然激酶含量至少60倍。事先从外翻小泡的细胞质表面去除所有外周蛋白,并不减少激酶的重新结合,而事先从骨架上去除带3和其他辅助蛋白则消除了激酶的重新结合。过量的甘油醛 - 3 - 磷酸脱氢酶,它在磷酸受体酪氨酸8所在区域与带3结合,既能抑制带3的磷酸化,又能使激酶释放到溶液中。来自带3细胞质端的可溶性40/45 kDa胰凝乳蛋白酶片段至少与膜性带3一样容易被磷酸化,并导致激酶从Triton提取的骨架上释放。膜骨架缺乏大部分膜性带3,但保留了大部分激酶。然而,Triton X - 100从预先标记的血影中溶解的带3群体与骨架保留的带3群体一样容易被磷酸化。此外,Triton X - 100提取后未与骨架相关联的带3部分是溶解的激酶的良好底物。我们得出结论,这种酪氨酸激酶通过与带3上磷酸接受酪氨酸8周围的多酸性序列的静电相互作用,可逆地结合到膜上。该激酶似乎优先与那些与膜骨架相关的带3分子相连,但它能公平地磷酸化双层中游离的带3种类以及溶液中的带3片段。讨论了其质膜结合行为与某些导致致癌转化的病毒的酪氨酸激酶的相似性。