Ling E, Danilov Y N, Cohen C M
Department of Biomedical Research, St. Elizabeth's Hospital, Boston, Massachusetts 02135.
J Biol Chem. 1988 Feb 15;263(5):2209-16.
Human erythrocyte protein 4.1 is phosphorylated in vivo by several protein kinases including protein kinase C and cAMP-dependent kinase. We have used cAMP-dependent kinase purified from red cells and protein kinase C purified from brain to test the effects of phosphorylation on band 4.1 function. In solution, each kinase catalyzed the incorporation of 1-4 mol of PO4/mol of band 4.1. Phosphorylation of band 4.1 by each kinase resulted in a significant (50-80%) reduction in the ability of band 4.1 to promote spectrin binding to F-actin. Direct measurement of spectrin-band 4.1 binding showed that phosphorylation by each kinase also caused dramatic reduction in this association. Phosphorylation of band 4.1 by each kinase for increasing time periods enabled us to demonstrate an approximately linear inverse relationship between PO4 incorporation into band 4.1 and spectrin binding. These results show that phosphorylation of band 4.1 by cAMP-dependent kinase and protein kinase C may be central to the regulation of red cell cytoskeletal organization and membrane mechanical properties.
人类红细胞蛋白4.1在体内可被多种蛋白激酶磷酸化,包括蛋白激酶C和cAMP依赖性激酶。我们使用从红细胞中纯化的cAMP依赖性激酶和从脑中纯化的蛋白激酶C来测试磷酸化对4.1带功能的影响。在溶液中,每种激酶催化每摩尔4.1带掺入1 - 4摩尔的磷酸根。每种激酶对4.1带的磷酸化导致4.1带促进血影蛋白与F - 肌动蛋白结合的能力显著降低(50 - 80%)。血影蛋白与4.1带结合的直接测量表明,每种激酶的磷酸化也导致这种结合显著减少。每种激酶对4.1带进行不同时间段的磷酸化,使我们能够证明4.1带中磷酸根掺入量与血影蛋白结合之间存在近似线性的反比关系。这些结果表明,cAMP依赖性激酶和蛋白激酶C对4.1带的磷酸化可能是调节红细胞细胞骨架组织和膜机械性能的核心。