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FA/GSK-3与酪蛋白激酶II协同磷酸化并激活ATP-镁依赖性磷蛋白磷酸酶(PC0.7) 。

Synergistic phosphorylation and activation of ATP-Mg-dependent phosphoprotein phosphatase by F A/GSK-3 and casein kinase II (PC0.7).

作者信息

DePaoli-Roach A A

出版信息

J Biol Chem. 1984 Oct 10;259(19):12144-52.

PMID:6090457
Abstract

The ATP-Mg-dependent phosphoprotein phosphatase is believed to consist of a catalytic subunit and a regulatory component identified as phosphatase inhibitor-2. It was found in this study that isolated inhibitor-2 was phosphorylated in serine residues by casein kinase II to at least 3 mol of phosphate per mol of inhibitor-2 while another protein kinase, F A/GSK-3, introduced no more than 0.3 mol of phosphate per mol exclusively in threonine residues. Analysis of tryptic digests by high performance liquid chromatography indicated that casein kinase II action resulted in two major (peaks 1 and 2) and two minor phosphopeptides whereas F A/GSK-3 action generated only peak 2. Combined action of the two protein kinases introduced an additional 0.4-0.6 mol of phosphate per mol over that predicted for simple additive behavior. This synergistic phosphorylation was associated with increased phosphate in peak 2 and correlated with unchanged phosphoserine but increased phosphothreonine, to a level approaching 1 mol/mol. ATP-Mg-dependent protein phosphatase was either reconstituted from purified inhibitor-2 and low molecular weight type 1 phosphatase or isolated as an inactive complex (Fc). Both phosphatase complexes were activated by F A/GSK-3 which caused a transient phosphorylation of the inhibitor-2 component. Casein kinase II alone phosphorylated the inhibitor-2 in both phosphatase complexes without affecting the enzyme activity. Exposure to the combination of F A/GSK-3 and casein kinase II resulted in a synergistic phosphorylation. Furthermore, the combined action of the two protein kinases caused a synergistic activation of the phosphatase at submaximal F A/GSK-3 levels. The results suggest that interactions between phosphorylation sites may play a role in the activation of the ATP-Mg-dependent phosphatase, in particular that phosphorylation by casein kinase II at serine can potentiate the phosphorylation of threonine by F A/GSK-3 with subsequent influence on phosphatase activation.

摘要

据信,ATP-镁依赖性磷蛋白磷酸酶由一个催化亚基和一个被鉴定为磷酸酶抑制剂-2的调节成分组成。本研究发现,分离出的抑制剂-2被酪蛋白激酶II磷酸化于丝氨酸残基,每摩尔抑制剂-2至少有3摩尔磷酸盐,而另一种蛋白激酶F A/GSK-3每摩尔仅在苏氨酸残基引入不超过0.3摩尔磷酸盐。通过高效液相色谱分析胰蛋白酶消化产物表明,酪蛋白激酶II的作用产生了两个主要的(峰1和峰2)和两个次要的磷酸肽,而F A/GSK-3的作用仅产生峰2。两种蛋白激酶的联合作用每摩尔引入的磷酸盐比简单加和行为预测的多0.4 - 0.6摩尔。这种协同磷酸化与峰2中磷酸盐增加有关,与磷酸丝氨酸不变但磷酸苏氨酸增加相关,达到接近1摩尔/摩尔的水平。ATP-镁依赖性蛋白磷酸酶要么由纯化的抑制剂-2和低分子量1型磷酸酶重构而成,要么作为无活性复合物(Fc)分离出来。两种磷酸酶复合物都被F A/GSK-3激活,这导致抑制剂-2成分的瞬时磷酸化。单独的酪蛋白激酶II使两种磷酸酶复合物中的抑制剂-2磷酸化,而不影响酶活性。暴露于F A/GSK-3和酪蛋白激酶II的组合导致协同磷酸化。此外,两种蛋白激酶的联合作用在亚最大F A/GSK-3水平下导致磷酸酶的协同激活。结果表明,磷酸化位点之间的相互作用可能在ATP-镁依赖性磷酸酶的激活中起作用,特别是酪蛋白激酶II在丝氨酸处的磷酸化可以增强F A/GSK-3在苏氨酸处的磷酸化,随后影响磷酸酶的激活。

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