Tan A W, Nuttall F Q
Biochim Biophys Acta. 1978 Jan 12;522(1):139-50. doi: 10.1016/0005-2744(78)90330-3.
Synthase phosphatase, phosphorylase phosphatase and histone phosphatase in rat liver were measured using as substrates purified liver synthase D, phosphorylase alpha and 32P-labelled phosphorylated f1 histone, respectively. The three phosphatase enzymes had different sedimentation characteristics. Both synthase phosphatase and phosphorylase phosphatase were found to sediment with the microsomal fraction under our experimental conditions. Only 10% of histone phosphatase was in this fraction; the majority was in the cytosol. No change in histone phosphatase was observed in the adrenalectomized fasted rat whereas synthase phosphatase and phosphorylase phosphatase activities were decreased 5-10 fold. Fractionation of liver extract with ethanol produced a dissociation of the three phosphatase activities. When a partially purified fraction was put on a DEAE-cellulose column, synthase phosphatase and phosphorylase phosphatase both exhibited broad elution profiles but their activity peaks did not coincide. Histone phosphatase eluted as a single discrete peak. When the supernatant of CaCl2-treated microsomal fraction was put on a Sepharose 4B column, the majority of synthase phosphatase was found to elute with the larger molecular weight proteins whereas the majority of phosphorylase phosphatase eluted with the smaller species. Histone phosphatase migrated as a single peak and was of intermediate size. Synthase phosphorylase phosphatase by synthase D (Ki approximately 2 units/ml). The inhibition of synthase phosphatase by phosphorylase alpha was kinetically non-competitive with substrate. Histone phosphatase activity was not inhibited by synthase D or by phosphorylase alpha. The above results suggest that different proteins are involved in the dephosphorylation of synthase D, phosphorylase alpha and histone in the cell.
分别使用纯化的肝脏合酶D、磷酸化酶α和32P标记的磷酸化f1组蛋白作为底物,测定大鼠肝脏中的合酶磷酸酶、磷酸化酶磷酸酶和组蛋白磷酸酶。这三种磷酸酶具有不同的沉降特性。在我们的实验条件下,发现合酶磷酸酶和磷酸化酶磷酸酶都与微粒体部分一起沉降。只有10%的组蛋白磷酸酶在该部分;大部分在细胞质中。在肾上腺切除的禁食大鼠中未观察到组蛋白磷酸酶的变化,而合酶磷酸酶和磷酸化酶磷酸酶的活性降低了5至10倍。用乙醇对肝脏提取物进行分级分离导致三种磷酸酶活性解离。当将部分纯化的级分加载到DEAE-纤维素柱上时,合酶磷酸酶和磷酸化酶磷酸酶都表现出较宽的洗脱图谱,但它们的活性峰不一致。组蛋白磷酸酶作为单个离散峰洗脱。当将氯化钙处理的微粒体部分的上清液加载到琼脂糖4B柱上时,发现大部分合酶磷酸酶与较大分子量的蛋白质一起洗脱,而大部分磷酸化酶磷酸酶与较小的蛋白质一起洗脱。组蛋白磷酸酶迁移为单个峰,大小居中。合酶D对合酶磷酸化酶磷酸酶的抑制作用(Ki约为2单位/毫升)。磷酸化酶α对合酶磷酸酶的抑制在动力学上与底物非竞争性。组蛋白磷酸酶活性不受合酶D或磷酸化酶α的抑制。上述结果表明,细胞中合酶D、磷酸化酶α和组蛋白的去磷酸化涉及不同的蛋白质。