Inhorn R C, Majerus P W
Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.
J Biol Chem. 1988 Oct 5;263(28):14559-65.
We recently described inositol polyphosphate 1-phosphatase, an enzyme which cleaves the 1-phosphate from inositol 1,4-bisphosphate (Ins(1,4)P2) and inositol 1,3,4-trisphosphate (Ins(1,3,4)P3) (Inhorn, R. C., and Majerus, P. W. (1987) J. Biol. Chem. 262, 15946-15952). We have now purified the enzyme to homogeneity from calf brain. The enzyme hydrolyzes 50.3 mumol of Ins(1,4)P2/min/mg protein. The enzyme has an apparent mass of 44,000 daltons as determined both by gel filtration chromatography and by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, suggesting that it is monomeric. Lithium ions inhibit Ins(1,3,4)P3 hydrolysis uncompetitively with an apparent Ki of approximately 0.3 mM LiCl. Calcium inhibits hydrolysis of Ins(1,4)P2 and Ins(1,3,4)P3 equally, with approximately 40% inhibition occurring at 1 microM free Ca2+. Rabbit polyclonal antiserum against purified inositol polyphosphate 1-phosphatase was prepared which immunoprecipitates approximately 0.3 milliunits of activity/microliter serum (1 unit = 1 mumol of Ins(1,4)P2 hydrolyzed per min). This antiserum was used to determine the enzyme content in several bovine tissues, all of which had a similar intrinsic specific activity (i.e. approximately 0.3 milliunits/microliter antiserum). Tissues studied included brain, heart, kidney, liver, lung, parotid, spleen, testis, and thymus. Approximately 10-15% of the total inositol polyphosphate 1-phosphatase activity in calf brain homogenates remains in a particulate fraction; antiserum also binds 0.3 milliunits of membrane-associated activity/microliter antiserum. Thus, a single enzyme can account for Ins(1,4)P2 hydrolytic activity in the bovine tissues. Ins(1,3,4)P3 metabolism was also investigated in bovine tissue homogenates. Inositol polyphosphate 1-phosphatase accounts for greater than 80% of the hydrolytic activity in all tissues studied except brain, where inositol polyphosphate 4-phosphatase is the major enzyme that hydrolyzes Ins(1,3,4)P3. The apparent Km of inositol polyphosphate 1-phosphatase for Ins(1,3,4)P3 varies approximately 3-4-fold among the bovine tissues.
我们最近描述了肌醇多磷酸1 - 磷酸酶,一种能从肌醇1,4 - 二磷酸(Ins(1,4)P2)和肌醇1,3,4 - 三磷酸(Ins(1,3,4)P3)上裂解1 - 磷酸的酶(英霍恩,R.C.,和马耶鲁斯,P.W.(1987年)《生物化学杂志》262卷,15946 - 15952页)。我们现在已从小牛脑中纯化出该酶至均一状态。该酶每分钟每毫克蛋白质可水解50.3微摩尔的Ins(1,4)P2。通过凝胶过滤色谱法和十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳测定,该酶的表观分子量为44,000道尔顿,表明它是单体形式。锂离子以非竞争性方式抑制Ins(1,3,4)P3的水解,其表观Ki约为0.3 mM LiCl。钙离子对Ins(1,4)P2和Ins(1,3,4)P3水解的抑制作用相同,在游离Ca2 +浓度为1 microM时约有40%的抑制率。制备了针对纯化的肌醇多磷酸1 - 磷酸酶的兔多克隆抗血清,其每微升血清可免疫沉淀约0.3毫单位的活性(1单位 = 每分钟水解1微摩尔Ins(1,4)P2)。该抗血清用于测定几种牛组织中的酶含量,所有这些组织的内在比活性相似(即每微升抗血清约0.3毫单位)。研究的组织包括脑、心脏、肾脏、肝脏、肺、腮腺、脾脏、睾丸和胸腺。小牛脑匀浆中总肌醇多磷酸1 - 磷酸酶活性的约10 - 15%保留在颗粒部分;抗血清每微升还能结合0.3毫单位的膜相关活性。因此,单一酶可解释牛组织中Ins(1,4)P2的水解活性。还对牛组织匀浆中的Ins(1,3,4)P3代谢进行了研究。除脑外,在所有研究的组织中,肌醇多磷酸1 - 磷酸酶占水解活性的80%以上,在脑中,肌醇多磷酸4 - 磷酸酶是水解Ins(1,3,4)P3的主要酶。肌醇多磷酸1 - 磷酸酶对Ins(1,3,4)P3的表观Km在牛组织之间变化约3 - 4倍。