Zwiller J, Ogasawara E M, Nakamoto S S, Boynton A L
Cancer Research Center of Hawaii, University of Hawaii, Honolulu 96813.
Biochem Biophys Res Commun. 1988 Sep 15;155(2):767-72. doi: 10.1016/s0006-291x(88)80561-8.
Several inositol trisphosphate isomers and inositol tetrakisphosphate activate a rat brain phosphoprotein phosphatase, using phosphohistone as well as phosphorylase kinase as substrate. Inositol mono- and bisphosphate have no effect. The protein phosphatase may correspond to type-1 since it is associated with the particulate fraction and is inhibited by heparin. Evidence is presented for the target of inositol phosphate being the catalytic subunit of the protein phosphatase. A parallelism is observed between the ability of the several inositol trisphosphates to activate the protein phosphatase and reported data indicating their ability to release calcium in permeabilized cells.
几种肌醇三磷酸异构体和肌醇四磷酸以磷酸组蛋白和磷酸化酶激酶为底物,激活大鼠脑磷蛋白磷酸酶。肌醇一磷酸和二磷酸无此作用。该蛋白磷酸酶可能属于1型,因为它与微粒体部分相关且受肝素抑制。有证据表明肌醇磷酸的作用靶点是该蛋白磷酸酶的催化亚基。观察到几种肌醇三磷酸激活该蛋白磷酸酶的能力与报道的它们在透化细胞中释放钙的能力之间存在平行关系。