Wheeler M B, Veldhuis J D
Mol Cell Endocrinol. 1987 Mar;50(1-2):123-9. doi: 10.1016/0303-7207(87)90084-0.
We have evaluated the catalytic and receptor-binding properties of protein kinase C in swine luteal cytosol using two complementary approaches: assay of catalytic activity assessed as the enzymatic transfer of radiolabeled phosphate to histone III-s acceptor protein in the presence of specific phospholipid, diacylglycerol, or phorbol ester and ionic calcium; and, the high-affinity binding of [3H]phorbol-12,13-dibutyrate ([3H]PDB) to the protein kinase C receptor. Catalytic properties of pig luteal protein kinase C included: absolute dependence on calcium ions for maximal activation (approximate ka = 0.5 microM); synergistic activation by 1,2-sn-diolein, phospholipid and calcium ions; and rank order of specific phospholipid activational potency: phosphatidylserine greater than phosphatidic acid greater than phosphatidylinositol greater than phosphatidylethanolamine greater than phosphatidylcholine. The enzyme was also activated by specific phorbol esters at the following half-maximally effective (ED50) concentrations: 12-O-tetradecanoylphorbol-13-acetate (TPA) 11 nM; phorbol-12,13-dibenzoate (PDBe) 26 nM; phorbol-12,13-dibutyrate (PDBu) 33 nM; mezerein 65 nM; and phorbol-12,13-diacetate (PDA) 130 nM. Phorbol-ester receptor properties of protein kinase C included specific, high-affinity (kd congruent to 19 nM), saturable, low-capacity (congruent to 44 pmol/mg protein) [3H]PDB binding sites. Moreover, the rank order of the equilibrium binding ID50s for various phorbol compounds was similar to that of catalytic ED50s: viz. 3 nM TPA; 8 nM PDBe; 16 nM PDBu; 19 nM mezerein; and 590 nM PDA. Thus, swine luteal cytosol contains catalytically active protein kinase C with specific phospholipid sensitivity, synergistic activation by diacylglycerol, phospholipid and calcium, and a strict dependence on ionic calcium concentrations that is influenced markedly by the presence of diacylglycerol.(ABSTRACT TRUNCATED AT 250 WORDS)
我们采用两种互补方法评估了猪黄体细胞质中蛋白激酶C的催化和受体结合特性:一是在特定磷脂、二酰基甘油、佛波酯和离子钙存在的情况下,通过测定放射性标记的磷酸基团向组蛋白III-s受体蛋白的酶促转移来评估催化活性;二是测定[3H]佛波醇-12,13-二丁酸酯([3H]PDB)与蛋白激酶C受体的高亲和力结合。猪黄体蛋白激酶C的催化特性包括:最大激活对钙离子有绝对依赖性(近似解离常数ka = 0.5微摩尔);1,2-二油酰甘油、磷脂和钙离子协同激活;特定磷脂激活效力的排序为:磷脂酰丝氨酸>磷脂酸>磷脂酰肌醇>磷脂酰乙醇胺>磷脂酰胆碱。该酶也可被特定佛波酯在以下半数最大有效(ED50)浓度下激活:12-O-十四酰佛波醇-13-乙酸酯(TPA)11纳摩尔;佛波醇-12,13-二苯甲酸酯(PDBe)26纳摩尔;佛波醇-12,13-二丁酸酯(PDBu)33纳摩尔;大戟二萜醇65纳摩尔;佛波醇-12,13-二乙酸酯(PDA)130纳摩尔。蛋白激酶C的佛波酯受体特性包括特异性、高亲和力(解离常数kd约为19纳摩尔)、可饱和、低容量(约44皮摩尔/毫克蛋白)的[3H]PDB结合位点。此外,各种佛波化合物平衡结合ID50s的排序与催化ED50s的排序相似,即:TPA 3纳摩尔;PDBe 8纳摩尔;PDBu 16纳摩尔;大戟二萜醇19纳摩尔;PDA 590纳摩尔。因此,猪黄体细胞质中含有具有催化活性的蛋白激酶C,其对特定磷脂敏感,受二酰基甘油、磷脂和钙离子协同激活,且对离子钙浓度有严格依赖性,二酰基甘油的存在会显著影响这一依赖性。(摘要截短至250字)