Cifuentes M E, Honkanen L, Rebecchi M J
Department of Physiology and Biophysics, State University of New York, Stony Brook 11794.
J Biol Chem. 1993 Jun 5;268(16):11586-93.
Active proteolytic fragments of phosphoinositide-specific phospholipase C-delta 1 (PLC-delta 1) were generated by trypsin digestion of the native protein. Brief proteolysis produced a 77-kDa fragment that contained the highly conserved X and Y regions but lacked the amino-terminal domain (amino acids 1-60). Prolonged digestion of PLC-delta 1 produced two fragments, one of 45 kDa that contained the entire X region and another of 32 kDa that consisted of the entire Y region and COOH-terminal domain. The 45- and 32-kDa fragments were isolated as an active heterodimeric complex. The 77-kDa fragment and the complex catalyzed calcium-dependent hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) in detergent/phospholipid mixed micelles. When compared with the native enzyme, both the 77-kDa fragment and the complex exhibited a reduced capacity to processively hydrolyze PIP2; increasing the mole fraction of PIP2 in the mixed micelle surface greatly increased the rate of PIP2 hydrolysis catalyzed by the native enzyme but not the fragments. Both fragments also exhibited a reduced affinity for substrate; the native enzyme bound to bilayer vesicles consisting of phosphatidylcholine and PIP2 with high affinity (Ka approximately 10(6) M-1), whereas the fragments bound weakly (Ka < 10(4) M-1). These results demonstrate that the X, Y, and COOH-terminal regions form a calcium-dependent catalytic core that is resistant to proteolysis. The amino-terminal domain appears to be essential for high affinity binding to PIP2 but not catalysis. These observations are consistent with the idea that the amino-terminal domain forms part of a PIP2 binding site, which anchors PLC-delta 1 to the membrane surface during processive hydrolysis of its substrate.
通过用胰蛋白酶消化天然蛋白产生了磷酸肌醇特异性磷脂酶C-δ1(PLC-δ1)的活性蛋白水解片段。短暂的蛋白水解产生了一个77 kDa的片段,该片段包含高度保守的X和Y区域,但缺少氨基末端结构域(氨基酸1 - 60)。对PLC-δ1进行长时间消化产生了两个片段,一个45 kDa的片段包含整个X区域,另一个32 kDa的片段由整个Y区域和羧基末端结构域组成。45 kDa和32 kDa的片段被分离为一种活性异二聚体复合物。77 kDa的片段和该复合物催化了去污剂/磷脂混合胶束中磷脂酰肌醇4,5-二磷酸(PIP2)的钙依赖性水解。与天然酶相比,77 kDa的片段和该复合物连续水解PIP2的能力均降低;增加混合胶束表面PIP2的摩尔分数极大地提高了天然酶催化的PIP2水解速率,但对片段则没有影响。两个片段对底物的亲和力也都降低;天然酶以高亲和力(Ka约为10⁶ M⁻¹)结合由磷脂酰胆碱和PIP2组成的双层囊泡,而片段的结合较弱(Ka < 10⁴ M⁻¹)。这些结果表明,X、Y和羧基末端区域形成了一个对蛋白水解具有抗性的钙依赖性催化核心。氨基末端结构域似乎对于与PIP2的高亲和力结合至关重要,但对催化作用并非必需。这些观察结果与氨基末端结构域构成PIP2结合位点的一部分这一观点一致,该位点在其底物的连续水解过程中将PLC-δ1锚定在膜表面。