Wang J, Arbuzova A, Hangyás-Mihályné G, McLaughlin S
Department of Physiology and Biophysics, State University of New York, Stony Brook, NY 11794-8661, USA.
J Biol Chem. 2001 Feb 16;276(7):5012-9. doi: 10.1074/jbc.M008355200. Epub 2000 Oct 25.
Both the myristoylated alanine-rich protein kinase C substrate protein (MARCKS) and a peptide corresponding to its basic effector domain, MARCKS-(151-175), inhibit phosphoinositide-specific phospholipase C (PLC)-catalyzed hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP(2)) in vesicles (Glaser, M., Wanaski, S., Buser, C. A., Boguslavsky, V., Rashidzada, W., Morris, A., Rebecchi, M., Scarlata, S. F., Runnels, L. W., Prestwich, G. D., Chen, J., Aderem, A., Ahn, J., and McLaughlin, S. (1996) J. Biol. Chem. 271, 26187-26193). We report here that adding 10-100 nm MARCKS-(151-175) to a subphase containing either PLC-delta or -beta inhibits hydrolysis of PIP(2) in a monolayer and that this inhibition is due to the strong binding of the peptide to PIP(2). Two direct binding measurements, based on centrifugation and fluorescence, show that approximately 10 nm PIP(2), in the form of vesicles containing 0.01%, 0.1%, or 1% PIP(2), binds 50% of MARCKS-(151-175). Both electrophoretic mobility measurements and competition experiments suggest that MARCKS-(151-175) forms an electroneutral complex with approximately 4 PIP(2). MARCKS-(151-175) binds equally well to PI(4,5)P(2) and PI(3,4)P(2). Local electrostatic interactions of PIP(2) with MARCKS-(151-175) contribute to the binding energy because increasing the salt concentration from 100 to 500 mm decreases the binding 100-fold. We hypothesize that the effector domain of MARCKS can bind a significant fraction of the PIP(2) in the plasma membrane, and release the bound PIP(2) upon interaction with Ca(2+)/calmodulin or phosphorylation by protein kinase C.
肉豆蔻酰化富含丙氨酸的蛋白激酶C底物蛋白(MARCKS)及其对应于其碱性效应结构域的肽MARCKS-(151 - 175),均可抑制囊泡中磷酸肌醇特异性磷脂酶C(PLC)催化的磷脂酰肌醇4,5 - 二磷酸(PIP₂)的水解(格拉泽,M.,瓦纳斯基,S.,布瑟,C.A.,博古斯拉夫斯基,V.,拉希扎达,W.,莫里斯,A.,雷贝奇,M.,斯卡拉塔,S.F.,伦内尔斯,L.W.,普雷斯特维奇,G.D.,陈,J.,阿德雷姆,A.,安,J.,和麦克劳克林,S.(1996年)《生物化学杂志》271,26187 - 26193)。我们在此报告,向含有PLC-δ或 -β的亚相中添加10 - 100 nM的MARCKS-(151 - 175)可抑制单层中PIP₂的水解,且这种抑制是由于该肽与PIP₂的强结合所致。基于离心和荧光的两种直接结合测量表明,以含有0.01%、0.1%或1% PIP₂的囊泡形式存在的约10 nM PIP₂可结合50%的MARCKS-(151 - 175)。电泳迁移率测量和竞争实验均表明,MARCKS-(151 - 175)与约4个PIP₂形成电中性复合物。MARCKS-(151 - 175)与PI(4,5)P₂和PI(3,4)P₂的结合能力相当。PIP₂与MARCKS-(151 - 175)的局部静电相互作用对结合能有贡献,因为将盐浓度从100 mM增加到500 mM会使结合力降低100倍。我们推测,MARCKS的效应结构域可结合质膜中相当一部分的PIP₂,并在与Ca²⁺/钙调蛋白相互作用或被蛋白激酶C磷酸化后释放结合的PIP₂。