EFFECTS OF DIACYLGLYCEROLS AND CA2+ ON STRUCTURE OF PHOSPHATIDYLCHOLINE PHOSPHATIDYLSERINE BILAYERS

被引:66
作者
GOLDBERG, EM
LESTER, DS
BORCHARDT, DB
ZIDOVETZKI, R
机构
[1] UNIV CALIF RIVERSIDE,DEPT BIOL,RIVERSIDE,CA 92521
[2] UNIV CALIF RIVERSIDE,DEPT CHEM,RIVERSIDE,CA 92521
[3] NATL INST HLTH,NEURAL SYST SECT,ROCKVILLE,MD 20852
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1016/S0006-3495(94)80788-X
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The combined effects of the diacylglycerols (DAGs) with the various acyl chains and Ca-2+ on the structure of phosphatidylcholine/phosphatidylserine (4:1 mole/mole) bilayers were studied using H-2- and P-31 NMR. The following DAG- and Ca2+-induced bilayer perturbations were identified. 1) Increased tendency to form nonbilayer lipid phases was induced by diolein or stearoylarachidonoylglycerol, and was synergistically enhanced by the addition of Ca2+. 2) ''Transverse'' bilayer perturbation was induced by dioctanoylglycerol. The addition of this DAG caused increased ordering of the phospholipid acyl side chains in the region adjacent to the headgroup, with the concomitant decrease of the order toward the bilayer interior. 3) Separation of the phosphatidylcholine and phosphatidylserine bilayer components was induced by combinations of relatively high (1:5 mole/mole to phosphatidylserine) Ca2+ and 25 mol% (to the phospholipids) of diolein, stearoylarachidonoylglycerol, or oleoylacetylglycerol. 4) Lateral phase separation of the bilayers on the regions of different fluidities was induced by dipalmitin. These physicochemical effects were correlated with the effects of these DAGs and Ca2+ on the activity of protein kinase C. The increased tendency to form nonbilayer lipid phases and the transverse bilayer perturbations correlated with the increased protein kinase C activity, whereas the actual presence of the nonbilayer lipid phases, as well as the separation of the phosphatidylcholine and phosphatidylserine components, was associated with the decrease in the protein kinase C activity. The lateral phase separation of the bilayer on gel-like and liquid crystalline regions did not have an effect on the activity of the enzyme. These results demonstrate the importance of the physicochemical properties of the membranes in the process of activation of protein kinase C.
引用
收藏
页码:382 / 393
页数:12
相关论文
共 64 条
[1]   IMPORTANCE OF PHOSPHATIDYLETHANOLAMINE FOR ASSOCIATION OF PROTEIN-KINASE-C AND OTHER CYTOPLASMIC PROTEINS WITH MEMBRANES [J].
BAZZI, MD ;
YOUAKIM, A ;
NELSESTUEN, GL .
BIOCHEMISTRY, 1992, 31 (04) :1125-1134
[2]   EXTENSIVE SEGREGATION OF ACIDIC PHOSPHOLIPIDS IN MEMBRANES INDUCED BY PROTEIN-KINASE-C AND RELATED PROTEINS [J].
BAZZI, MD ;
NELSESTUEN, GL .
BIOCHEMISTRY, 1991, 30 (32) :7961-7969
[3]  
BELL RM, 1991, J BIOL CHEM, V266, P4661
[4]  
BERRIDGE MJ, 1987, ANNU REV BIOCHEM, V56, P159, DOI 10.1146/annurev.bi.56.070187.001111
[5]   EFFECT OF PHOSPHOLIPID UNSATURATION ON PROTEIN-KINASE-C ACTIVATION [J].
BOLEN, EJ ;
SANDO, JJ .
BIOCHEMISTRY, 1992, 31 (25) :5945-5951
[6]  
BONI LT, 1985, J BIOL CHEM, V260, P819
[7]  
BONI LT, 1992, PROTEIN KINASE C CUR, P102
[8]   EVIDENCE THAT A 2ND STEREOCHEMICAL CENTER IN DIACYLGLYCEROLS DEFINES INTERACTION AT THE RECOGNITION SITE ON PROTEIN KINASE-C [J].
BONSER, RW ;
THOMPSON, NT ;
HODSON, HF ;
BEAMS, RM ;
GARLAND, LG .
FEBS LETTERS, 1988, 234 (02) :341-344
[9]   DEUTERON QUADRUPOLE COUPLING CONSTANTS IN 3 SOLID DEUTERATED PARAFFIN HYDROCARBONS-C2D6, C4D10, C6D14 [J].
BURNETT, LJ ;
MULLER, BH .
JOURNAL OF CHEMICAL PHYSICS, 1971, 55 (12) :5829-&
[10]   STRUCTURAL AND CHEMICAL SPECIFICITY OF DIRADYLGLYCEROLS FOR PROTEIN KINASE-C ACTIVATION [J].
CABOT, MC ;
JAKEN, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 125 (01) :163-169