|
|
||||||||
Original Article |
Phospholipase A2 activity against mixed monolayers of dilauroylphosphatidic acid or dilauroylphosphatidylcholine with glycosphingolipids can be reversibly modulated by external constant electrostatic fields. The changes of enzymatic activity are correlated to the depolarization or hyperpolarization of the film caused by specific dipolar properties of glycosphingolipids. Hyperpolarizing fields enhance the enzymatic activity against pure dilauroylphosphatidic acid while depolarizing fields induce a decrease of activity. Compared to the pure substrate, the interface of mixed films containing neutral glycosphingolipids or gangliosides is already partially depolarized and the magnitude of activation induced by an external hyperpolarizing field is decreased; conversely, depolarizing fields cause an increased inhibition of activity. Differing from gangliosides, sulfatides bring about a hyperpolarization of the mixed lipid monolayer and external hyperpolarizing or depolarizing fields cause enhanced activation and reduced inhibition, respectively. The effects of glycosphingolipids depend on their relative proportion in the monolayer. Results were similar with dilauroylphosphosphatidylcholine but the field effects were less than half of those found with dilauroylphosphatidic acid.
Our work shows that the activity of phospholipase A2 in addition to responding reversibly to external electrostatic fields, is directly modulated by the polarity and magnitude of the lipid polar head group dipole moments.Maggio, B. Modulation of phospholipase A2 by electrostatic fields and dipole potential of glycosphingolipids in monolayers. J. Lipid Res. 1999. 40: 930939.
Supplementary key words: gangliosides, sulfatides, cerebrosides, enzyme activity in monolayers, surface potential
This article has been cited by other articles:
![]() |
L. Wang, P. S. Bose, and F. J. Sigworth Using cryo-EM to measure the dipole potential of a lipid membrane PNAS, December 5, 2006; 103(49): 18528 - 18533. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Starke-Peterkovic, N. Turner, M. F. Vitha, M. P. Waller, D. E. Hibbs, and R. J. Clarke Cholesterol Effect on the Dipole Potential of Lipid Membranes Biophys. J., June 1, 2006; 90(11): 4060 - 4070. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Hartel, M. L. Fanani, and B. Maggio Shape Transitions and Lattice Structuring of Ceramide-Enriched Domains Generated by Sphingomyelinase in Lipid Monolayers Biophys. J., January 1, 2005; 88(1): 287 - 304. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. L. Brockman, M. M. Momsen, R. E. Brown, L. He, J. Chun, H.-S. Byun, and R. Bittman The 4,5-Double Bond of Ceramide Regulates Its Dipole Potential, Elastic Properties, and Packing Behavior Biophys. J., September 1, 2004; 87(3): 1722 - 1731. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. L. Fanani, S. Hartel, R. G. Oliveira, and B. Maggio Bidirectional Control of Sphingomyelinase Activity and Surface Topography in Lipid Monolayers Biophys. J., December 1, 2002; 83(6): 3416 - 3424. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Asawakarn, J. Cladera, and P. O'Shea Effects of the Membrane Dipole Potential on the Interaction of Saquinavir with Phospholipid Membranes and Plasma Membrane Receptors of Caco-2 Cells J. Biol. Chem., October 12, 2001; 276(42): 38457 - 38463. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Journal of Biological Chemistry |
| Molecular and Cellular Proteomics | ASBMB Today |