| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Biophysical Journal 61: 786-799 (1992)
© 1992 the Biophysical Society
Department of Neurobiology, Duke University Medical Center, Durham, North Carolina 27710.
ABSTRACT
The effects of the cholesterol analog 5 alpha-cholestan-3 beta-ol-6-one (6-ketocholestanol) on bilayer structure, bilayer cohesive properties, and interbilayer repulsive pressures have been studied by a combination of x-ray diffraction, pipette aspiration, and dipole potential experiments. It is found that 6-ketocholestanol, which has a similar structure to cholesterol except with a keto moiety at the 6 position of the B ring, has quite different effects than cholesterol on bilayer organization and cohesive properties. Unlike cholesterol, 6-ketocholestanol does not appreciably modify the thickness of liquid-crystalline egg phosphatidylcholine (EPC) bilayers, and causes a much smaller increase in bilayer compressibility modulus than does cholesterol. These data imply that 6-ketocholestanol has both its hydroxyl and keto moieties situated near the water-hydrocarbon interface, thus making its orientation in the bilayer different from cholesterol's. The addition of equimolar 6-ketocholestanol into EPC bilayers increases the magnitude, but not the decay length, of the exponentially decaying repulsive hydration pressure between adjacent bilayers. Incorporation of equimolar 6-ketocholestanol into EPC monolayers increases the dipole potential by approximately 300 mV. These data are consistent with our previous observation that the magnitude of the hydration pressure is proportional to the square of the dipole potential. These results mean that 6-ketocholestanol, despite its location in the bilayer hydrocarbon region, approximately 10 A from the physical edge of the bilayer, modifies the organization of interlamellar water. We argue that the incorporation of 6-ketocholestanol into EPC bilayers increases the hydration pressure, at least in part, by increasing the electric field strength in the polar head group region.
This article has been cited by other articles:
![]() |
D. H. Kim and J. A. Frangos Effects of Amyloid {beta}-Peptides on the Lysis Tension of Lipid Bilayer Vesicles Containing Oxysterols Biophys. J., July 15, 2008; 95(2): 620 - 628. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Jin, A. C. Millard, J. P. Wuskell, X. Dong, D. Wu, H. A. Clark, and L. M. Loew Characterization and Application of a New Optical Probe for Membrane Lipid Domains Biophys. J., April 1, 2006; 90(7): 2563 - 2575. [Abstract] [Full Text] [PDF] |
||||
![]() |
X.-M. Li, M. M. Momsen, H. L. Brockman, and R. E. Brown Sterol Structure and Sphingomyelin Acyl Chain Length Modulate Lateral Packing Elasticity and Detergent Solubility in Model Membranes Biophys. J., December 1, 2003; 85(6): 3788 - 3801. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. S. Klymchenko, G. Duportail, Y. Mely, and A. P. Demchenko Ultrasensitive two-color fluorescence probes for dipole potential in phospholipid membranes PNAS, September 30, 2003; 100(20): 11219 - 11224. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. J. Schroepfer Jr. Oxysterols: Modulators of Cholesterol Metabolism and Other Processes Physiol Rev, January 1, 2000; 80(1): 361 - 554. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Cladera, I. Martin, J.-M. Ruysschaert, and P. O'Shea Characterization of the Sequence of Interactions of the Fusion Domain of the Simian Immunodeficiency Virus with Membranes. ROLE OF THE MEMBRANE DIPOLE POTENTIAL J. Biol. Chem., October 15, 1999; 274(42): 29951 - 29959. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |