Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1989 Jun;86(12):4474–4478. doi: 10.1073/pnas.86.12.4474

Oxygen permeability of phosphatidylcholine--cholesterol membranes.

W K Subczynski 1, J S Hyde 1, A Kusumi 1
PMCID: PMC287292  PMID: 2543978

Abstract

Oxygen transport in phosphatidylcholine-cholesterol membranes has been studied by observing the collision of molecular oxygen with nitroxide radical spin labels placed at various distances from the membrane surface using long-pulse saturation recovery ESR techniques. The collision rate was estimated for tempocholine phosphatidic acid ester, 5-doxylstearic acid, and 16-doxylstearic acid from spin-lattice relaxation times (T1) measured in the presence and absence of molecular oxygen. Profiles of the local oxygen transport parameter across the membrane were obtained as a function of cholesterol mol fraction and temperature in L-alpha-dimyristoylphosphatidylcholine ([ Myr2]PtdCho) and L-alpha-dioleoylphosphatidylcholine ([ Ole2]PtdCho) membranes. Membrane oxygen permeability coefficients were estimated from oxygen transport parameter profiles. At approximately 30 degrees C, the oxygen permeability coefficients in the presence and absence of 50 mol % cholesterol are 22.7 and 125.2 cm/s, respectively, for [Myr2]PtdCho membranes, and 54.7 and 114.2 cm/s, respectively, for [Ole2]PtdCho membranes (compared with 60-80 cm/s for water layers with the same thicknesses as the membranes). The major results in the liquid-crystalline phase are as follows: (i) In the absence of cholesterol, membranes are not barriers to oxygen transport. (ii) Addition of 50 mol % cholesterol decreases oxygen permeability by a factor of approximately 5 and approximately 2.5 in [Myr2]PtdCho and [Ole2]PtdCho membranes, respectively. The resistance to oxygen transport is located in and near the polar headgroup regions in the membrane. (iii) Cholesterol increases oxygen transport in the central regions of [Ole2]PtdCho membranes.

Full text

PDF
4474

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Coin J. T., Olson J. S. The rate of oxygen uptake by human red blood cells. J Biol Chem. 1979 Feb 25;254(4):1178–1190. [PubMed] [Google Scholar]
  2. Cornell B. A., Separovic F. Membrane thickness and acyl chain length. Biochim Biophys Acta. 1983 Aug 24;733(1):189–193. doi: 10.1016/0005-2736(83)90106-2. [DOI] [PubMed] [Google Scholar]
  3. Diamond J. M., Katz Y. Interpretation of nonelectrolyte partition coefficients between dimyristoyl lecithin and water. J Membr Biol. 1974;17(2):121–154. doi: 10.1007/BF01870176. [DOI] [PubMed] [Google Scholar]
  4. Dix J. A., Kivelson D., Diamond J. M. Molecular motion of small nonelectrolyte molecules in lecithin bilayers. J Membr Biol. 1978 Jun 9;40(4):315–342. doi: 10.1007/BF01874162. [DOI] [PubMed] [Google Scholar]
  5. Franks N. P., Lieb W. R. The structure of lipid bilayers and the effects of general anaesthetics. An x-ray and neutron diffraction study. J Mol Biol. 1979 Oct 9;133(4):469–500. doi: 10.1016/0022-2836(79)90403-0. [DOI] [PubMed] [Google Scholar]
  6. Huxley V. H., Kutchai H. Effect of diffusion boundary layers on the initial uptake of O2 by red cells. Theory versus experiment. Microvasc Res. 1983 Jul;26(1):89–107. doi: 10.1016/0026-2862(83)90058-4. [DOI] [PubMed] [Google Scholar]
  7. Huxley V. H., Kutchai H. The effect of the red cell membrane and a diffusion boundary layer on the rate of oxygen uptake by human erythrocytes. J Physiol. 1981 Jul;316:75–83. doi: 10.1113/jphysiol.1981.sp013773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Janiak M. J., Small D. M., Shipley G. G. Nature of the Thermal pretransition of synthetic phospholipids: dimyristolyl- and dipalmitoyllecithin. Biochemistry. 1976 Oct 19;15(21):4575–4580. doi: 10.1021/bi00666a005. [DOI] [PubMed] [Google Scholar]
  9. Janiak M. J., Small D. M., Shipley G. G. Temperature and compositional dependence of the structure of hydrated dimyristoyl lecithin. J Biol Chem. 1979 Jul 10;254(13):6068–6078. [PubMed] [Google Scholar]
  10. Kusumi A., Subczynski W. K., Hyde J. S. Oxygen transport parameter in membranes as deduced by saturation recovery measurements of spin-lattice relaxation times of spin labels. Proc Natl Acad Sci U S A. 1982 Mar;79(6):1854–1858. doi: 10.1073/pnas.79.6.1854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kusumi A., Subczynski W. K., Pasenkiewicz-Gierula M., Hyde J. S., Merkle H. Spin-label studies on phosphatidylcholine-cholesterol membranes: effects of alkyl chain length and unsaturation in the fluid phase. Biochim Biophys Acta. 1986 Jan 29;854(2):307–317. doi: 10.1016/0005-2736(86)90124-0. [DOI] [PubMed] [Google Scholar]
  12. Levine Y. K., Wilkins M. H. Structure of oriented lipid bilayers. Nat New Biol. 1971 Mar 17;230(11):69–72. doi: 10.1038/newbio230069a0. [DOI] [PubMed] [Google Scholar]
  13. Lis L. J., McAlister M., Fuller N., Rand R. P., Parsegian V. A. Interactions between neutral phospholipid bilayer membranes. Biophys J. 1982 Mar;37(3):657–665. [PMC free article] [PubMed] [Google Scholar]
  14. McIntosh T. J. The effect of cholesterol on the structure of phosphatidylcholine bilayers. Biochim Biophys Acta. 1978 Oct 19;513(1):43–58. doi: 10.1016/0005-2736(78)90110-4. [DOI] [PubMed] [Google Scholar]
  15. Merkle H., Subczynski W. K., Kusumi A. Dynamic fluorescence quenching studies on lipid mobilities in phosphatidylcholine-cholesterol membranes. Biochim Biophys Acta. 1987 Feb 26;897(2):238–248. doi: 10.1016/0005-2736(87)90420-2. [DOI] [PubMed] [Google Scholar]
  16. Nagle J. F., Wilkinson D. A. Lecithin bilayers. Density measurement and molecular interactions. Biophys J. 1978 Aug;23(2):159–175. doi: 10.1016/S0006-3495(78)85441-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Presti F. T., Chan S. I. Cholesterol-phospholipid interaction in membranes. 1. Cholestane spin-label studies of phase behavior of cholesterol-phospholipid liposomes. Biochemistry. 1982 Aug 3;21(16):3821–3830. doi: 10.1021/bi00259a016. [DOI] [PubMed] [Google Scholar]
  18. Recktenwald D. J., McConnell H. M. Phase equilibria in binary mixtures of phosphatidylcholine and cholesterol. Biochemistry. 1981 Jul 21;20(15):4505–4510. doi: 10.1021/bi00518a042. [DOI] [PubMed] [Google Scholar]
  19. Sanson A., Ptak M., Rigaud J. L., Gary-Bobo C. M. An ESR study of the anchoring of spin-labeled stearic acid in lecithin multilayers. Chem Phys Lipids. 1976 Nov;17(4):435–444. doi: 10.1016/0009-3084(76)90045-1. [DOI] [PubMed] [Google Scholar]
  20. Subczynski W. K., Hyde J. S. Concentration of oxygen in lipid bilayers using a spin-label method. Biophys J. 1983 Mar;41(3):283–286. doi: 10.1016/S0006-3495(83)84439-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Subczynski W. K., Hyde J. S. Diffusion of oxygen in water and hydrocarbons using an electron spin resonance spin-label technique. Biophys J. 1984 Apr;45(4):743–748. doi: 10.1016/S0006-3495(84)84217-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Subczynski W. K., Hyde J. S. The diffusion-concentration product of oxygen in lipid bilayers using the spin-label T1 method. Biochim Biophys Acta. 1981 May 6;643(2):283–291. [PubMed] [Google Scholar]
  23. Träuble H., Eibl H. Electrostatic effects on lipid phase transitions: membrane structure and ionic environment. Proc Natl Acad Sci U S A. 1974 Jan;71(1):214–219. doi: 10.1073/pnas.71.1.214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Yin J. J., Pasenkiewicz-Gierula M., Hyde J. S. Lateral diffusion of lipids in membranes by pulse saturation recovery electron spin resonance. Proc Natl Acad Sci U S A. 1987 Feb;84(4):964–968. doi: 10.1073/pnas.84.4.964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Zaccai G., Büldt G., Seelig A., Seelig J. Neutron diffraction studies on phosphatidylcholine model membranes. II. Chain conformation and segmental disorder. J Mol Biol. 1979 Nov 15;134(4):693–706. doi: 10.1016/0022-2836(79)90480-7. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES