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Cholesterol modifies the short-range repulsive interactions between phosphatidylcholine membranes.

Publication ,  Journal Article
McIntosh, TJ; Magid, AD; Simon, SA
Published in: Biochemistry
January 10, 1989

Pressure versus distance relationships have been obtained for egg phosphatidylcholine bilayers containing a range of cholesterol concentrations. Water was removed from between adjacent bilayers by the application of osmotic pressures in the range of 0.4-2600 atm (4 x 10(5)-2.6 x 10(9) dyn/cm2), and the distance between adjacent bilayers was obtained by Fourier analysis of X-ray diffraction data. For applied pressures up to about 50 atm and bilayer surface separations of 15-5 A, the incorporation of up to equimolar cholesterol has little influence on plots of pressure versus bilayer separation. However, for the higher applied pressures, cholesterol reduces the interbilayer separation distance by an amount that depends on the cholesterol concentration in the bilayer. For example, the incorporation of equimolar cholesterol reduces the distance between bilayers by as much as 6 A at an applied pressure of 2600 atm. At this applied pressure, electron density profiles show that the high-density head-group peaks from apposing bilayers have merged. This indicates that equimolar concentrations of cholesterol spread the lipid molecules apart in the plane of the bilayer enough to allow the phosphatidylcholine head groups from apposing bilayers to interpenetrate as the bilayers are squeezed together. All of these X-ray and pressure-distance data indicate that, by reducing the volume fraction of phospholipid head groups, cholesterol markedly reduces the steric repulsion between apposing bilayers but has a much smaller effect on the sum of the longer ranged repulsive hydration and fluctuation pressures. Increasing concentrations of cholesterol monotonically increase the dipole potential of egg phosphatidylcholine monolayers, from 415 mV with no cholesterol to 493 mV with equimolar cholesterol.(ABSTRACT TRUNCATED AT 250 WORDS)

Duke Scholars

Published In

Biochemistry

DOI

ISSN

0006-2960

Publication Date

January 10, 1989

Volume

28

Issue

1

Start / End Page

17 / 25

Location

United States

Related Subject Headings

  • X-Ray Diffraction
  • Phosphatidylcholines
  • Osmotic Pressure
  • Lipid Bilayers
  • Cholesterol
  • Biochemistry & Molecular Biology
  • 3404 Medicinal and biomolecular chemistry
  • 3205 Medical biochemistry and metabolomics
  • 3101 Biochemistry and cell biology
  • 1101 Medical Biochemistry and Metabolomics
 

Citation

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McIntosh, T. J., Magid, A. D., & Simon, S. A. (1989). Cholesterol modifies the short-range repulsive interactions between phosphatidylcholine membranes. Biochemistry, 28(1), 17–25. https://doi.org/10.1021/bi00427a004
McIntosh, T. J., A. D. Magid, and S. A. Simon. “Cholesterol modifies the short-range repulsive interactions between phosphatidylcholine membranes.Biochemistry 28, no. 1 (January 10, 1989): 17–25. https://doi.org/10.1021/bi00427a004.
McIntosh TJ, Magid AD, Simon SA. Cholesterol modifies the short-range repulsive interactions between phosphatidylcholine membranes. Biochemistry. 1989 Jan 10;28(1):17–25.
McIntosh, T. J., et al. “Cholesterol modifies the short-range repulsive interactions between phosphatidylcholine membranes.Biochemistry, vol. 28, no. 1, Jan. 1989, pp. 17–25. Pubmed, doi:10.1021/bi00427a004.
McIntosh TJ, Magid AD, Simon SA. Cholesterol modifies the short-range repulsive interactions between phosphatidylcholine membranes. Biochemistry. 1989 Jan 10;28(1):17–25.
Journal cover image

Published In

Biochemistry

DOI

ISSN

0006-2960

Publication Date

January 10, 1989

Volume

28

Issue

1

Start / End Page

17 / 25

Location

United States

Related Subject Headings

  • X-Ray Diffraction
  • Phosphatidylcholines
  • Osmotic Pressure
  • Lipid Bilayers
  • Cholesterol
  • Biochemistry & Molecular Biology
  • 3404 Medicinal and biomolecular chemistry
  • 3205 Medical biochemistry and metabolomics
  • 3101 Biochemistry and cell biology
  • 1101 Medical Biochemistry and Metabolomics