Change of motion and localization of cholesterol molecule during L(alpha)-H(II) transition

Biophys J. 1998 Feb;74(2 Pt 1):892-8. doi: 10.1016/S0006-3495(98)74012-3.

Abstract

Formation of the inverted hexagonal (H(II)) phase from the lamellar (L(alpha)) phase of bovine brain-extracted phosphatidylcholine (BBPC) and phosphatidylethanolamine (BBPE) was investigated using 31P-NMR with or without cholesterol. When the ratio of BBPC to BBPE was 1:1, the H(II) formation was observed in the presence of 33 mol% cholesterol (i.e., BBPC:BBPE:cholesterol = 1:1:1) at 47 degrees C. The fraction of the H(II) phase in the BBPC/BBPE/cholesterol system could be controlled by the addition of dioleoylglycerol. The change of molecular motion of cholesterol affected by the H(II) formation was measured at various ratios of the L(alpha) to H(II) phase with the time-resolved fluorescence depolarization method, using dehydroergosterol as a fluorescent probe. It is observed that the motion of cholesterol became vigorous in the mixture state of the L(alpha) and the H(II) phases compared to that in the L(alpha) or the H(II) phase only. These facts show that cholesterol has the strong ability to induce the H(II) phase, probably by special molecular motion, which includes change of its location from the headgroup area to the acyl-chain area.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Chemistry
  • Cattle
  • Cholesterol / chemistry*
  • Diglycerides
  • Fluorescence Polarization
  • Liposomes / chemistry*
  • Models, Molecular
  • Molecular Conformation
  • Nuclear Magnetic Resonance, Biomolecular
  • Phosphatidylcholines / chemistry*
  • Phosphatidylcholines / isolation & purification
  • Phosphatidylethanolamines / chemistry*
  • Phosphatidylethanolamines / isolation & purification
  • Phosphorus
  • Time Factors

Substances

  • Diglycerides
  • Liposomes
  • Phosphatidylcholines
  • Phosphatidylethanolamines
  • Phosphorus
  • Cholesterol
  • diolein