Structure and dynamics of lipid monolayers: implications for enzyme catalysed lipolysis

Nat Struct Biol. 1995 May;2(5):395-401. doi: 10.1038/nsb0595-395.

Abstract

We have investigated the role of the substrate on the interfacial activation of lipases by an interdisciplinary study of the structure and dynamics of 1,2-sn dipalmitoylglycerol monolayers at distinct surface pressures. The diglyceride Langmuir film undergoes two phase transitions occurring at 38.3 and 39.8 A2 per molecule. The first transition is unique for diglyceride molecules and is driven by a reorganization of the headgroups causing a change in the hydrophobicity of the oil-water interface. X-ray diffraction studies of different mesophases shows that in the two highest pressure phases, the alkyl chains pack in an hexagonal structure relaxing to a distorted-hexagonal lattice in the lowest pressure phase with the alkyl chains tilted by approximately 14 degrees in a direction close to a nearest neighbour direction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Computer Simulation
  • Diglycerides / chemistry
  • Diglycerides / metabolism
  • Lipase / metabolism*
  • Lipolysis*
  • Membrane Lipids / chemistry*
  • Membrane Lipids / metabolism
  • Models, Chemical
  • Palmitic Acids / chemistry
  • Pressure
  • Substrate Specificity
  • Surface Properties
  • X-Ray Diffraction

Substances

  • Diglycerides
  • Membrane Lipids
  • Palmitic Acids
  • Lipase