Soft perforation of planar bilayer lipid membranes of dipalmitoylphosphatidylcholine at the temperature of the phase transition from the liquid crystalline to the gel state

Eur Biophys J. 2005 Mar;34(2):155-62. doi: 10.1007/s00249-004-0438-8. Epub 2004 Oct 5.

Abstract

In contrast to the widely used method of electroporation, the method of soft perforation of lipid bilayers is proposed. It is based on the structural rearrangement of the lipid bilayer formed from disaturated phospholipids at the temperature of the phase transition from the liquid crystalline state to the gel state. This allows us to obtain a lipid pore population without the use of a strong electric field. It is shown that the planar lipid bilayer membrane (pBLM) formed from dipalmitoylphosphatidylcholine in 1 M LiCl aqueous solution exhibits the appearance of up to 50 lipid pores per 1 mm(2) of membrane surface, with an average single pore conductivity of 31 +/- 13 nS. The estimation of a single pore radius carried out with water-soluble poly(ethylene glycol)s (PEGs) showed that the average pore radius ranged between 1.0-1.7 nm. It was found experimentally that PEG-1450, PEG-2000, and PEG-3350 should be in a position to block the single pore conductivity completely, while PEG-6000 fully restored the ionic conductivity. The similarity of these PEG effects to ionic conductivity in protein pores makes it possible to suggest that the partition of the PEG molecules between the pore and the bulk solution does not depend on the nature of the chemical groups located in the pore wall.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallization / methods
  • Dimyristoylphosphatidylcholine / chemistry*
  • Electric Conductivity
  • Gels / chemistry
  • Lipid Bilayers / chemistry*
  • Membrane Fluidity*
  • Membrane Potentials
  • Molecular Conformation
  • Permeability
  • Phase Transition
  • Polyethylene Glycols / chemistry*
  • Porosity
  • Solutions

Substances

  • Gels
  • Lipid Bilayers
  • Solutions
  • Polyethylene Glycols
  • Dimyristoylphosphatidylcholine