Skip to main content
Log in

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

  • Article
  • Published:
European Biophysics Journal Aims and scope Submit manuscript

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 mm2 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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Antonov VF (1998) Lipid pores: stability and permeability of the membrane (in Russian). Soros Educ J 10:10–17

    Google Scholar 

  • Antonov VF, Petrov VV, Molnar AA, Predvoditelev DA, Ivanov AS (1980) The appearance of single ion channels in unmodified lipid bilayer membrane at the phase transition temperature. Nature 283:585–588

    CAS  PubMed  Google Scholar 

  • Antonov VF, Shevchenko EV, Kozhomkulov ET, Molnar AA, Smirnova EYu (1985) Capacitance and ion currents in BLM from phosphatidic acids in Ca2+ induced phase transition. Biochem Biophys Res Commun 133:1098–1103

    CAS  PubMed  Google Scholar 

  • Antonov VF, Smirnova EYu, Shevchenko EV (1992) Lipid membranes at the phase transition (in Russian). Moscow, Nauka, pp 1–135

  • Antonov VF, Anosov AA, Norik VP, Korepanova EA, Smirnova EYu (2003) Electrical capacitance of lipid bilayer membrane of hydrogenated egg lecithin at the temperature phase transition. Eur Biophys J 32:55–59

    CAS  PubMed  Google Scholar 

  • Boheim G, Hanke W, Eibl H (1980) Lipid phase transition in planar lipid membrane and its effect on carrier- and pore-mediated ion transport. Proc Natl Acad Sci USA 77:3403–3407

    CAS  PubMed  Google Scholar 

  • Chernomordik LV, Sukharev IS, Abidor IG, Chismadzhev YuA (1982) The study of the BLM reversible electrical breakdown mechanism in the presence of UO22+. Bioelectrochem Bioenerg 6:149–165

    Article  Google Scholar 

  • Cunningham BA, Shimotake JE, Tamura-Lis W, Mastran T, Kwok JT, Kaufman JW, Lis LJ (1986) The influence of ion species on phosphatidylcholine bilayer structure and packing. Chem Phys Lipids 39:135–143

    Article  CAS  PubMed  Google Scholar 

  • Eldridge CA, Morowitz HJ (1978) A hydrodynamic theory of ion conductance through ohmic pores. J Theor Biol 73:539–548

    CAS  PubMed  Google Scholar 

  • Evans E, Kwok R (1982) Mechanical calorimetry of large dimyristoylphosphatidylcholine vesicles in the phase transition region. Biochemistry 21:4874–4879

    CAS  PubMed  Google Scholar 

  • Freeman SA, Wang MA, Weaver JC (1994) Theory of electroporation of planar bilayer membranes: predictions of aqueous area, change in capacitance and pore-pore separation. Biophys J 67:42–56

    CAS  PubMed  Google Scholar 

  • Gennis R (1989) Biomembranes. Molecular structure and function. Springer, Berlin, Heidelberg, New York

  • Glaser RW, Leikin SL, Chernomordik LV, Pastushenko VF, Sokirko AV (1988) Reversible electrical breakdown of lipid bilayers: formation and evolution of pores. Biochim Biophys Acta 940:275–287

    Article  CAS  PubMed  Google Scholar 

  • Jacobson K, Papahadjopoulos D (1975) Phase transitions and phase separations in phospholipid membranes induced by changes in temperature, pH and concentration of bivalent ions. Biochemistry 14:152–161

    Article  CAS  PubMed  Google Scholar 

  • Kraayenhof R, Sterk GJ, Harro W, Wong FS, Krab K, Epand RM (1996) Monovalent cations differentially affect membrane surface properties and membrane curvature, as revealed by fluorescent probes and dynamic light scattering. Biochim Biophys Acta 1282:293–302

    Article  CAS  PubMed  Google Scholar 

  • Krasilnikov OV (2001) Sizing channels with polymers. In: Kasianowicz JJ, Kellermayer MSZ, Deamer DV (eds) Structure and dynamics of confined polymers. Kluwer, Dordrecht, The Netherlands, pp 73–91

  • Lee RC, Hannig J (2001) Membrane biology and biophysics. Surgical Res 25:297–305

    Google Scholar 

  • Levitt DG (1975) General continuum analysis of transport through pores. II. Nonuniform pores. Biophys J 15:553–563

    CAS  PubMed  Google Scholar 

  • Marra J, Israelashwili J (1985) Direct measurements of forces between phosphatidylcholine and phosphatidylethanolamine bilayers in aqueous electrolyte solutions. Biochemistry 24:4608–4618

    CAS  PubMed  Google Scholar 

  • Mueller P, Rudin D, Tien H, Wescott W (1962) Reconstruction of cell membrane structure in vitro and its transformation into an excitable system. Nature 194:979–980

    CAS  PubMed  Google Scholar 

  • Petrov AC, Mitov AD, Derzhanski AJ (1982) Edge energy and pore stability. In: Bata I (ed) Advances in liquid crystal research and applications, vol 2. Pergamon, Oxford, UK, pp 695–737

  • Rostovtseva TK, Nesterovich EM, Bezrukov SM (2002) Partitioning of differently sized poly(ethylene)glycols into OMPF porin. Biophys J 82:160–169

    CAS  PubMed  Google Scholar 

  • Wilhelm C, Winterhalter M, Zimmermann U, Benz R (1993) Kinetics of pore size during irreversible electrical breakdown of lipid bilayer membranes. Biophys J 64:121–128

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank Prof. G. N. Berestovskij for helpful and stimulating discussions. This work was supported partially by a grant from the Russian Fund for Basic Research.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Valerij F. Antonov.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Antonov, V.F., Anosov, A.A., Norik, V.P. et al. 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 34, 155–162 (2005). https://doi.org/10.1007/s00249-004-0438-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00249-004-0438-8

Keywords

Navigation