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Spontaneous charged lipid transfer between lipid vesicles.
Richens, Joanna L; Tyler, Arwen I I; Barriga, Hanna M G; Bramble, Jonathan P; Law, Robert V; Brooks, Nicholas J; Seddon, John M; Ces, Oscar; O'Shea, Paul.
Afiliação
  • Richens JL; School of Life Sciences, University of Nottingham, Nottingham, United Kingdom.
  • Tyler AII; Food Colloids and Processing Group, School of Food Science and Nutrition, University of Leeds, Leeds, LS2 9JT, United Kingdom.
  • Barriga HMG; Department of Chemistry, Imperial College London, South Kensington, London, SW7 2AZ, United Kingdom.
  • Bramble JP; Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
  • Law RV; Department of Chemistry, Imperial College London, South Kensington, London, SW7 2AZ, United Kingdom.
  • Brooks NJ; Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, V6T 1Z3, Canada.
  • Seddon JM; Department of Chemistry, Imperial College London, South Kensington, London, SW7 2AZ, United Kingdom.
  • Ces O; Department of Chemistry, Imperial College London, South Kensington, London, SW7 2AZ, United Kingdom.
  • O'Shea P; Department of Chemistry, Imperial College London, South Kensington, London, SW7 2AZ, United Kingdom.
Sci Rep ; 7(1): 12606, 2017 10 03.
Article em En | MEDLINE | ID: mdl-28974701
ABSTRACT
An assay to study the spontaneous charged lipid transfer between lipid vesicles is described. A donor/acceptor vesicle system is employed, where neutrally charged acceptor vesicles are fluorescently labelled with the electrostatic membrane probe Fluoresceinphosphatidylethanolamine (FPE). Upon addition of charged donor vesicles, transfer of negatively charged lipid occurs, resulting in a fluorescently detectable change in the membrane potential of the acceptor vesicles. Using this approach we have studied the transfer properties of a range of lipids, varying both the headgroup and the chain length. At the low vesicle concentrations chosen, the transfer follows a first-order process where lipid monomers are transferred presumably through the aqueous solution phase from donor to acceptor vesicle. The rate of transfer decreases with increasing chain length which is consistent with energy models previously reported for lipid monomer vesicle interactions. Our assay improves on existing methods allowing the study of a range of unmodified lipids, continuous monitoring of transfer and simplified experimental procedures.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article