Eur. Phys. J. E (2013) 36: 77
https://doi.org/10.1140/epje/i2013-13077-0

Regular Article

Influence of charge density on bilayer bending rigidity in lipid vesicles: A combined dynamic light scattering and neutron spin-echo study

¹⁹⁸⁹⁰ Helmholtz Zentrum Berlin, Hahn-Meitner Platz 1, 14109, Berlin, Germany
²⁹⁸⁹⁰ Institut Laue-Langevin, B.P. 156, 38042, Grenoble, France

^* e-mail: beate-annette.bruening@helmholtz-berlin.de

Received: 2 August 2012
Revised: 18 December 2012
Accepted: 20 December 2012
Published online: 17 July 2013

Abstract

We report a combined dynamic light scattering and neutron spin-echo study on vesicles composed of the uncharged stabilizing lipid 1,2-dimyristoyl-sn-glycero-3-phosphatidylcholine (DMPC) and the cationic lipid 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP). Mechanical properties of a model membrane and thus the corresponding bilayer undulation dynamics can be specifically tuned by changing its composition through lipid headgroup or acyl chain properties. We compare the undulation dynamics in lipid vesicles composed of DMPC/DOTAP to vesicles composed of a mixture of the uncharged helper lipid DMPC with the also uncharged reference lipid 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC). We have performed dynamic light scattering on the lipid mixtures to investigate changes in lipid vesicle size and the corresponding center-of-mass diffusion. We study lipid translational diffusion in the membrane plane and local bilayer undulations using neutron spin-echo spectroscopy, on two distinct time scales, namely around 25 ns and around 150 ns. Finally, we calculate the respective bilayer bending rigidities κ for both types of lipid vesicles. We find that on the local length scale inserting lipid headgroup charge into the membrane influences the bilayer undulation dynamics and bilayer bending rigidity κ less than inserting lipid acyl chain unsaturation: We observe a bilayer softening with increasing inhomogenity of the lipid mixture, which could be caused by a hydrophobic mismatch between the acyl chains of the respective lipid components, causing a lateral phase segregation (domain formation) in the membrane plane.