Volume 249, 2024

Water–lipid interface in lipidic mesophases with excess water

Abstract

This study investigates the influence of excess water on the lipidic mesophase during the phase transition from diamond cubic phase (Pn[3 with combining macron]m) to reverse hexagonal phase (HII). Using a combination of small angle X-ray scattering (SAXS), broadband dielectric spectroscopy (BDS), and Fourier transform infrared (FTIR) techniques, we explore the dynamics of lipids and their interaction with water during phase transition. Our BDS results reveal three relaxation processes originating from lipids, all of which exhibit a kink during the phase transition. With the excess water, these processes accelerate due to the plasticizing effect of water. Additionally, our results demonstrate that the headgroups in the HII phase are more densely packed than those in the Pn[3 with combining macron]m phase, which agrees with the FTIR results. Meanwhile, we investigate the influence of excess water on the lipid headgroups, the H-bond network of water, the lipid tail, and the interface carbonyl group between the head and tail of the lipid molecule. The results indicate that excess water permeates the lipid interface and forms additional hydrogen bonds with the carbonyl groups. As a result, the headgroups are more flexible in a lipidic mesophase with excess water than those in mesophases without excess water.

Graphical abstract: Water–lipid interface in lipidic mesophases with excess water

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
11 Jun 2023
Accepted
27 Jun 2023
First published
29 Jun 2023
This article is Open Access
Creative Commons BY license

Faraday Discuss., 2024,249, 469-484

Water–lipid interface in lipidic mesophases with excess water

Y. Yao, S. Catalini, P. Foggi and R. Mezzenga, Faraday Discuss., 2024, 249, 469 DOI: 10.1039/D3FD00118K

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