Sponge-phase Lipid Droplets as Synthetic Organelles: An Ultrafast Study of Hydrogen Bonding and Interfacial Environments.


Journal

Chemphyschem : a European journal of chemical physics and physical chemistry
ISSN: 1439-7641
Titre abrégé: Chemphyschem
Pays: Germany
ID NLM: 100954211

Informations de publication

Date de publication:
17 10 2023
Historique:
revised: 12 07 2023
received: 19 06 2023
medline: 26 10 2023
pubmed: 24 7 2023
entrez: 24 7 2023
Statut: ppublish

Résumé

Bottom-up design of biomimetic organelles has gained recent attention as a route towards understanding the transition between non-living matter and life. Despite various artificial lipid membranes being developed, the specific relations between lipid structure, composition, interfacial properties, and morphology are not currently understood. Sponge-phase droplets contain dense, nonlamellar lipid bilayer networks that capture the complexities of the endoplasmic reticulum (ER), making them ideal artificial models of such organelles. Here, we combine ultrafast two-dimensional infrared (2D IR) spectroscopy and molecular dynamics simulations to investigate the interfacial H-bond networks in sponge-phase droplets composed of glycolipid and nonionic detergents. In the sponge phase, the interfacial environments are more hydrated and water molecules confined to the nanometer-scale aqueous channels in the sponge phase exhibit dynamics that are significantly slower compared to bulk water. Surfactant configurations and microscopic phase separation play a dominant role in determining membrane curvature and slow dynamics observed in the sponge phase. The studies suggest that H-bond networks within the nanometer-scale channels are disrupted not only by confinement but also by the interactions of surfactants, which extend 1-2 nm from the bilayer surface. The results provide a molecular-level description for controlling phase and morphology in the design of synthetic lipid organelles.

Identifiants

pubmed: 37486881
doi: 10.1002/cphc.202300404
doi:

Substances chimiques

Water 059QF0KO0R
Surface-Active Agents 0
Glycolipids 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202300404

Subventions

Organisme : Department of Defense
Organisme : Multidisciplinary University Research Initiative
ID : W911-NF-13-1-0383
Organisme : Welch Foundation
ID : F-1891

Informations de copyright

© 2023 Wiley-VCH GmbH.

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Auteurs

Cong Xu (C)

Department of Chemistry, The University of Texas at Austin, 105 E. 24th St. Stop A5300, 78712-1224, Austin, TX, USA.

Alessandro Fracassi (A)

Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, Natural Sciences Building 3328, 92093, La Jolla, CA, USA.

Christopher P Baryiames (CP)

Department of Chemistry, The University of Texas at Austin, 105 E. 24th St. Stop A5300, 78712-1224, Austin, TX, USA.

Ahanjit Bhattacharya (A)

Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, Natural Sciences Building 3328, 92093, La Jolla, CA, USA.

Neal K Devaraj (NK)

Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, Natural Sciences Building 3328, 92093, La Jolla, CA, USA.

Carlos R Baiz (CR)

Department of Chemistry, The University of Texas at Austin, 105 E. 24th St. Stop A5300, 78712-1224, Austin, TX, USA.

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