Toward Cell Membrane Biomimetic Lipidic Cubic Phases: A High-Throughput Exploration of Lipid Compositional Space.

SAXS cholesterol cubosome high throughput lipidic cubic phase lyotropic liquid crystals molecular modeling monoolein nanoparticles phospholipids self-assembly

Journal

ACS applied bio materials
ISSN: 2576-6422
Titre abrégé: ACS Appl Bio Mater
Pays: United States
ID NLM: 101729147

Informations de publication

Date de publication:
22 Jan 2019
Historique:
entrez: 12 1 2022
pubmed: 22 1 2019
medline: 22 1 2019
Statut: ppublish

Résumé

The bicontinuous lipidic cubic phase (LCP), which is based on the fundamental structure of the lipid bilayer, is increasingly used in a range of applications including drug delivery, in meso crystallization of membrane proteins, biosensors, and biofuel cells. The majority of LCPs investigated to date have been formulated from a single lipid or a combination of two lipids in water. Such systems lack tunability, with only a narrow range of lattice parameters adopted. In addition, the lipid bilayer of these materials lacks the complexity of natural cell membranes, which are composed of hundreds of different lipids and which may be essential to retaining the functionality of proteins embedded within them. In this work, we investigate the phase behavior of quaternary lipid-water systems consisting of three different lipids (monoolein-cholesterol-phospholipid) and water using a combination of experimental and simulation techniques. This study provides a large library of lipidic materials with bilayer compositions, which more effectively mimic the native cell membrane and significantly increased tunability based on nanostructural parameters such as lattice parameter, aqueous channel size, and bilayer thickness. Importantly, the library contained several extremely swollen cubic phases with a maximum lattice parameter of up to 342.5 Å. Many of these cubic phases were successfully dispersed into highly swollen cubosomes. The swollen cubic phases described in this article contain only uncharged lipids and are therefore particularly useful for applications with a high salt concentration, including encapsulation of larger therapeutic proteins and peptides for in vivo delivery, or for the crystallization of large membrane proteins such as GPCRs.(1).

Identifiants

pubmed: 35016341
doi: 10.1021/acsabm.8b00539
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

182-195

Auteurs

Sampa Sarkar (S)

School of Science, College of Science, Engineering and Health, RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.

Nhiem Tran (N)

School of Science, College of Science, Engineering and Health, RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.

Md Harunur Rashid (MH)

School of Engineering, RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.

Tu C Le (TC)

School of Engineering, RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.

Irene Yarovsky (I)

School of Engineering, RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.

Charlotte E Conn (CE)

School of Science, College of Science, Engineering and Health, RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.

Calum J Drummond (CJ)

School of Science, College of Science, Engineering and Health, RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.

Classifications MeSH