» Articles » PMID: 19129198

Preparation and Properties of Asymmetric Vesicles That Mimic Cell Membranes: Effect Upon Lipid Raft Formation and Transmembrane Helix Orientation

Overview
Journal J Biol Chem
Specialty Biochemistry
Date 2009 Jan 9
PMID 19129198
Citations 96
Authors
Affiliations
Soon will be listed here.
Abstract

A methyl-beta-cyclodextrin-induced lipid exchange technique was devised to prepare small unilamellar vesicles with stable asymmetric lipid compositions. Asymmetric vesicles that mimic biological membranes were prepared with sphingomyelin (SM) or SM mixed with 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPC) as the predominant lipids in the outer leaflet and dioleoylphosphatidylcholine (DOPC), POPC, 1-palmitoyl-2-oleoyl-phosphatidyl-L-serine (POPS), or POPS mixed with 1-palmitoyl-2-oleoyl-phosphatidylethanolamine (POPE) in the inner leaflet. Fluorescence-based assays were developed to confirm lipid asymmetry. Cholesterol was introduced into these vesicles using a second methyl-beta-cyclodextrin exchange step. In asymmetric vesicles composed of SM outside, DOPC inside (SMo/DOPCi) or SM outside, 2:1 mol:mol POPE:POPS inside (SMo/2:1 POPE:POPSi) the outer leaflet SM formed an ordered state with a thermal stability similar to that in pure SM vesicles and significantly greater than that in symmetric vesicles with the same overall lipid composition. Analogous behavior was observed in vesicles containing cholesterol. This shows that an asymmetric lipid distribution like that in eukaryotic plasma membranes can be conducive to ordered domain (raft) formation. Furthermore asymmetric vesicles containing approximately 25 mol % cholesterol formed ordered domains more thermally stable than those in asymmetric vesicles lacking cholesterol, showing that the crucial ability of cholesterol to stabilize ordered domain formation is likely to contribute to ordered domain formation in cell membranes. Additional studies demonstrated that hydrophobic helix orientation is affected by lipid asymmetry with asymmetry favoring formation of the transmembrane configuration. The ability to form asymmetric vesicles represents an important improvement in model membrane studies and should find many applications in the future.

Citing Articles

Probing SARS-CoV-2 membrane binding peptide via single-molecule AFM-based force spectroscopy.

Zhang Q, Rosa R, Ray A, Durlet K, Dorrazehi G, Bernardi R Nat Commun. 2025; 16(1):6.

PMID: 39747000 PMC: 11696146. DOI: 10.1038/s41467-024-55358-9.


Engineering Phosphatidylserine Containing Asymmetric Giant Unilamellar Vesicles.

McDonough J, Paratore T, Ketelhohn H, DeCilio B, Ross A, Gericke A Membranes (Basel). 2024; 14(9).

PMID: 39330522 PMC: 11433827. DOI: 10.3390/membranes14090181.


Biomimetic Lipid Raft: Domain Stability and Interaction with Physiologically Active Molecules.

Shimokawa N, Takagi M Adv Exp Med Biol. 2024; 1461:15-32.

PMID: 39289271 DOI: 10.1007/978-981-97-4584-5_2.


MαCD-based plasma membrane outer leaflet lipid exchange in mammalian cells to study insulin receptor activity.

Suresh P, London E Methods Enzymol. 2024; 700():485-507.

PMID: 38971611 PMC: 11748235. DOI: 10.1016/bs.mie.2024.03.027.


MemPrep, a new technology for isolating organellar membranes provides fingerprints of lipid bilayer stress.

Reinhard J, Starke L, Klose C, Haberkant P, Hammaren H, Stein F EMBO J. 2024; 43(8):1653-1685.

PMID: 38491296 PMC: 11021466. DOI: 10.1038/s44318-024-00063-y.


References
1.
Antignani A, Youle R . How do Bax and Bak lead to permeabilization of the outer mitochondrial membrane?. Curr Opin Cell Biol. 2006; 18(6):685-9. DOI: 10.1016/j.ceb.2006.10.004. View

2.
Lerch-Bader M, Lundin C, Kim H, Nilsson I, von Heijne G . Contribution of positively charged flanking residues to the insertion of transmembrane helices into the endoplasmic reticulum. Proc Natl Acad Sci U S A. 2008; 105(11):4127-32. PMC: 2393759. DOI: 10.1073/pnas.0711580105. View

3.
Wang T, Leventis R, Silvius J . Fluorescence-based evaluation of the partitioning of lipids and lipidated peptides into liquid-ordered lipid microdomains: a model for molecular partitioning into "lipid rafts". Biophys J. 2000; 79(2):919-33. PMC: 1300989. DOI: 10.1016/S0006-3495(00)76347-8. View

4.
Huang C, Mason J . Geometric packing constraints in egg phosphatidylcholine vesicles. Proc Natl Acad Sci U S A. 1978; 75(1):308-10. PMC: 411236. DOI: 10.1073/pnas.75.1.308. View

5.
Ren J, Lew S, Wang Z, London E . Transmembrane orientation of hydrophobic alpha-helices is regulated both by the relationship of helix length to bilayer thickness and by the cholesterol concentration. Biochemistry. 1997; 36(33):10213-20. DOI: 10.1021/bi9709295. View