» Articles » PMID: 32946808

Lateral Heterogeneity and Domain Formation in Cellular Membranes

Overview
Specialty Biochemistry
Date 2020 Sep 18
PMID 32946808
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

As early as the development of the fluid mosaic model for cellular membranes, researchers began observing the telltale signs of lateral heterogeneity. Over the decades this has led to the development of the lipid raft hypothesis and the ensuing controversy that has unfolded, as a result. Here, we review the physical concepts behind domain formation in lipid membranes, both of their structural and dynamic origins. This, then leads into a discussion of coarse-grained, phenomenological approaches that describe the wide range of phases associated with lipid lateral heterogeneity. We use these physical concepts to describe the interaction between raft-lipid species, such as long-chain saturated lipids, sphingomyelin, and cholesterol, and non-raft forming lipids, such as those with short acyl chains or unsaturated fatty acids. While debate has persisted on the biological relevance of lipid domains, recent research, described here, continues to identify biological roles for rafts and new experimental approaches have revealed the existence of lipid domains in living systems. Given the recent progress on both the biological and structural aspects of raft formation, the research area of membrane lateral heterogeneity will not only expand, but will continue to produce exciting results.

Citing Articles

Partitioning into ER membrane microdomains impacts autophagic protein turnover during cellular aging.

Prokisch S, Buttner S Sci Rep. 2024; 14(1):13653.

PMID: 38871812 PMC: 11176346. DOI: 10.1038/s41598-024-64493-8.


Is cholesterol both the lock and key to abnormal transmembrane signals in Autism Spectrum Disorder?.

Lingwood C Lipids Health Dis. 2024; 23(1):114.

PMID: 38643132 PMC: 11032007. DOI: 10.1186/s12944-024-02075-3.


Quantitative Comparison against Experiments Reveals Imperfections in Force Fields' Descriptions of POPC-Cholesterol Interactions.

Javanainen M, Heftberger P, Madsen J, Miettinen M, Pabst G, Ollila O J Chem Theory Comput. 2023; 19(18):6342-6352.

PMID: 37616238 PMC: 10536986. DOI: 10.1021/acs.jctc.3c00648.


Eukaryotic Cell Membranes: Structure, Composition, Research Methods and Computational Modelling.

Zhukov A, Popov V Int J Mol Sci. 2023; 24(13).

PMID: 37446404 PMC: 10342339. DOI: 10.3390/ijms241311226.


Biophysical studies of lipid nanodomains using different physical characterization techniques.

Kinnun J, Scott H, Bolmatov D, Collier C, Charlton T, Katsaras J Biophys J. 2023; 122(6):931-949.

PMID: 36698312 PMC: 10111277. DOI: 10.1016/j.bpj.2023.01.024.


References
1.
Stone M, Shelby S, Nunez M, Wisser K, Veatch S . Protein sorting by lipid phase-like domains supports emergent signaling function in B lymphocyte plasma membranes. Elife. 2017; 6. PMC: 5373823. DOI: 10.7554/eLife.19891. View

2.
Gaus K, Gratton E, Kable E, Jones A, Gelissen I, Kritharides L . Visualizing lipid structure and raft domains in living cells with two-photon microscopy. Proc Natl Acad Sci U S A. 2003; 100(26):15554-9. PMC: 307606. DOI: 10.1073/pnas.2534386100. View

3.
Kucerka N, Nieh M, Katsaras J . Fluid phase lipid areas and bilayer thicknesses of commonly used phosphatidylcholines as a function of temperature. Biochim Biophys Acta. 2011; 1808(11):2761-71. DOI: 10.1016/j.bbamem.2011.07.022. View

4.
Wassall S, Stillwell W . Polyunsaturated fatty acid-cholesterol interactions: domain formation in membranes. Biochim Biophys Acta. 2008; 1788(1):24-32. DOI: 10.1016/j.bbamem.2008.10.011. View

5.
Lavrentovich M, Horsley E, Radja A, Sweeney A, Kamien R . First-order patterning transitions on a sphere as a route to cell morphology. Proc Natl Acad Sci U S A. 2016; 113(19):5189-94. PMC: 4868417. DOI: 10.1073/pnas.1600296113. View