» Articles » PMID: 32485905

Continuum Models of Membrane Fusion: Evolution of the Theory

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2020 Jun 4
PMID 32485905
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Starting from fertilization, through tissue growth, hormone secretion, synaptic transmission, and sometimes morbid events of carcinogenesis and viral infections, membrane fusion regulates the whole life of high organisms. Despite that, a lot of fusion processes still lack well-established models and even a list of main actors. A merger of membranes requires their topological rearrangements controlled by elastic properties of a lipid bilayer. That is why continuum models based on theories of membrane elasticity are actively applied for the construction of physical models of membrane fusion. Started from the view on the membrane as a structureless film with postulated geometry of fusion intermediates, they developed along with experimental and computational techniques to a powerful tool for prediction of the whole process with molecular accuracy. In the present review, focusing on fusion processes occurring in eukaryotic cells, we scrutinize the history of these models, their evolution and complication, as well as open questions and remaining theoretical problems. We show that modern approaches in this field allow continuum models of membrane fusion to stand shoulder to shoulder with molecular dynamics simulations, and provide the deepest understanding of this process in multiple biological systems.

Citing Articles

SARS-CoV-2 FP1 Destabilizes Lipid Membranes and Facilitates Pore Formation.

Sumarokova M, Pavlov R, Lavushchenko T, Vasilenko E, Kozhemyakin G, Fedorov O Int J Mol Sci. 2025; 26(2).

PMID: 39859399 PMC: 11765642. DOI: 10.3390/ijms26020686.


Boosting Lipofection Efficiency Through Enhanced Membrane Fusion Mechanisms.

Pavlov R, Akimov S, Dashinimaev E, Bashkirov P Int J Mol Sci. 2025; 25(24.

PMID: 39769303 PMC: 11677079. DOI: 10.3390/ijms252413540.


Cell surface crowding is a tunable biophysical barrier to cell-cell fusion.

Lee D, Oster L, Son S, Fletcher D bioRxiv. 2024; .

PMID: 39713336 PMC: 11661186. DOI: 10.1101/2024.12.12.628283.


Lipid Selectivity of Membrane Action of the Fragments of Fusion Peptides of Marburg and Ebola Viruses.

Shekunov E, Efimova S, Kever L, Ishmanov T, Ostroumova O Int J Mol Sci. 2024; 25(18).

PMID: 39337389 PMC: 11432738. DOI: 10.3390/ijms25189901.


Cell-cell fusion in cancer: The next cancer hallmark?.

Shultes P, Weaver D, Tadele D, Barker-Clarke R, Scott J Int J Biochem Cell Biol. 2024; 175():106649.

PMID: 39186970 PMC: 11752790. DOI: 10.1016/j.biocel.2024.106649.


References
1.
Efrat A, Chernomordik L, Kozlov M . Point-like protrusion as a prestalk intermediate in membrane fusion pathway. Biophys J. 2007; 92(8):L61-3. PMC: 1831690. DOI: 10.1529/biophysj.106.103341. View

2.
Chen E, Grote E, Mohler W, Vignery A . Cell-cell fusion. FEBS Lett. 2007; 581(11):2181-93. DOI: 10.1016/j.febslet.2007.03.033. View

3.
Harmandaris V, Deserno M . A novel method for measuring the bending rigidity of model lipid membranes by simulating tethers. J Chem Phys. 2006; 125(20):204905. DOI: 10.1063/1.2372761. View

4.
Sampath S, Sampath S, Millay D . Myoblast fusion confusion: the resolution begins. Skelet Muscle. 2018; 8(1):3. PMC: 5793351. DOI: 10.1186/s13395-017-0149-3. View

5.
Risselada H, Kutzner C, Grubmuller H . Caught in the act: visualization of SNARE-mediated fusion events in molecular detail. Chembiochem. 2011; 12(7):1049-55. DOI: 10.1002/cbic.201100020. View