Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2008 Jul;15(7):675-83.
doi: 10.1038/nsmb.1455.

Mechanics of membrane fusion

Leonid V Chernomordik  1 , Michael M Kozlov
Affiliations
Review

Mechanics of membrane fusion

Leonid V Chernomordik et al. Nat Struct Mol Biol. 2008 Jul.

Abstract

Diverse membrane fusion reactions in biology involve close contact between two lipid bilayers, followed by the local distortion of the individual bilayers and reformation into a single, merged membrane. We consider the structures and energies of the fusion intermediates identified in experimental and theoretical work on protein-free lipid bilayers. On the basis of this analysis, we then discuss the conserved fusion-through-hemifusion pathway of merger between biological membranes and propose that the entire progression, from the close juxtaposition of membrane bilayers to the expansion of a fusion pore, is controlled by protein-generated membrane stresses.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Fusion-through hemifusion pathway of lipid bilayer fusion. (a) (i) Pre-fusion contact. (ii) A point-like membrane protrusion minimizes the energy of the hydration repulsion between the proximal leaflets of the membranes coming into immediate contact. (iii) A hemifusion stalk with proximal leaflets fused and distal leaflets unfused. (iv) Stalk expansion yields the hemifusion diaphragm. (v) A fusion pore forms either in the hemifusion diaphragm bilayer or directly from the stalk. Dashed lines show the boundaries of the hydrophobic surfaces of monolayers. (b) Different lipids spontaneously form monolayers of different curvatures and, thus, demonstrate different effective molecular shapes. Monolayers formed by inverted cone–shaped lysophosphatidylcholine (LPC) and by cone-shaped phosphatidylethanolamine (PE) and diacylglycerol (DAG) bulge in the direction of the polar heads and in the direction of the hydrocarbon chains, respectively. Cylindrical phosphatidylcholine (PC) forms an almost flat monolayer.
Figure 2
Figure 2
The stalk is the key intermediate in most of the theoretical models developed with the continuous and the simulation approaches. (a) Stalk structure computed by analysis of bending, splay and tilt of the lipid molecules in the membrane monolayers with the elastic model (continuous approach). (b) Stalk structure computed by the self-consistent field model (continuous approach). Light regions indicate the areas of head groups of the bilayer. (c) Stalk structure ‘observed’ by molecular dynamics simulation of the fusion between liposomes composed of dipalmitoyl phosphatidylcholine and palmitic acid using an atomistically detailed model. Water molecules (gray) and head group atoms of the lipids are depicted as spheres; tails are shown as bonds, with gray used to distinguish water molecules originating on different sides of the fusing membranes. The coloring also distinguishes between lipid molecules coming from different leaflets of the bilayers: dipalmitoyl phosphatidylcholine molecules in the inner or outer leaflets (green and purple), and palmitic acid in the inner or outer leaflets (cyan or magenta, respectively).
Figure 3
Figure 3
Hypothetical pathway of biological fusion powered by protein-generated membrane stresses. (a) In the initial state, apposing membrane bilayers are separated by at least a 10–20 nm gap. The contact might involve protein fusogens themselves or be mediated by specialized tethering molecules (green shapes). (b) Fusion proteins induce local bending of membrane bilayer(s) and establish very close contact between the membranes. Generation of large membrane curvature might involve shallow insertion of amphiphilic protein domains (red shapes) into the membrane,. The highly stressed and protein-depleted tops of the bilayer bulges are primed for hemifusion and pore opening,,,. (c) Activated fusion proteins (blue shapes) might drive fusion pore expansion by assembling into an interconnected protein coat surrounding the fusion site. This membrane-associated fusion coat has an intrinsic curvature opposite to that of the budding and fission coats. The coat, bending toward its preferred curvature, deforms the underlying membrane and produces tension that drives fusion and expands the fusion pore.
See this image and copyright information in PMC

Similar articles

See all similar articles

Cited by

See all "Cited by" articles

References

    1. Duelli D, Lazebnik Y. Cell-to-cell fusion as a link between viruses and cancer. Nat Rev Cancer. 2007;7:968–976. - PubMed
    1. Sapir A, Avinoam O, Podbilewicz B, Chernomordik LV. Viral and developmental cell fusion mechanisms: conservation and divergence. Dev Cell. 2008;14:11–21. - PMC - PubMed
    1. Chen EH, Grote E, Mohler W, Vignery A. Cell-cell fusion. FEBS Lett. 2007;581:2181–2193. - PubMed
    1. Kielian M, Rey FA. Virus membrane-fusion proteins: more than one way to make a hairpin. Nat Rev Microbiol. 2006;4:67–76. - PMC - PubMed
    1. Weissenhorn W, Hinz A, Gaudin Y. Virus membrane fusion. FEBS Lett. 2007;581:2150–2155. - PMC - PubMed

Publication types