Cited by 240Lipid Membrane Structure and BehaviorCellular transport and secretionCaveolin-1 and cellular processes

Time scales of membrane fusion revealed by direct imaging of vesicle fusion with high temporal resolution

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Haluska, Christopher K., Riske, Karin A., Marchi-Artzner, Valérie, Lehn, Jean-Marie, Lipowsky, Reinhard, Dimova, Rumiana·2006·Proceedings of the National Academy of Sciences

Abstract

Membrane fusion is a vital process of life involved, for example, in cellular secretion via exocytosis, signaling between nerve cells, and virus infection. In both the life sciences and bioengineering, controlled membrane fusion has many possible applications, such as drug delivery, gene transfer, chemical microreactors, or synthesis of nanomaterials. Until now, the fusion dynamics has been elusive because direct observations have been limited to time scales that exceed several milliseconds. Here, the fusion of giant lipid vesicles is induced in a controlled manner and monitored with a temporal resolution of 50 μs. Two different fusion protocols are used that are based on synthetic fusogenic molecules and electroporation. For both protocols, the opening of the fusion necks is very fast, with an average expansion velocity of centimeters per second. This velocity indicates that the initial formation of a single fusion neck can be completed in a few hundred nanoseconds.

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Crossref · 10.1073/pnas.0602766103

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  • This topologically and energetically distinct pathway for membrane fusion is of particular interest because transmembrane potentials, of similar magnitude to those (ca. 0.1 V/nm) leading to electropores in lipid bilayers, may occur naturally across lipid membranes of vesicles and cells.

    “This topologically and energetically distinct pathway for membrane fusion is of particular interest because transmembrane potentials, of similar magnitude to those (ca.0.1V/nm) leading to electropores in lipid bilayers, may occur naturally across lipid membranes of vesicles and cells, as recently demonstrated 8,12 , as well as under external application 9,34 .”

    From Fusion of lipid membranes: an alternative pathway (2026) · cites this paper as [34]

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Authors
Haluska, C. K., Riske, K. A., Marchi-Artzner, V., Lehn, J.-M., Lipowsky, R., & Dimova, R.
Affiliations
  • Max Planck Institute of Colloids and Interfaces (DE)
  • Laboratoire de Chimie des Interactions Moléculaires, Collège de France, 75005 Paris, France
  • Max Planck Society (DE)
Venue
Proceedings of the National Academy of Sciences
Published
2006-10-24
Volume
103
Issue
43
Pages
15841-15846
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2113214821
Cited by
240
References
1
Citations by year
2026: 11 · 2024: 7 · 2023: 10 · 2022: 18 · 2021: 12 · 2020: 10 · 2019: 14 · 2018: 10 · 2017: 21 · 2016: 15 · 2015: 12 · 2014: 19 · 2013: 13 · 2012: 15
FWCI
2.77
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
  • Max Planck Institute for Plasma Physics (submittedVersion)
  • Max Planck Digital Library (submittedVersion)
  • MPG.PuRe (Max Planck Society) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Caveolin-1 and cellular processes
Keywords
membrane fusion, fusion kinetics, giant lipid vesicles, electroporation, high temporal resolution imaging, exocytosis
MeSH terms
Animals, Chickens, Electrons, Ligands, Membrane Fusion, Time Factors

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