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Related Concept Videos

SNAREs and Membrane Fusion01:43

SNAREs and Membrane Fusion

Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
Fusion of Secretory Vesicles with the Plasma Membrane01:26

Fusion of Secretory Vesicles with the Plasma Membrane

Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
Vesicular Tubular Clusters01:45

Vesicular Tubular Clusters

After budding out from the ER membrane, some COPII vesicles lose their coat and fuse with one another to form larger vesicles and interconnected tubules called vesicular tubular clusters or VTCs. These clusters constitute a compartment at the ER-Golgi interface known as ERGIC (Endoplasmic Reticulum Golgi Intermediate Compartment). The ERGIC is a mobile membrane-bound cargo transport system that sorts proteins secreted from ER and delivers them to the Golgi.
With the help of motor proteins such...
Intralumenal Vesicles and Multivesicular Bodies01:38

Intralumenal Vesicles and Multivesicular Bodies

Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
Clathrin Coated Vesicles01:12

Clathrin Coated Vesicles

Clathrin-coated vesicles use endocytosis to transport receptors and lysosomal hydrolases from the Golgi to the lysosome in the late secretory pathway. Clathrin-mediated endocytosis was the first described endocytic process, and Clathrin-coated vesicles remain one of the most well-studied transport vesicles. The molecular machinery that generates clathrin-coated vesicles comprises over 50 proteins that precisely coordinate vesicle formation. Cell surface receptors concentrated in indented sites...

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Related Experiment Video

Updated: Jul 15, 2026

SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy
10:58

SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy

Published on: August 24, 2016

Lipid-based mechanisms for vesicle fission.

A J Markvoort1, A F Smeijers, K Pieterse

  • 1Departments of Biomedical Engineering and Chemical Engineering, TU Eindhoven, Postbus 513, 5600 MB Eindhoven, The Netherlands. A.J.Markvoort@tue.nl

The Journal of Physical Chemistry. B
|April 12, 2007
PubMed
Summary

This study explores lipid vesicle fission, revealing two distinct pathways driven by lipid asymmetry. The second pathway, involving monolayer composition differences, requires less lipid variation for successful fission compared to the first.

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A Model Membrane Platform for Reconstituting Mitochondrial Membrane Dynamics
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Last Updated: Jul 15, 2026

SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy
10:58

SNARE-mediated Fusion of Single Proteoliposomes with Tethered Supported Bilayers in a Microfluidic Flow Cell Monitored by Polarized TIRF Microscopy

Published on: August 24, 2016

Obtention of Giant Unilamellar Hybrid Vesicles by Electroformation and Measurement of their Mechanical Properties by Micropipette Aspiration
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A Model Membrane Platform for Reconstituting Mitochondrial Membrane Dynamics
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Area of Science:

  • Biophysics
  • Cell Biology
  • Materials Science

Background:

  • Lipid vesicles undergo shape transformations like fusion and fission, crucial for biological processes.
  • Understanding these topological changes is key to deciphering cellular functions and developing new biomaterials.

Purpose of the Study:

  • Investigate two distinct mechanisms of lipid vesicle fission.
  • Analyze the conditions required for complete fission via molecular dynamics simulations.
  • Compare the efficiency and outcomes of different fission pathways.

Main Methods:

  • Utilized molecular dynamics simulations with a coarse-grained lipid model.
  • Examined two primary fission routes based on membrane lipid asymmetry.
  • Analyzed lipid distribution and phase separation within membrane leaflets and monolayers.

Main Results:

  • Identified two distinct lipid vesicle fission pathways driven by membrane asymmetry.
  • Demonstrated that monolayer composition differences (second pathway) require less lipid variation for fission than leaflet phase separation (first pathway).
  • Observed significantly different lipid compositions in the resulting vesicles for each pathway.

Conclusions:

  • Lipid asymmetry dictates distinct vesicle fission mechanisms and outcomes.
  • The monolayer composition-driven pathway is more efficient, requiring subtler lipid differences for fission.
  • Fission and fusion processes exhibit fundamental differences in lipid vesicle dynamics.