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Related Concept Videos

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...
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...
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...
Assembly of the Lipid Bilayer in the ER01:28

Assembly of the Lipid Bilayer in the ER

Biological membranes are more than just a barrier separating cell cytoplasm from the outside environment. They are highly dynamic and help maintain the integrity and physiological stability of the cells as well as membrane-bound organelles. Membranes also play vital roles in cell-to-cell and intracellular communication.
A large chunk of any biological membrane is composed of phospholipids. These lipids have a heterogeneous distribution across different subcellular organelles and even between...
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...
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...

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Related Experiment Video

Updated: May 20, 2026

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

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Published on: August 24, 2016

Lipid bilayer membrane-triggered presynaptic vesicle assembly.

Gopakumar Gopalakrishnan1, Peter Thostrup, Isabelle Rouiller

  • 1Department of Chemistry, McGill University, 801 Sherbrooke Street West, H3A 2K6 Montreal, Canada.

ACS Chemical Neuroscience
|July 11, 2012
PubMed
Summary

Engineered neural networks require functional synapses. Researchers used spherical supported bilayer lipid membranes (SS-BLMs) as a novel substrate to demonstrate presynaptic vesicle accumulation, advancing artificial synapse development.

Keywords:
Lipid membranesneurodegenerative diseasesneuronsregenerative medicinesupported bilayerssynapse

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Area of Science:

  • Neuroscience
  • Biomaterials Science
  • Bioengineering

Background:

  • Developing in vitro neural networks necessitates the formation of functional synapses on artificial substrates.
  • Spherical supported bilayer lipid membranes (SS-BLMs) offer a promising novel platform for creating artificial synaptic junctions.

Purpose of the Study:

  • To investigate the potential of SS-BLMs as a substrate for demonstrating presynaptic vesicle accumulation.
  • To explore the interactions between neurons and SS-BLMs in the context of in vitro synaptogenesis.

Main Methods:

  • Characterization of SS-BLMs using confocal fluorescence microscopy, cryo-transmission electron microscopy (cryo-TEM), and fluorescence recovery after photobleaching (FRAP).
  • Observation of presynaptic vesicle formation at neuron-SS-BLM contacts via immunocytochemistry and confocal fluorescence microscopy.

Main Results:

  • Demonstrated presynaptic vesicle accumulation at in vitro synaptic junctions formed on SS-BLMs.
  • Identified potential roles for lipid phases, alongside chemical and electrostatic interactions, in neuron-SS-BLM interactions.

Conclusions:

  • SS-BLMs serve as a viable substrate for artificial synapse formation, showing presynaptic vesicle accumulation.
  • The biocompatibility and tunable nature of lipid bilayers make SS-BLMs a valuable tool for neuroengineering and in vivo synaptogenesis research.