Related Experiment Video
Updated: Dec 15, 2025

10:08
Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy
Published on: October 24, 2017
9.5K
Shape Transformations of Vesicles Induced by Their Adhesion to Flat Surfaces
1Institute of Physical Chemistry Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.
ACS Omega
|July 14, 2020
Summary
Lipid vesicles change shape when adhering to surfaces. Researchers determined the stable shapes of these adhered vesicles and discovered new phenomena like budding.
Area of Science:
- Biophysics
- Soft Matter Physics
- Materials Science
Background:
- Lipid vesicles are fundamental in biological systems and nanotechnology.
- Their shape is influenced by membrane properties and external interactions.
- Understanding adhesion-induced shape changes is crucial for various applications.
Purpose of the Study:
- To investigate the shape transformations of lipid vesicles upon adhesion to a flat surface.
- To determine the stability of different vesicle shapes (oblate, prolate, stomatocyte) when adhered.
- To identify novel physical phenomena arising from vesicle-surface adhesion.
Main Methods:
- Utilizing the Helfrich spontaneous curvature model for theoretical calculations.
- Performing simulations for specific values of reduced volume and spontaneous curvature.
- Analyzing the energetic landscape to predict stable vesicle morphologies.
Main Results:
- Established the range of stability for oblate, prolate, and stomatocyte shapes of adhered vesicles.
- Identified critical parameters influencing the shape transitions.
- Observed and reported new phenomena, including adhesion-induced budding.
Conclusions:
- Adhesion to flat surfaces significantly alters lipid vesicle morphology.
- The Helfrich model provides a framework to predict shape stability and transitions.
- Vesicle budding can be triggered by surface adhesion, revealing complex physical behaviors.
More Related Videos
Related Concept Videos
Pinching-off of Coated Vesicles
3.8K
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...
3.8K
Clathrin Coated Vesicles
8.7K
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...
8.7K
Fusion of Secretory Vesicles with the Plasma Membrane
16.3K
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...
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
16.3K
Mechanisms of Membrane-bending
3.2K
The living membranes are flexible due to their fluid mosaic nature; however, their bending into different shapes is an active process regulated by specific lipids and proteins. The membrane bending can be transient as seen in vesicles or stable for a long time as in microvilli. Cells regulate the size, location, and duration of the membrane curvature.
Membrane bending can happen due to intrinsic changes in lipid composition or extrinsic association with different proteins. The proteins involved...
Membrane bending can happen due to intrinsic changes in lipid composition or extrinsic association with different proteins. The proteins involved...
3.2K
COP Coated Vesicles
16.5K
Membrane-enclosed structures called vesicles transport proteins and lipids across the cell. The vesicles derive their cargo from the plasma membrane, Golgi, ER, or endosome. Coated vesicles are spherical, protein-coated carriers with a 50–100 nm diameter that mediate bidirectional transport between the ER and the Golgi. The distribution of proteins between the ER and Golgi complex is dynamic and is maintained by different coated vesicles. Their formation is driven by the assembly of...
16.5K
Vesicular Tubular Clusters
2.9K
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...
With the help of motor proteins such...
2.9K

