Related Experiment Video
Updated: May 2, 2026

10:08
Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy
Published on: October 24, 2017
11.4K
Shapes of vesicles encapsulating two aqueous phases.
1College of Materials Science and Engineering, Hunan University, Changsha, 410082, China. kunkunguo@hnu.edu.cn.
Soft Matter
|March 21, 2014
Summary
This study explores two-phase vesicles using polymer and membrane theories. Reduced polymer entropy drives shape changes, altering vesicle morphology and phase diagrams.
Area of Science:
- Soft matter physics
- Biophysics
- Polymer science
Background:
- Vesicles are crucial in biological systems and nanotechnology.
- Understanding the behavior of multi-phase vesicles is key to controlling their properties.
- Polymer-induced phase separation and shape changes in vesicles are complex phenomena.
Purpose of the Study:
- To theoretically investigate vesicles containing two aqueous polymer phases.
- To analyze the impact of polymer concentration and membrane interactions on vesicle shape.
- To map the morphological phase diagrams of these complex vesicles.
Main Methods:
- Utilized Helfrich curvature elasticity theory for fluid membranes.
- Employed self-consistent field theory for polymer behavior.
- Calculated spatial polymer distributions and vesicle shapes.
Main Results:
- Achieved stable vesicle shapes with two distinct polymer phases.
- Demonstrated that reduced polymer conformational entropy influences vesicle shape.
- Identified shifts in phase boundaries (oblate-prolate, oblate-stomatocyte) with altered reduced volume.
- Observed oblates occupying a larger reduced volume range compared to neat vesicles.
Conclusions:
- Polymer properties and membrane interactions significantly dictate vesicle morphology.
- Inhomogeneous entropic pressures arising from polymer confinement drive shape transformations.
- Morphological phase diagrams provide insights into vesicle behavior under varying conditions.
More Related Videos
Related Concept Videos
Pinching-off of Coated Vesicles
3.1K
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...
3.1K
Vesicular Tubular Clusters
2.4K
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...
2.4K
SNAREs and Membrane Fusion
10.4K
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...
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...
10.4K
Intralumenal Vesicles and Multivesicular Bodies
4.0K
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...
4.0K
COP Coated Vesicles
12.6K
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...
12.6K
Fusion of Secretory Vesicles with the Plasma Membrane
15.9K
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...
15.9K

