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Related Concept Videos

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...
COP Coated Vesicles00:59

COP Coated Vesicles

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 different...
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...
Overview of Secretory Vesicles01:33

Overview of Secretory Vesicles

Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
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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...
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.
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Updated: Jul 7, 2026

Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy
10:08

Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy

Published on: October 24, 2017

Characterization of DODAB/DPPC vesicles.

Cecília N C Sobral1, Marco A Soto, Ana M Carmona-Ribeiro

  • 1Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, P.O. Box 26077, 05513-970 São Paulo, SP, Brazil.

Chemistry and Physics of Lipids
|February 9, 2008
PubMed
Summary
This summary is machine-generated.

Dioctadecyldimethylammonium bromide (DODAB)/dipalmitoylphosphatidylcholine (DPPC) cationic vesicles show optimal stability at 50% DODAB. This composite formulation enhances colloid stability across various salt concentrations, crucial for biotechnological applications.

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Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy
10:08

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Published on: October 24, 2017

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09:29

Obtention of Giant Unilamellar Hybrid Vesicles by Electroformation and Measurement of their Mechanical Properties by Micropipette Aspiration

Published on: January 19, 2020

Area of Science:

  • Materials Science
  • Colloid and Surface Chemistry
  • Biotechnology

Background:

  • Dioctadecyldimethylammonium bromide (DODAB) and dipalmitoylphosphatidylcholine (DPPC) are key lipids for vesicle formulation.
  • Cationic vesicles are essential for various biotechnological applications.
  • Understanding lipid-bilayer interactions is crucial for vesicle stability.

Purpose of the Study:

  • To characterize DODAB/DPPC cationic vesicles.
  • To investigate the effect of DODAB concentration on vesicle phase behavior and colloid stability.
  • To assess the stability of composite vesicles in different salt concentrations.

Main Methods:

  • Vesicle preparation via vortexing lipid films.
  • Characterization techniques: phase behavior determination, size distribution analysis, zeta-potential measurement, and colloid stability assessment.
  • Evaluation of vesicle stability in varying NaCl concentrations (1, 50, 150mM).

Main Results:

  • Non-monotonic phase behavior observed with increasing DODAB percentage.
  • Maximum mean phase transition temperature and colloid stability achieved at 50% DODAB.
  • Remarkable colloid stability for 50% DODAB/DPPC vesicles in all tested NaCl concentrations, unlike pure DPPC or DODAB vesicles.
  • Vesicle size decreased with increasing DODAB, while zeta-potential remained constant due to reduced counterion binding.

Conclusions:

  • A strong correlation exists between bilayer structure stability and overall colloid stability.
  • The 50% DODAB/DPPC composite vesicles exhibit superior colloid stability compared to pure lipid vesicles.
  • The findings suggest potential for these stable cationic vesicles in diverse biotechnological applications.