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Related Concept Videos

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.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
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.
With the help of motor proteins such...
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...
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.
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Synthesis of Compound Giant Unilamellar Vesicles: A Biomimetic Model of Nucleate Cells
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Model system of self-reproducing vesicles.

Yuka Sakuma1, Masayuki Imai

  • 1Department of Physics, Ochanomizu University, Bunkyo, Tokyo 112-8610, Japan.

Physical Review Letters
|December 21, 2011
PubMed
Summary

Researchers created a model for self-reproducing vesicles, a key step towards artificial life. This system uses lipid shape changes and temperature cycling to achieve budding-type reproduction without needing new membrane synthesis.

Area of Science:

  • Origin of Life Research
  • Supramolecular Chemistry
  • Systems Chemistry

Background:

  • Autopoiesis, or self-reproduction, is fundamental for understanding the origin of life.
  • Creating artificial self-reproducing systems is a major challenge in chemical biology.
  • Previous models often require complex synthesis pathways for membrane components.

Purpose of the Study:

  • To develop a simplified model for self-reproducing vesicle systems.
  • To demonstrate vesicle self-reproduction without de novo membrane synthesis.
  • To investigate the role of lipid shape and phase transitions in vesicle dynamics.

Main Methods:

  • Constructed model vesicles using a mixture of cylinder- and inverse-cone-shaped lipids.
  • Utilized temperature cycling to induce vesicle formation and expulsion of internal structures.

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  • Varied vesicle composition to observe changes in the reproduction pathway.
  • Main Results:

    • Successfully formed inclusion vesicles within mother vesicles.
    • Demonstrated expulsion of inclusion vesicles via temperature cycling.
    • Observed a budding-type self-reproduction pathway dependent on vesicle composition.
    • Identified coupling between lipid main-chain transitions and vesicle shape changes as a key mechanism.

    Conclusions:

    • A functional, simplified model for vesicle self-reproduction was established.
    • Lipid shape and phase transitions are critical for driving budding-type reproduction.
    • This work provides a foundational step towards engineering more complex autopoietic systems.