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Mechanisms of Membrane Domain Formation00:59

Mechanisms of Membrane Domain Formation

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Different physical properties of lipids and proteins allow them to localize and form distinct islands or domains in the membrane. Some membrane domains are formed due to protein-protein interactions, whereas others are formed due to the presence of specific lipids such as sphingolipids and sterols—for example, large proteins, such as bacteriorhodopsin, aggregate and create distinct domains.
Another mechanism for membrane domain formation involves membrane proteins interacting with...
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Mechanisms of Membrane-bending01:15

Mechanisms of Membrane-bending

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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...
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Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

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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...
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Clathrin Coated Vesicles01:12

Clathrin Coated Vesicles

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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...
8.6K
Membrane Domains01:18

Membrane Domains

6.8K
The membrane domains concentrate specific lipids and proteins at one place within the membrane, which helps in cell signaling, adhesion, and other critical cellular processes. These domains can differ in size, composition, function, and lifespan.
Protein Domains
The membrane comprises a group of distinct proteins responsible for carrying out a cell's specific function. For example, the plasma membrane of the human sperm, or a single germ cell, contains a unique set of proteins in the...
6.8K
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

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Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
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Related Experiment Video

Updated: Dec 7, 2025

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

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Active particles induce large shape deformations in giant lipid vesicles.

Hanumantha Rao Vutukuri1, Masoud Hoore2, Clara Abaurrea-Velasco2

  • 1Soft Materials, Department of Materials, ETH Zürich, Zürich, Switzerland. h.r.vutukuri@mat.ethz.ch.

Nature
|October 1, 2020
PubMed
Summary
This summary is machine-generated.

Self-propelled particles inside giant unilamellar vesicles create complex, non-equilibrium shapes and active membrane fluctuations. This research models cell membrane dynamics and could inform the design of artificial cells and soft robots.

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Preparation of Giant Vesicles Encapsulating Microspheres by Centrifugation of a Water-in-oil Emulsion
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Last Updated: Dec 7, 2025

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

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Area of Science:

  • Biophysics
  • Soft Matter Physics
  • Cellular Mechanics

Background:

  • Biological cells actively sculpt internal membranes for sensing and environmental interaction.
  • Pathogenic bacteria utilize internal forces to deform host cell membranes for invasion.
  • Giant unilamellar vesicles serve as minimal models for cellular membranes, but creating internal active forces remains a challenge.

Purpose of the Study:

  • To investigate how self-propelled particles within giant unilamellar vesicles induce membrane deformations and shape changes.
  • To explore the relationship between internal active forces and emergent vesicle morphologies.
  • To develop a minimal model system capable of dynamic membrane sculpting.

Main Methods:

  • Experimental observation of membrane response to self-phoretic Janus microswimmers using confocal microscopy.
  • Langevin dynamics simulations of active Brownian particles within membrane shells (dynamically triangulated surfaces).
  • Quantification of dynamic membrane changes and shape transformations.

Main Results:

  • Self-propelled particles induce diverse non-equilibrium shapes and active membrane fluctuations.
  • Low to moderate particle concentrations lead to tether-like protrusions and dendritic structures.
  • High particle concentrations result in globally deformed vesicle shapes.
  • A state diagram is generated predicting shape outcomes based on internal force conditions.

Conclusions:

  • Internal active forces from enclosed particles can drive significant, controllable membrane deformations.
  • The study provides a framework for understanding active membrane dynamics in minimal systems.
  • Findings may advance the design of synthetic cells and micro-scale soft robotics.