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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.
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Membrane fluidity is explained by the fluid mosaic model of the cell membrane, which describes the plasma membrane structure as a mosaic of components—including phospholipids, cholesterol, proteins, and carbohydrates—that gives the membrane a fluid character.
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Cell membranes are composed of phospholipids, proteins, and carbohydrates loosely attached to one another through chemical interactions. Molecules are generally able to move about in the plane of the membrane, giving the membrane its flexible nature called fluidity. Two other features of the membrane contribute to membrane fluidity: the chemical structure of the phospholipids and the presence of cholesterol in the membrane.
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Scientists identified the plasma membrane in the 1890s and its principal chemical components (lipids and proteins) by 1915. The model for plasma membrane structure, proposed in 1935 by Hugh Davson and James Danielli, was the first model to be widely accepted in the scientific community. The model was based on the plasma membrane's "railroad track" appearance in early electron micrographs. Davson and Danielli theorized that the plasma membrane's structure resembled a sandwich...
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A key characteristic of life is the ability to separate the external environment from the internal space. To do this, cells have evolved semi-permeable membranes that regulate the passage of biological molecules. Additionally, the cell membrane defines a cell’s shape and interactions with the external environment. Eukaryotic cell membranes also serve to compartmentalize the internal space into organelles, including the endomembrane structures of the nucleus, endoplasmic reticulum and...
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A cell's plasma membrane demarcates the cell's borders and determines the nature of its interaction with the environment. Cells exclude certain substances, take in others, and excrete some others in controlled quantities. The plasma membrane must be flexible to allow certain cells, such as red and white blood cells, to change their shape while passing through narrow capillaries. These are the more obvious plasma membrane functions. In addition, the plasma membrane's surface carries...
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Programmable Coacervate-Membrane Interactions Direct Internal and Collective Organization in Membranized Protocells.

Vincent Mukwaya1, Xiaolei Yu1, Shuhan Xiong1

  • 1State Key Laboratory of Metal Matrix Composites, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai, P.R. China.

Angewandte Chemie (International Ed. in English)
|March 16, 2026
PubMed
Summary
This summary is machine-generated.

Researchers developed polysaccharidosomes (P-somes), robust protocells that mimic cellular organization. This platform enables programmable control over coacervate-membrane interactions and collective behaviors in synthetic systems.

Keywords:
liquid–liquid phase separationmembranized protocellspolyanion‐induced reconfigurationpolysaccharidosomessynthetic cortex

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Area of Science:

  • Biomimetic engineering
  • Synthetic biology
  • Cellular organization

Background:

  • Eukaryotic cells utilize membraneless organelles that interact with the plasma membrane and cortex.
  • Cytoskeletal coupling and membrane biochemistry regulate organelle positioning, wetting, and function.
  • Recreating adaptive, cortex-mediated control in synthetic systems is challenging.

Purpose of the Study:

  • To introduce a synthetic chassis for programmable coacervate-membrane coupling.
  • To develop mechanically robust protocells with interfacial programmability.
  • To achieve fine control over coacervate wetting, morphology, and spatial organization.

Main Methods:

  • Introduction of polysaccharidosomes (P-somes) as semipermeable, mechanically robust protocells.
  • Establishment of a cortex-like protein layer on the inner membrane leaflet via template-directed assembly.
  • In situ protein succinylation for tuning surface charge and coacervate-membrane wetting.
  • Systematic variation of membrane building blocks and uptake of external DNA for regulation.

Main Results:

  • Demonstrated precise tuning of surface charge and coacervate-membrane wetting through protein succinylation.
  • Achieved fine control over coacervate wetting, morphology, and spatial organization.
  • Showcased DNA-mediated regulation of coacervate behavior, leading to tissue-like clustering or nucleus-like droplet formation.

Conclusions:

  • The developed platform integrates mechanical resilience with chemical programmability.
  • This framework offers a scalable route to constructing membranized protocells with self-organizing interiors.
  • Emergent collective behaviors were observed in the synthetic protocell system.