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Related Concept Videos

Asymmetric Lipid Bilayer01:35

Asymmetric Lipid Bilayer

Biological membranes show uneven distribution of different types of lipids in the inner and outer layers, resulting in transverse asymmetric membranes. The treatment of the erythrocyte membrane with the enzyme phospholipase confirmed the asymmetric nature of the lipid bilayer. The enzyme hydrolyzes lipids into fatty acids and hydrophilic groups. The phospholipase acts only on the outer layer of the membrane, while the inner layer remains intact. The phospholipase treatment resulted in 80%...
Fluid Mosaic Model01:19

Fluid Mosaic Model

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 with the analogy of...
Membrane Asymmetry Regulating Transporters01:19

Membrane Asymmetry Regulating Transporters

Enzymes like flippase, floppase, and scramblase transfer phospholipids from one layer to another in the membrane, thereby affecting membrane asymmetry.
Flippase
Eukaryotic flippases are type-IV P-type ATPases or P4-ATPases belonging to P-type ATPase family proteins that are membrane-bound pumps involved in the ATP-mediated transport of ions and molecules across the membrane. Flippases flip specific phospholipids from the outer to the inner leaflet of a membrane. All P4-ATPases have one...
Membrane Fluidity01:26

Membrane Fluidity

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.
Mosaic nature of the membrane
The mosaic characteristic of the membrane helps the plasma membrane remain fluid. The integral proteins and lipids exist as separate but loosely-attached molecules in the membrane. The membrane is a relatively...

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Related Experiment Video

Updated: Jun 17, 2026

Atomic Force Microscopy Imaging and Force Spectroscopy of Supported Lipid Bilayers
10:15

Atomic Force Microscopy Imaging and Force Spectroscopy of Supported Lipid Bilayers

Published on: July 22, 2015

Frustrated phase transformations in supported, interdigitating lipid bilayers.

Babak Sanii1, Alan W Szmodis, Daniel A Bricarello

  • 1Molecular Foundry, Lawrence Berkeley National Lab, Berkeley, California, USA.

The Journal of Physical Chemistry. B
|December 17, 2009
PubMed
Summary
This summary is machine-generated.

Confining a fluorinated phospholipid (F-DPPC) near a surface prevents full gel phase formation. This frustration leads to unusual phase coexistence, impacting lipid bilayer properties and transition temperatures.

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Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy
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Last Updated: Jun 17, 2026

Atomic Force Microscopy Imaging and Force Spectroscopy of Supported Lipid Bilayers
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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

Area of Science:

  • Lipid bilayer thermodynamics and phase transitions
  • Surface confinement effects on lipid organization

Background:

  • Monofluorinated phospholipids (F-DPPC) undergo a fluid to gel phase transition in free bilayers.
  • This transition involves acyl tail ordering, increased molecular area, and decreased bilayer thickness.
  • Confinement near a solid surface introduces constraints on lipid reorganization.

Purpose of the Study:

  • To investigate the effects of surface confinement on the F-DPPC phase transition.
  • To understand how planar topography and constant surface area influence lipid reorganization.
  • To characterize the resulting phase behavior and coexistence.

Main Methods:

  • Utilizing lipid bilayer models with controlled surface confinement.
  • Observing phase transitions under topographical and area constraints.
  • Analyzing lipid organization and phase coexistence using biophysical techniques.

Main Results:

  • Surface confinement limits the formation of the energetically favored interdigitated gel phase.
  • Non-interdigitated lipids experience increased lateral tension due to area constraints.
  • This leads to elevated transition temperatures, supercooling, and vitrification.
  • An unusual phase coexistence of two distinct gel phases is observed.

Conclusions:

  • Frustrated phase transitions in confined lipid bilayers couple dynamics and thermodynamics.
  • Surface constraints alter lipid phase behavior, leading to novel states.
  • Understanding these confined systems is crucial for biomembrane and material science applications.