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Membrane Fluidity01:23

Membrane Fluidity

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.Fatty acids tails of phospholipids can be either saturated or...
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...
Protein Diffusion in the Membrane01:24

Protein Diffusion in the Membrane

Proteins show rotational as well as lateral diffusion across the membrane. The lateral diffusion of proteins was confirmed through the cell fusion experiment where mouse and human cells were fused, resulting in hybrid cells. When the human and mouse cells fused, the specific membrane proteins on human and mouse cells were marked with the red and green-fluorescent markers, respectively. Initially, the red and green fluorescence was located on the respective hemisphere of the cell. As time...
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...
Cellular Membranes and Drug Transport01:24

Cellular Membranes and Drug Transport

Drugs must traverse multiple biological barriers, such as multi-layered skin, single-layered intestinal epithelium, and the plasma membrane, to reach their target sites within the body. The plasma membrane, a highly structured composite of phospholipids, carbohydrates, and proteins, is the cell's protective boundary, facilitating selective substance exchange.
Phospholipids arrange themselves into a bilayer, with hydrophilic heads oriented outward and hydrophobic tails facing inward.
Bacterial Translocation and Protein Secretion01:26

Bacterial Translocation and Protein Secretion

Bacterial protein secretion involves translocation systems to ensure proteins reach their designated locations, including the plasma membrane, periplasm, outer membrane, or the external environment. These translocation systems are vital for bacterial physiology, supporting processes like membrane assembly, enzymatic activity in the periplasm, and interactions with the external environment. The division of labor between Sec and Tat pathways ensures efficiency in handling proteins with diverse...

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Activated scramblase and inhibited aminophospholipid translocase cause phosphatidylserine exposure in a distinct platelet fraction.

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Related Experiment Video

Updated: Jul 9, 2026

Measuring Peptide Translocation into Large Unilamellar Vesicles
12:27

Measuring Peptide Translocation into Large Unilamellar Vesicles

Published on: January 27, 2012

Lipid translocation across the plasma membrane of mammalian cells.

E M Bevers1, P Comfurius, D W Dekkers

  • 1Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands. em.bevers@bioch.unimaas.nl

Biochimica Et Biophysica Acta
|August 14, 1999
PubMed
Summary

Cell membrane lipid asymmetry is maintained by specific protein transporters. Impaired function, like in Scott syndrome, disrupts this balance, leading to lipid scrambling and phosphatidylserine exposure.

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Last Updated: Jul 9, 2026

Measuring Peptide Translocation into Large Unilamellar Vesicles
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Published on: March 21, 2025

Area of Science:

  • Cell Biology
  • Biochemistry
  • Membrane Biophysics

Background:

  • The plasma membrane regulates cellular communication and function through its specific lipid and protein composition.
  • Maintaining lipid asymmetry between the two membrane leaflets is crucial for cellular processes.
  • The mechanisms governing transbilayer lipid distribution are not fully elucidated.

Purpose of the Study:

  • To review the known mechanisms and transporters involved in maintaining plasma membrane lipid asymmetry.
  • To discuss the roles of aminophospholipid translocase, floppase, and scramblase in lipid transport.
  • To highlight the physiological significance of lipid asymmetry, particularly in relation to Scott syndrome and apoptosis.

Main Methods:

  • Review of existing literature on membrane lipid transport proteins.
  • Discussion of the functional characteristics of aminophospholipid translocase, floppase, and scramblase.
  • Analysis of the consequences of impaired lipid transport, using Scott syndrome as a case study.

Main Results:

  • Identified three key players in transbilayer lipid distribution: aminophospholipid translocase, floppase, and scramblase.
  • Demonstrated that coordinated action of translocase and floppase maintains asymmetry in quiescent cells.
  • Showed that scramblase activation and translocase inhibition lead to lipid asymmetry collapse and phosphatidylserine exposure.

Conclusions:

  • Plasma membrane lipid asymmetry is actively regulated by specific protein transporters.
  • Dysfunctional lipid scrambling, as seen in Scott syndrome, impairs this regulation and has clinical implications.
  • Phosphatidylserine exposure during apoptosis involves the interplay between scramblase activation and translocase inhibition.