Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

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...
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%...
Diffusion01:12

Diffusion

Diffusion is the passive movement of substances down their concentration gradients—requiring no expenditure of cellular energy. Substances, such as molecules or ions, diffuse from an area of high concentration to an area of low concentration in the cytosol or across membranes. Eventually, the concentration will even out, with the substance moving randomly but causing no net change in concentration. Such a state is called dynamic equilibrium, which is essential for maintaining overall...
Diffusion01:21

Diffusion

Diffusion is a type of passive transport. In passive transport, a substance tends to move from an area of high concentration to an area of low concentration until the concentration is equal across the space. For example, take the diffusion of substances through the air. When someone opens a perfume bottle in a room filled with people, the perfume is at its highest concentration in the bottle and is at its lowest at the edges of the room. The perfume vapor will diffuse, or spread away, from the...
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...
Passive Diffusion: Overview and Kinetics01:17

Passive Diffusion: Overview and Kinetics

Passive diffusion is a critical process that allows small lipophilic drugs to cross the cell membrane along a concentration gradient. This mechanism's efficiency depends on four primary factors: the membrane's surface area, the drug's lipid-water partition coefficient, the concentration gradient, and the membrane's thickness.
When administered orally, drugs establish a substantial concentration gradient between the gastrointestinal (GI) lumen and the bloodstream, expediting their diffusion into...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Interaction between particles with inhomogeneous surface charge distributions: Revisiting the Coulomb fission of dication molecular clusters.

The Journal of chemical physics·2019
Same author

[Structure of amyloid-beta peptides in a complex with model membranes].

Tsitologiia·2015
Same author

High-resolution NMR structure of the antimicrobial peptide protegrin-2 in the presence of DPC micelles.

Journal of biomolecular NMR·2014
Same author

[Objectivization of the choice of the amputation level in patients with lower limb critical ischaemia].

Angiologiia i sosudistaia khirurgiia = Angiology and vascular surgery·2013
Same author

[Intra-operative histochemical detection of vitalized muscular tissue during lower limb amputation for chronic critical ischemia].

Khirurgiia·2011
Same author

[Effectiveness of new diagnostic drug Diaskintest in children for tuberculosis diagnostic].

Problemy tuberkuleza i boleznei legkikh·2009

Related Experiment Video

Updated: Jun 7, 2026

Fluorescence Recovery after Merging a Droplet to Measure the Two-dimensional Diffusion of a Phospholipid Monolayer
07:54

Fluorescence Recovery after Merging a Droplet to Measure the Two-dimensional Diffusion of a Phospholipid Monolayer

Published on: October 15, 2015

Lateral diffusion in sphingomyelin bilayers.

A V Filippov1, M A Rudakova, B V Munavirov

  • 1Kazan (Volga Region) Federal University, 18, Kazan 420008, Russia. andfil@ltu.se

Magnetic Resonance in Chemistry : MRC
|October 30, 2010
PubMed
Summary

Sphingomyelin (SM) lipids diffuse slower in cell membranes than similar lipids. Longer acyl chains in sphingomyelin molecules correlate with reduced lateral diffusion, potentially due to molecular protrusion or separation.

More Related Videos

Spot Variation Fluorescence Correlation Spectroscopy for Analysis of Molecular Diffusion at the Plasma Membrane of Living Cells
05:56

Spot Variation Fluorescence Correlation Spectroscopy for Analysis of Molecular Diffusion at the Plasma Membrane of Living Cells

Published on: November 12, 2020

From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope
15:10

From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope

Published on: October 9, 2014

Related Experiment Videos

Last Updated: Jun 7, 2026

Fluorescence Recovery after Merging a Droplet to Measure the Two-dimensional Diffusion of a Phospholipid Monolayer
07:54

Fluorescence Recovery after Merging a Droplet to Measure the Two-dimensional Diffusion of a Phospholipid Monolayer

Published on: October 15, 2015

Spot Variation Fluorescence Correlation Spectroscopy for Analysis of Molecular Diffusion at the Plasma Membrane of Living Cells
05:56

Spot Variation Fluorescence Correlation Spectroscopy for Analysis of Molecular Diffusion at the Plasma Membrane of Living Cells

Published on: November 12, 2020

From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope
15:10

From Fast Fluorescence Imaging to Molecular Diffusion Law on Live Cell Membranes in a Commercial Microscope

Published on: October 9, 2014

Area of Science:

  • Biophysics
  • Lipid Bilayer Dynamics
  • Membrane Biophysics

Background:

  • Sphingomyelin (SM) is a crucial lipid in eukaryotic cell membranes and neuronal tissues.
  • Understanding lipid lateral diffusion is key to comprehending membrane function and organization.

Purpose of the Study:

  • To investigate the lateral diffusion of various sphingomyelins (SMs) in oriented lipid bilayers.
  • To compare the lateral diffusion coefficients (LDCs) of SMs with dipalmitoylphosphatidylcholine (DPPC).
  • To explore the influence of SM molecular structure, particularly acyl chain length, on diffusion.

Main Methods:

  • Pulsed field gradient nuclear magnetic resonance (PFG NMR) was employed to measure LDCs.
  • Experiments were conducted on synthetic palmitoylsphingomyelin (PSM) and natural SMs (egg yolk, bovine brain, bovine milk).
  • Temperature range: 45-60 °C.
  • Analysis of (1)H NMR spectra was used to correlate chain length with LDC.

Main Results:

  • Mean LDCs of SMs were 1.9-fold lower than DPPC, suggesting stronger intermolecular interactions.
  • Natural SMs exhibited complex spin-echo diffusion decay, indicating a distribution of LDC values.
  • This complexity was attributed to broad distributions of hydrocarbon chain lengths in natural SMs.
  • A correlation was confirmed between longer acyl chains and lower LDC values.

Conclusions:

  • Intermolecular interactions significantly influence SM lateral diffusion.
  • Variations in acyl chain length distribution among natural SMs lead to differences in their diffusion.
  • Longer acyl chains likely decrease LDC through mechanisms like protrusion or lateral segregation within bilayers.