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Related Experiment Video

Updated: Jul 14, 2026

Lipid-Protein Membrane Structure-Function Characterization using Droplet Interface Bilayers
10:27

Lipid-Protein Membrane Structure-Function Characterization using Droplet Interface Bilayers

Published on: June 12, 2026

Decrease of elastic moduli of DOPC bilayers induced by a macrolide antibiotic, azithromycin.

N Fa1, L Lins, P J Courtoy

  • 1Université Catholique de Louvain, Unité de Pharmacologie Cellulaire et Moléculaire, Avenue E. Mounier 73, Bt 7370, B-1200 Brussels, Belgium.

Biochimica Et Biophysica Acta
|June 1, 2007
PubMed
Summary

The antibiotic azithromycin alters the elastic properties of lipid bilayers, decreasing their cohesion. This drug-induced change in membrane elasticity influences membrane deformation and drug-membrane interactions, impacting cellular pharmacology.

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Multifunctional, Micropipette-based Method for Incorporation And Stimulation of Bacterial Mechanosensitive Ion Channels in Droplet Interface Bilayers
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Multifunctional, Micropipette-based Method for Incorporation And Stimulation of Bacterial Mechanosensitive Ion Channels in Droplet Interface Bilayers

Published on: November 19, 2015

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Last Updated: Jul 14, 2026

Lipid-Protein Membrane Structure-Function Characterization using Droplet Interface Bilayers
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Published on: June 12, 2026

Multifunctional, Micropipette-based Method for Incorporation And Stimulation of Bacterial Mechanosensitive Ion Channels in Droplet Interface Bilayers
09:54

Multifunctional, Micropipette-based Method for Incorporation And Stimulation of Bacterial Mechanosensitive Ion Channels in Droplet Interface Bilayers

Published on: November 19, 2015

Area of Science:

  • Biophysics
  • Membrane Biophysics
  • Pharmacology

Background:

  • Elastic properties of membrane bilayers are crucial for their function and can be modulated by pharmacological agents.
  • Previous studies indicated azithromycin erodes DPPC domains in DOPC lipid matrices.
  • The effect of azithromycin on DOPC cohesion and membrane elasticity remained uninvestigated.

Purpose of the Study:

  • To investigate the effect of azithromycin on the elastic properties of dioleoylphosphatidylcholine (DOPC) giant unilamellar vesicles (GUVs).
  • To determine how azithromycin influences membrane fluctuations and lipid bilayer cohesion.
  • To provide biophysical evidence for azithromycin's interaction with lipid membranes.

Main Methods:

  • Microcinematographic and morphometric analyses of GUVs.
  • Micropipette aspiration technique to quantify elastic moduli.
  • Computer modeling of azithromycin-DOPC bilayer interactions.

Main Results:

  • Azithromycin addition enhanced lipid membrane fluctuations and disrupted larger GUVs.
  • Azithromycin significantly decreased the bending modulus (k(c)) and apparent area compressibility modulus (K(app)) of DOPC bilayers.
  • Computer modeling predicted azithromycin insertion at the bilayer interface, reducing inter-molecule interactions and increasing molecular surface area.

Conclusions:

  • Azithromycin inserts into the DOPC lipid bilayer, reducing its cohesion and elastic moduli.
  • This alteration in membrane elasticity facilitates the merging of DPPC into the DOPC matrix, consistent with prior observations.
  • These findings provide the first biophysical evidence of an amphiphilic antibiotic altering lipid elastic moduli, with implications for drug-lipid interactions and cellular pharmacology.