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Photolipid Bilayer Permeability is Controlled by Transient Pore Formation.

Stefanie D PritzlPatrick UrbanAlexander PrasselspergerDavid B KonradJames Allen FrankDirk H TraunerTheobald Lohmüller
Published in: Langmuir : the ACS journal of surfaces and colloids (2020)
Controlling the release or uptake of (bio-) molecules and drugs from liposomes is critically important for a range of applications in bioengineering, synthetic biology, and drug delivery. In this paper, we report how the reversible photoswitching of synthetic lipid bilayer membranes made from azobenzene-containing phosphatidylcholine (azo-PC) molecules (photolipids) leads to increased membrane permeability. We show that cell-sized, giant unilamellar vesicles (GUVs) prepared from photolipids display leakage of fluorescent dyes after irradiation with UV-A and visible light. Langmuir-Blodgett and patch-clamp measurements show that the permeability is the result of transient pore formation. By comparing the trans-to-cis and cis-to-trans isomerization process, we find that this pore formation is the result of area fluctuations and a change of the area cross-section between both photolipid isomers.
Keyphrases
  • drug delivery
  • visible light
  • endothelial cells
  • cerebral ischemia
  • quantum dots
  • cancer therapy
  • cell therapy
  • aqueous solution
  • brain injury
  • bone marrow