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Liposomes, Exosomes, and Virosomes: From Modeling Complex
Membrane Processes to Medical Diagnostics and Drug Delivery
Poster Abstracts
81
23-POS
Board 12
Light-Triggered Morphological Transformations in Giant Vesicles
Vasil Georgiev
1
, David Bléger
2
, Andrea Grafmüller
1
, Stefan Hecht
2
, Rumiana Dimova
1
.
1
Max Planck Institute of Colloids and Interfaces, Potsdam, Brandenburg, Germany,
2
Humboldt
University, Berlin, Berlin, Germany.
Regulation of the lipid membrane structure and morphology are critical for many cellular
processes such as the fission-fusion sequence in vesicular transport or endo- and exocytosis. A
well-known membrane mimetic system for exploring such cellular processes is giant unilamellar
vesicles (GUVs). Photosensitive molecules offer a way to modulate the membrane morphology.
Here, we studied the behavior of GUVs in the presence of two photosensitive molecules,
tetrafluoroazobenzene (F-azo) and azobenzene-trimethylammonium-bromide (azoTAB). Upon
irradiation with light (green or UV and blue), the F-azo molecules undergo reversible trans-cis
isomerization [Bléger et al. JACS 134:20597-20600, 2012]. UV and blue light irradiation of the
vesicles mixed with F-azo induce reversible morphological transformations such as budding and
bud readsorption. The molecule partitioning and orientation in the membrane was probed with
molecular dynamics simulations. The energy gain of insertion and the barrier for flipping suggest
that F-azo partitions in the membrane and that the observed GUV morphological transitions
result from the F-azo isomerization. The associated area increase in the GUVs was measured via
vesicle electrodeformation for two different F-azo concentrations. The influence of molecule
isomerization on phase separated vesicles was also examined. The appearance of liquid-
disordered domains within the preexisting liquid ordered phase was observed. Differently from
the action of F-azo molecules, under UV irradiation, azoTAB molecules cause the GUVs to
rupture. A potential application of such system includes the development of drug delivery
systems with light-triggered release of solutes. These results suggest that the photosensitive
molecules provide us with a handle to modulate the membrane morphology and stability.
We acknowledge S. Santer (Potsdam University) for the azoTAB molecules and IMPRS for the
financial support.