Abstract
Supported lipid bilayer (SLB) membranes are key elements to mimic membrane interfaces on a planar surface. Here, we demonstrate that azobenzene photolipids (azo-PC) form fluid, homogeneous SLBs. Diffusion properties of azo-PC within SLBs were probed by fluorescence microscopy and fluorescence recovery after photobleaching. At ambient conditions, we find that the trans-to-cis isomerization causes an increase of the diffusion constant by a factor of two. Simultaneous excitation with two wavelengths and variable intensities furthermore allows to adjust the diffusion constant D continuously. X-ray reflectometry and small-angle scattering measurements reveal that membrane photoisomerization results in a bilayer thickness reduction of similar to 0.4 nm (or 10%). While thermally induced back-switching is not observed, we find that the trans bilayer fluidity is increasing with higher temperatures. This change in diffusion constant is accompanied by a red-shift in the absorption spectra. Based on these results, we suggest that the reduced diffusivity of trans-azo-PC is controlled by intermolecular interactions that also give rise to H-aggregate formation in bilayer membranes.
| Item Type: | Journal article |
|---|---|
| Faculties: | Physics |
| Research Centers: | Center for NanoScience (CENS) |
| Subjects: | 500 Science > 530 Physics 500 Science > 500 Science |
| ISSN: | 0743-7463 |
| Language: | English |
| Item ID: | 89089 |
| Date Deposited: | 25. Jan 2022 09:28 |
| Last Modified: | 25. Jan 2022 09:28 |
