Kinetics of lipid raft formation at lipid monolayer-bilayer junction probed by surface plasmon resonance.

A label-free, non-dispruptive, and real-time analytical device to monitor the dynamic features of biomolecules and their interactions with neighboring molecules is an essential prerequisite for biochip- and diagonostic assays. To explore one of the central questions on the lipid-lipid interactions in the course of the liquid-ordered (lo) domain formation, called rafts, we developed a method of reconstituting continuous but spatially heterogeneous lipid membrane platforms with molayer-bilayer juntions (MBJs) that enable to form the lo domains in a spatiotemporally controlled manner. This allows us to detect the time-lapse dynamics of the lipid-lipid interactions during raft formation and resultant membrane phase changes together with the raft-associated receptor-ligand binding through the surface plasmon resonance (SPR). For cross-validation, using epifluorescence microscopy, we demonstrated the underlying mechanisms for raft formations that the infiltration of cholesterols into the sphingolipid-enriched domains plays a crucial roles in the membrane phase-separation. Our membrane platform, being capable of monitoring dynamic interactions among lipids and performing the systematic optical analysis, will unveil physiological roles of cholesterols in a variety of biological events.

Concept of active parallax barrier on polarizing interlayer for near-viewing autostereoscopic displays.

We proposed a concept of an active parallax barrier using a liquid crystal-on-polarizing interlayer (LPI) for near-viewing autostereoscopic displays. In contrast to a conventional two-panel configuration where two independent panels are stacked together for displaying and parallaxing purposes, a monolithic one-panel architecture was demonstrated with the help of the LPI. The LPI was constructed using a polarizer sheet, one side of which provided the support for the active parallax barrier and the other served as the substrate for the image panel. For the active parallax barrier, an array of periodically patterned indium-tin-oxide electrodes was first prepared on the LPI and bi-level structures were subsequently fabricated for the cell gap and the liquid crystal alignment. Our monolithic one-panel architecture allows the near-viewing distance property which is essential for mobile applications.

Dynamic Manipulation of Charged Lipids in Model Membrane for Bio-Microarrays.

We describe the dynamic manipulation of the charged lipids in a confined geometry where two dispersive factors arising from the random diffusion-based Brownian motion and the field-induced drift of target lipids compete with each other. It is found that the lateral distribution of the target lipids is well controlled through a combined effect of an external electric field and the geometric restrictions by the confinement. The dynamic manipulation scheme for the charged lipids in two-dimension would be useful for understanding the spatial organization of membrane components in a supported lipid membrane mimicking a real cell membrane and for producing membrane-based microarrays.

Continuity of Monolayer-Bilayer Junctions for Localization of Lipid Raft Microdomains in Model Membranes.

We show that the selective localization of cholesterol-rich domains and associated ganglioside receptors prefer to occur in the monolayer across continuous monolayer-bilayer junctions (MBJs) in supported lipid membranes. For the MBJs, glass substrates were patterned with poly(dimethylsiloxane) (PDMS) oligomers by thermally-assisted contact printing, leaving behind 3 nm-thick PDMS patterns. The hydrophobicity of the transferred PDMS patterns was precisely tuned by the stamping temperature. Lipid monolayers were formed on the PDMS patterned surface while lipid bilayers were on the bare glass surface. Due to the continuity of the lipid membranes over the MBJs, essentially free diffusion of lipids was allowed between the monolayer on the PDMS surface and the upper leaflet of the bilayer on the glass substrate. The preferential localization of sphingomyelin, ganglioside GM1 and cholesterol in the monolayer region enabled to develop raft microdomains through coarsening of nanorafts. Our methodology provides a simple and effective scheme of non-disruptive manipulation of the chemical landscape associated with lipid phase separations, which leads to more sophisticated applications in biosensors and as cell culture substrates.

Optically switchable grating based on dye-doped ferroelectric liquid crystal with high efficiency.

We demonstrate an all-optically switchable ferroelectric liquid crystal (FLC) grating constructed in an alternating binary configuration with different optical properties from domain to domain. A dye-doped FLC is uniformly aligned in one type of domains whereas it is infiltrated into the photo-polymerized networks of reactive mesogens in the other. Compared to conventional nematic LC cases, our FLC grating allows more efficient all-optical modulation and faster diffraction switching between the 0th and the 1st orders in subsecond since the optical response associated with the dye molecules in the layered state is less hindered than in the orientationally ordered state. Our dye-doped FLC grating with periodically infiltrated structures will be useful for designing a new class of all-optically switching systems.

Reconstituting ring-rafts in bud-mimicking topography of model membranes.

During vesicular trafficking and release of enveloped viruses, the budding and fission processes dynamically remodel the donor cell membrane in a protein- or a lipid-mediated manner. In all cases, in addition to the generation or relief of the curvature stress, the buds recruit specific lipids and proteins from the donor membrane through restricted diffusion for the development of a ring-type raft domain of closed topology. Here, by reconstituting the bud topography in a model membrane, we demonstrate the preferential localization of cholesterol- and sphingomyelin-enriched microdomains in the collar band of the bud-neck interfaced with the donor membrane. The geometrical approach to the recapitulation of the dynamic membrane reorganization, resulting from the local radii of curvatures from nanometre-to-micrometre scales, offers important clues for understanding the active roles of the bud topography in the sorting and migration machinery of key signalling proteins involved in membrane budding.

Biocompatible patterning of proteins on wettability gradient surface by thermo-transfer printing.

We develop a simple and biocompatible method of patterning proteins on a wettability gradient surface by thermo-transfer printing. The wettability gradient is produced on a poly(dimethylsiloxane) (PDMS)-modified glass substrate through the temperature gradient during thermo-transfer printing. The water contact angle on the PDMS-modified surface is found to gradually increase along the direction of the temperature gradient from a low to a high temperature region. Based on the wettability gradient, the gradual change in the adsorption and immobilization of proteins (cholera toxin B subunit) is achieved in a microfluidic cell with the PDMS-modified surface.