Impact of transmembrane peptides on individual lipid motions and collective dynamics of lipid bilayers.

The fluid nature of lipid bilayers is indispensable for the dynamic regulation of protein function and membrane morphology in biological membranes. Membrane-spanning domains of proteins interact with surrounding lipids and alter the physical properties of lipid bilayers. However, there is no comprehensive view of the effects of transmembrane proteins on the membrane's physical properties. Here, we investigated the effects of transmembrane peptides with different flip-flop-promoting abilities on the dynamics of a lipid bilayer employing complemental fluorescence and neutron scattering techniques. The quasi-elastic neutron scattering and fluorescence experiments revealed that lateral diffusion of the lipid molecules and the acyl chain motions were inhibited by the inclusion of transmembrane peptides. The neutron spin-echo spectroscopy measurements indicated that the lipid bilayer became more rigid but more compressible and the membrane viscosity increased when the transmembrane peptides were incorporated into the membrane. These results suggest that the inclusion of rigid transmembrane structures hinders individual and collective lipid motions by slowing down lipid diffusion and increasing interleaflet coupling. The present study provides a clue for understanding how the local interactions between lipids and proteins change the collective dynamics of the lipid bilayers, and therefore, the function of biological membranes.

Topologically Protected Generation of Stable Wall Loops in Nematic Liquid Crystals.

The nematic liquid crystal (LC) director field can contain defects that are both singular and nonsingular, but nonsingular defects with an integer winding number of the director are typically metastable because of their high energy. We demonstrate topology-mediated generation and stabilization of nonsingular wall loops in a sandwich-type LC cell by combining a patterned substrate with a planar substrate. We implement a design which imposes a topological constraint on a singular disclination loop such that it irreversibly annihilates upon application of a field, and it results in the generation of a stable nonsingular wall loop when the field is removed. Theoretical modeling agrees with experimental observations, providing insight into the wall generation mechanism and its stability. The concept to stabilize high-energy structures through orientation-patterning-defined topological constraints extends our ability to control orientationally ordered matter.

Shape control of surface-stabilized disclination loops in nematic liquid crystals.

Recent studies on topological defects in conventional and active nematic liquid crystals have revealed their potential as sources of advanced functionality whereby the collective behavior of the constituent molecules or cells is controlled. On the other hand, the fact that they have high energies and are metastable makes their shape control a nontrivial issue. Here, we demonstrate stabilization of arbitrary-shaped closed disclination loops with 1/2 strength floating in the bulk by designing the twist angle distribution in a liquid crystal cell. Continuous variation of the twist angle from below to above |π/2| allows us to unambiguously position reverse twist disclinations at will. We also analyze the elastic free energy and uncover the relationship between the twist angle pattern and shrink rate of the surface-stabilized disclination loop.

Field strength and frequency tunable, two-way rotation of liquid crystal micro-particles dispersed in a liquid crystal host.

Liquid crystal (LC) micro-particles are functional materials possessing anisotropies of LCs originating from their inner molecular alignment, and are fabricated by polymerizing pre-aligned rod-like molecules in the LC state. Here we demonstrate field strength and frequency tunable two-way rotation control of LC micro-particles in a LC host, and unravel its mechanism by theoretically calculating the contributing free energies. Cuboid-shaped micro-particles with inner molecular alignment along the long axis are fabricated via two-photon excited direct laser writing, and dispersed in a dual-frequency (DF) LC to be electrically driven by a voltage applied in the in-plane direction of the cell. Under an electric field, the particles rotate either clockwise or anticlockwise to align the inner molecular alignment parallel or perpendicular to the applied field; however, unlike conventional LCs, the rotation direction depends not only on the frequency, but also on the strength of the field. The complex motion is found to be the result of a delicate balance between the elastic energy of the host LC around the particle and the electrostatic energies of the host and the particle. Understanding complex rotational motion in LC/LC-particle composites is a step towards the development of advanced switching materials with superior performance.

Reversible switching of liquid crystal micro-particles in a nematic liquid crystal.

Liquid crystal micro-particles are functional materials possessing optical and dielectric anisotropies originating from the arrangement of rod-like molecules within the particles. Although they can be switched by an electric field, particles dispersed in isotropic hosts usually cannot return to their original state, because there is no restoration force acting on the particles. Here, we describe reversible switching of liquid crystal micro-particles by dispersing them in a nematic liquid crystal host. We fabricate square micro-particles with unidirectional molecular alignment and investigate their static and dynamic electro-optic properties by applying an in-plane electric field. The behavior of the micro-particles is well-described by the theoretical model we construct, making this study potentially useful for the development of liquid crystal-liquid crystal particle composites with engineered properties.