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Wen-Jong Ma

Publications and source records attributed to Wen-Jong Ma.

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Nematic and smectic liquid crystals modeling with stiff and free-joint Lennard-Jones chain molecules

Liquid crystals (LCs) composed of mesogens play important roles in various scientific and engineering problems. How a system with many mesogens can enter a LC state is an interesting and important problem. Using stiff and free-joint Lennard-Jones chain molecules as mesogens, we study the conditions under which the mesogens can enter various LC phases. The guideline is to eliminate the unwanted translational orders under a controlled fine-tuning procedure across a sequence of systems. Instead of monitoring the growth of order out of the disorder, we prepare a configuration of high orientation ordering and find out where it relaxes to. Such a procedure begins with a reference system, consisting of short chains of homogeneous soft spheres, in a liquid-vapor coexistence situation, at which the thermodynamic instability triggers a fast spontaneous growing process. By applying a short pulse of auxiliary field to align the dispersedly oriented clusters, followed by reducing the volume and, finally, changing the homogeneous molecules into heterogeneous chains, we are able to obtain a range of systems, including nematic and smectic LCs, at their stable ordered states. The model can be extended to study the influence of nanoparticles or external field on the LC structure.

cond-mat.soft

Can morphological changes of erythrocytes be driven by hemoglobin?

At 49 C erythrocytes undergo morphological changes due to an internal force, but the origin of the force that drives changes is not clear. Here we point out that our recent experiments on thermally induced force-release in hemoglobin can provide an explanation for the morphological changes of erythrocytes.

q-bio.BM

Universal geometrical factor of protein conformations as a consequence of energy minimization

The biological activity and functional specificity of proteins depend on their native three-dimensional structures determined by inter- and intra-molecular interactions. In this paper, we investigate the geometrical factor of protein conformation as a consequence of energy minimization in protein folding. Folding simulations of 10 polypeptides with chain length ranging from 183 to 548 residues manifest that the dimensionless ratio (V/(A )) of the van der Waals volume V to the surface area A and average atomic radius of the folded structures, calculated with atomic radii setting used in SMMP [Eisenmenger F., et. al., Comput. Phys. Commun., 138 (2001) 192], approach 0.49 quickly during the course of energy minimization. A large scale analysis of protein structures show that the ratio for real and well-designed proteins is universal and equal to 0.491\pm0.005. The fractional composition of hydrophobic and hydrophilic residues does not affect the ratio substantially. The ratio also holds for intrinsically disordered proteins, while it ceases to be universal for polypeptides with bad folding properties.

physics.bio-ph