arXiv subjects

Yu-qiang Ma

Publications and source records attributed to Yu-qiang Ma.

24 records · Page 2Linked to original sources

arXiv2007

Structure and organization in inclusion-containing bilayer membranes

Membrane organization is essential for cellular functions such as signal transduction and membrane trafficking. A major challenge is to understand the lateral heterogeneous structures in membranes and membrane fluidity in the presence of inclusions. Based on a considerable amount of experimental evidence for lateral organization of lipid membranes which share astonishingly similar features in the presence of different inclusions, we first present a general model system of bilayer membranes embedded by nanosized inclusions, and explain experimental findings. Here, the hydrophobic inclusions are simple models of intrinsic membrane proteins, cholesterol embedded in the membrane, hydrophobic drugs, or other nanoparticles for bio-medical applications. It is found that lipid/inclusion-rich raft domains are formed at moderate inclusion concentrations, and disappear with the increase of inclusions. At high inclusion content, chaining of inclusions occurs due to the effective attraction between inclusions mediated by lipids. Meanwhile, increasing inclusions can also cause thickening of the membrane, and the distribution of inclusions undergoes a layering transition from one-layer located in the bilayer midplane to two-layer structure arranged into the two leaflets of a bilayer. Our theoretical predictions address the complex interactions between membranes and inclusions, suggesting a unifying mechanism which reflects the competition between the conformational entropy of lipids favoring the formation of lipid-rich rafts and the steric repulsion of inclusions leading to the uniform dispersion.

cond-mat.soft↗

arXiv2006

Layer-by-layer assembly of colloidal particles deposited onto the polymer-grafted elastic substrate

We demonstrate a novel route of spatially organizing the colloid arrangements on the polymer-grafted substrate by use of self-consistent field and density functional theories. We find that grafting of polymers onto a substrate can effectively control spatial dispersions of deposited colloids as a result of the balance between colloidal settling force and entropically elastic force of brushes, and colloids can form unexpected ordered structures on a grafting substrate. The depositing process of colloidal particles onto the elastic "soft" substrate includes two steps: brush-mediated one-dimensional arrangement of colloidal crystals and controlled layer-by-layer growth driven entropically by non-adsorbing polymer solvent with increasing the particles. The result indicates a possibility for the production of highly ordered and defect-free structures by simply using the grafted substrate instead of periodically patterned templates, under appropriate selection of colloidal size, effective depositing potential, and brush coverage density.

cond-mat.soft↗

arXiv2006

Effective Attraction Interactions between Like-charge Macroions Bound to Binary Fluid Lipid Membranes

Using integral equation theory of liquids to a binary mixed fluid lipid membrane, we study the membrane-mediated interactions between the macroions and the redistribution of neutral and charged lipids due to binding macroions. We find that when the concentration of binding macroions is infinitely dilute, the main contribution to the attractive potential between macroions is the line tension between neutral and charged lipids of the membrane, and the bridging effect also contributes to the attraction. As the relative concentration of charged lipids is increased, we observe a repulsive - attractive - repulsive potential transition due to the competition between the line tension of lipids and screened electrostatic macroion-macroion interactions. For the finite concentration of macroions, the main feature of the attraction is similar to the infinite dilution case. However, due to the interplay of formation of charged lipid - macroion complexes, the line tension of redistributed binary lipids induced by single macroion is lowered in this case, and the maximum of attractive potential will shift toward the higher values of the charged lipid concentration.

cond-mat.soft↗

arXiv2006

Lateral organization in mixed lipid bilayers supported on a geometrically patterned substrate

The organization of lipids in biological membranes is essential for cellular functions such as signal transduction and membrane trafficking. A major challenge is how to control lateral lipid composition in supported membranes which are crucial for the design of biosensors and investigation of cellular processes. Here, we undertake the first theoretical study of lateral organization of mixed lipids in bilayers induced by a geometrically patterned substrate, and examine the physical mechanism of patterned substrate-induced structural formation in the supported lipid bilayers. A rich variety of composition segregations of lipids are regulated, and the results can account well for most recent experimental works [Yoon, T. Y. et al. \textit{Nat. Mater.} \textbf{5}, 281(2006) and Parthasarathy, R. et al. \textit{Langmuir} \textbf{22}, 5095(2006)]. The present study provides a comprehensive understanding of mechanically controlling the spatial organization of membrane components by unifying these experimental evidences.

cond-mat.soft↗

arXiv2006

Phase Behavior in Thin Films of Confined Colloid-Polymer Mixtures

Using self-consistent field and density-functional theories, we first investigate colloidal self-assembling of colloid/polymer films confined between two soft surfaces grafted by polymers. With the increase of colloidal concentrations, the film undergoes a series of transitions from disordered liquid $\to$ sparse square $\to$ hexagonal (or mixed square-hexagonal) $\to$ dense square $\to$ cylindric structures in plane, which results from the competition between the entropic elasticity of polymer brushes and the steric packing effect of colloidal particles. A phase diagram displays the stable regions of different in-layer ordering structures as the colloidal concentration is varied and layering transitions as the polymer-grafted density is decreased. Our results show a new control mechanism to stabilize the ordering of structures within the films.

cond-mat.soft↗

arXiv2006

Interactions between colloidal particles induced by polymer brushes grafted onto the substrate

We investigate the interaction energy between two colloidal particles on or immersed in nonadsorbing polymer brushes grafted onto the substrate as a function of the separation of the particles by use of self-consistent field theory calculation. Depending on the colloidal size and the penetration depth, we demonstrate an existence of repulsive energy barrier of several $k_{B}T$, which can be interpreted by separating the interaction energy into three parts: colloids-polymer interfacial energy, entropic contribution due to ``depletion zone" overlap of colloidal particles, and entropically elastic energy of grafted chains by compression of particles. The existence of repulsive barrier which is of entirely entropic origin, can lead to kinetic stabilization of the mixture rather than depletion flocculation or phase separation. Therefore, the present result may suggest an approach to control the self-assembling behavior of colloids for the formation of target structures, by tuning the colloidal interaction on the grafting substrate under appropriate selection of colloidal size, effective gravity (influencing the penetration depth), and brush coverage density.

cond-mat.soft↗