Equilibrium Bundle Size of Rodlike Polyelectrolytes with Counterion-Induced Attractive Interactions

Multivalent counterions can induce an effective attraction between like-charged rodlike polyelectrolytes, leading to the formation of polelectrolyte bundles. In this paper, we calculate the equilibrium bundle size using a simple model in which the attraction between polyelectrolytes (assumed to be pairwise additive) is treated phenomenologically. If the counterions are point-like, they almost completely neutralize the charge of the bundle, and the equilibrium bundle size diverges. When the counterions are large, however, steric and short-range electrostatic interactions prevent charge neutralization of the bundle, thus forcing the equilibrium bundle size to be finite. We also consider the possibility that increasing the number of nearest neighbors for each rod in the bundle frustrates the attractive interaction between the rods. Such a frustration leads to the formation of finite size bundles as well, even when the counterions are small.Comment: 4 pages, 2 figures; v2: typos corrected, references added, minor changes made to conten

Binding of Oppositely Charged Membranes and Membrane Reorganization

We consider the electrostatic interaction between two rigid membranes, with different surface charge densities of opposite sign, across an aqueous solution without added salt. Exact solutions to the nonlinear Poisson-Boltzmann equation are obtained and their physical meaning discussed. We also calculate the electrostatic contribution to the free energy and discuss the renormalization of the area per head group of the charged lipids arising from the Coulomb interaction.Comment: 13 pages, 6 figures, to be published in EJP

Polyelectrolyte-colloid complexes: polarizability and effective interaction

We theoretically study the polarizability and the interactions of neutral complexes consisting of a semi-flexible polyelectrolyte adsorbed onto an oppositely charged spherical colloid. In the systems we studied, the bending energy of the chain is small compared to the Coulomb energy and the chains are always adsorbed on the colloid. We observe that the polarizability is large for short chains and small electrical fields and shows a non-monotonic behavior with the chain length at fixed charge density. The polarizability has a maximum for a chain length equal to half of the circumference of the colloid. For long chains we recover the polarizability of a classical conducting sphere. For short chains, the existence of a permanent dipole moment of the complexes leads to a van der Waal's-type long-range attraction between them. This attractive interaction vanishes for long chains (i.e., larger than the colloidal size), where the permanent dipole moment is negligible. For short distances the complexes interact with a deep short-ranged attraction which is due to energetic bridging for short chains and entropic bridging for long chains. Exceeding a critical chain length eventually leads to a pure repulsion. This shows that the stabilization of colloidal suspensions by polyelectrolyte adsorption is strongly dependent on the chain size relative to the colloidal size: for long chains the suspensions are always stable (only repulsive forces between the particles), while for mid-sized and short chains there is attraction between the complexes and a salting-out can occur.Comment: 13 pages, 14 figure

Interactions Between Charged Rods Near Salty Surfaces

Using both theoretical modeling and computer simulations we study a model system for DNA interactions in the vicinity of charged membranes. We focus on the polarization of the mobile charges in the membranes due to the nearby charged rods (DNA) and the resulting screening of their fields and inter-rod interactions. We find, both within a Debye-Huckel model and in Brownian dynamics simulations, that the confinement of the mobile charges to the surface leads to a qualitative reduction in their ability to screen the charged rods to the degree that the fields and resulting interactions are not finite-ranged as in systems including a bulk salt concentration, but rather decay algebraically and the screening effect is more like an effective increase in the multipole moment of the charged rod

Long-Range Interaction between Heterogeneously Charged Membranes

Despite their neutrality, surfaces or membranes with equal amounts of positive and negative charge can exhibit long-range electrostatic interactions if the surface charge is heterogeneous; this can happen when the surface charges form finite-size domain structures. These domains can be formed in lipid membranes where the balance of the different ranges of strong but short-ranged hydrophobic interactions and longer-ranged electrostatic repulsion result in a finite, stable domain size. If the domain size is large enough, oppositely charged domains in two opposing surfaces or membranes can be strongly correlated by the elecrostatic interactions; these correlations give rise to an attractive interaction of the two membranes or surfaces over separations on the order of the domain size. We use numerical simulations to demonstrate the existence of strong attractions at separations of tens of nanometers. Large line tensions result in larger domains but also increase the charge density within the domain. This promotes correlations and, as a result, increases the intermembrane attraction. On the other hand, increasing the salt concentration increases both the domain size and degree of domain anticorrelation, but the interactions are ultimately reduced due to increased screening. The result is a decrease in the net attraction as salt concentration is increased

A lattice model of hydrophobic interactions

Hydrogen bonding is modeled in terms of virtual exchange of protons between water molecules. A simple lattice model is analyzed, using ideas and techniques from the theory of correlated electrons in metals. Reasonable parameters reproduce observed magnitudes and temperature dependence of the hydrophobic interaction between substitutional impurities and water within this lattice.Comment: 7 pages, 3 figures. To appear in Europhysics Letter

David Grove\u27s Metaphors for Healing

Within the ever-expanding list of approaches to psychotherapy, there is a tendency to overlook deep imagery approaches. The current article reports on one such metaphor-based therapy developed by David Grove (Grove & Panzer, 1989). The approach is analyzed within the context of mainstream contemporary psychotherapy in general, the state of empirical understanding of common processes to psychotherapy, and in relation to other deep imagery-based approaches to therapy. Next, a step-by-step description of the techniques used within metaphor therapy are presented, along with a case example demonstrating the use of these techniques on a case involving pain symptoms. Finally, it is argued that deep imagery approaches in general, and Grove’s approach in particular, may provide a means for greater theoretical integration within integrative healthcare

Counterion density profiles at charged flexible membranes

Counterion distributions at charged soft membranes are studied using perturbative analytical and simulation methods in both weak coupling (mean-field or Poisson-Boltzmann) and strong coupling limits. The softer the membrane, the more smeared out the counterion density profile becomes and counterions pentrate through the mean-membrane surface location, in agreement with anomalous scattering results. Membrane-charge repulsion leads to a short-scale roughening of the membrane.Comment: 4 pages, 4 figure