Role Of Electrostatic Repulsion Research Articles

On the Role of Electrostatic Repulsion in Topological Defect-Driven Membrane Fission.

Within a modified Langevin Poisson–Boltzmann model of electric double layers, we derived an analytical expression for osmotic pressure between two charged surfaces. The orientational ordering of the water dipoles as well as the space dependencies of electric potentials, electric fields, and osmotic pressure between two charged spheres were taken into account in the model. Thus, we were able to capture the interaction between the parent cell and connected daughter vesicle or the interactions between neighbouring beads in necklace-like membrane protrusions. The predicted repulsion between them can facilitate the topological antidefect-driven fission of membrane daughter vesicles and the fission of beads of undulated membrane protrusions.

The Role of Electrostatic Repulsion on Increasing Surface Activity of Anionic Surfactants in the Presence of Hydrophilic Silica Nanoparticles

Hydrophilic silica nanoparticles alone are not surface active. They, however, develop a strong electrostatic interaction with ionic surfactants and consequently affect their surface behavior. We report the interfacial behavior of n-heptane/anionic-surfactant-solutions in the presence of hydrophilic silica nanoparticles. The surfactants are sodium dodecyl sulfate (SDS) and dodecyl benzene sulfonic acid (DBSA), and the diameters of the used particles are 9 and 30 nm. Using experimental tensiometry, we show that nanoparticles retain their non-surface-active nature in the presence of surfactants and the surface activity of surfactant directly increases with the concentration of nanoparticles. This fact was attributed to the electrostatic repulsive interaction between the negatively charged nanoparticles and the anionic surfactant molecules. The role of electrostatic repulsion on increasing surface activity of the surfactant has been discussed. Further investigations have been performed for screening the double layer charge of the nanoparticles in the presence of salt. Moreover, the hydrolysis of SDS molecules in the presence of silica nanoparticles and the interaction of nanoparticles with SDS inherent impurities have been studied. According to our experimental observations, silica nanoparticles alleviate the effects of dodecanol, formed by SDS hydrolysis, on the interfacial properties of SDS solution.

The role of electrostatic repulsion in the gelation of poly(vinyl alcohol)/borax aqueous solutions

This study examined linear viscoelasticity (LVE) of semidilute non-entangled poly(vinyl alcohol) (PVA) and borax aqueous solutions: one borax molecule dissociates into two B(OH)3 molecules and two B(OH)4- ions, and the latter can crosslink the PVA chains. Gelation was observed with increasing concentration of borax in the solutions. Analysis of LVE with the reversible gelation model reveals that although the number density of crosslinking ions increases with increasing concentration of borax, the fraction of the crosslinking ions decreases, which is attributed to the intensified electrostatic repulsion when more sites of the PVA chains are occupied by the ionic crosslinkers.

AuNPs‐Based Colorimetric Assay for Identification of Chicken Tissues in Meat and Meat Products

A simple colorimetric assay was developed to identify chicken tissues in meat and meat products by utilizing thiol‐labeled primers and unmodified gold nanoparticles (AuNPs). Primers were designed based on the chicken‐specific mitochondrial D‐loop gene. Polymerase chain reaction (PCR) is applied to amplify the target gene, and the PCR products labeled with thiol at one end were obtained. Following the mixing of AuNPs with the PCR products, the thiol binds to the surface of AuNPs, resulting in the formation of GNP‐PCR products. The resultant PCR products had abundant negative charges, which made AuNPs maintain dispersion under the role of electrostatic repulsion. As a result, in the presence of PCR products, AuNPs remained red in the presence of salt. In the absence of PCR products, the color of AuNPs changed from red to blue; therefore, the method described here could be exploited for the verification of chicken tissues with high accuracy.

Control of Collagen Stability and Heterotrimer Specificity through Repulsive Electrostatic Interactions.

Charge-pair interactions between acidic and basic residues on the surface of collagen can promote stability as well as control specificity of molecular recognition. Heterotrimeric collagen peptides have been engineered de novo using either rational or computational methods, which in both cases optimize networks of favorable charge-pair interactions in the target structure. Less understood is the role of electrostatic repulsion between groups of like charge in destabilizing structure or directing molecular recognition. To study this, we apply a “charge crowding” approach, where repulsive interactions between multiple aspartate side chains are found to destabilize the homotrimer states in triple helical peptide system and can be utilized to promote the formation of heterotrimers. Neutralizing surface charge by increasing salt concentration or decreasing pH can enhance homotrimer stability, confirming the role of charge crowding on the destabilization of homotrimers via electrostatic repulsion. Charge crowding may be used in conjunction with other approaches to create specific collagen heterotrimers.

Role of Electrostatic Repulsion in Controlling pH-Dependent Conformational Changes of Viral Fusion Proteins

Role of Electrostatic Repulsion in Controlling pH-Dependent Conformational Changes of Viral Fusion Proteins

Effects of the Electrostatic Repulsion Between Nanoparticles on Colorimetric Sensing: An Investigation of Determination of Hg2+ with Silver Nanoparticles

The electrostatic repulsion between metal nanoparticles has an important effect on the colorimetric assays based on the aggregation of nanoparticles. In this work, an Hg2+ colorimetric sensor based on silver nanoparticles (AgNPs) was used as a model system to study the effects of electrostatic repulsion. Adenine nucleotides carrying different numbers of phosphate groups, adenosine monophosphate (AMP), adenosine diphosphate, and adenosine triphosphate, were used to functionalize AgNPs, respectively. Three kinds of AgNPs displayed different responses to Hg2+ ions due to the difference in electrostatic repulsion force, which is resulted from the varying of the number of phosphate groups. The density of negative charges on the surface of AgNPs exhibited a great affect on the size of the AgNPs, detection sensitivity and response range for Hg2+ ions. On these bases, the AMP-modified AgNPs were developed into highly sensitive colorimetric sensor to determine Hg2+ ions in aqueous solution, which showed a high sensitivity of 0.5 nM and excellent selectivity for Hg2+. The Hg2+ levels in water samples were determined using AMP-AgNPs with satisfied recovery. The studies on the role of electrostatic repulsion in the colorimetric assays will facilitate the development of more sensitive colorimetric sensors.

Role of electrostatic repulsion on colloidal stability of Bacillus halmapalus alpha-amylase

The colloidal stability of charged particles in suspension is often controlled by electrostatic repulsion, which can be rationalized in a semi-quantitative way by the DLVO theory. In the current study, we investigate this approach towards understanding irreversible protein aggregation, using Bacillus halmapalus α-amylase (BHA) as a model protein. Repulsive forces between partly unfolded monomers were shown to strongly affect aggregation. Adding salt, increasing valence of counter ions or decreasing pH in the direction of p I resulted in a shift in the rate-limiting step from association to unfolding as evidenced by a change in aggregation kinetics from second to first-order in protein concentration. Charge screening effects by salts resulted in increased average size of protein aggregates but only moderately affected the secondary structure of protein within the aggregates. Salt and pH effects could be explained within the DLVO framework, indicating that partially unfolded BHA monomers can be modelled realistically as colloids with a random charge distribution.

Fluoroalcohols induced unfolding of Succinylated Con A: Native like β-structure in partially folded intermediate and α-helix in molten globule like state

Concanavalin A (Con A) exists in dimeric state at pH 5. In concentration range 20–60% (v/v) 2,2,2-trifluoroethanol (TFE) and 2–40% (v/v) 1,1,1,3,3,3-hexafluoroisopropanol (HFIP), Con A at pH 5.0 shows visible aggregation. However, when succinyl Con A was used, no aggregation was observed in the entire concentration range of fluoroalcohols (0–90% v/v TFE and HFIP) and resulted in stable α-helix formation. Temperature-induced concentration-dependent aggregation in Con A was also found to be prevented/reduced in succinylated form. Possible role of electrostatic repulsion among residues in the prevention of hydrophobically driven aggregation has been discussed. Results indicate that succinylation of a protein resulted in greater stability (in both β-sheet and α-helical forms) against alcohol-induced and temperature-induced concentration-dependent aggregation and this observation may play significant role in amyloid-forming proteins. Effect of TFE and HFIP on the conformation of a dimeric protein, Succinylated Con A, has been investigated by circular dichroism (CD), fluorescence emission spectroscopy, binding of hydrophobic dye ANS (8-anilinonaphthalene-1-sulfonic acid). Far UV-CD, a probe for secondary structure shows loss of native secondary structure in the presence of low concentration of both the alcohols, TFE (10% v/v) and HFIP (4% v/v). Upon addition of higher concentration of these alcohols, Succinylated Con A exhibited transformation from β-sheet to α-helical structure. Intrinsic tryptophan fluorescence studies, ANS binding and near UV-CD experiments indicate the protein is more expanded, have more exposed hydrophobic surfaces and highly disrupted tertiary structure at 60% (v/v) TFE and 30% (v/v) HFIP concentrations. Taken together, these results it might be concluded that TFE and HFIP induce two intermediate states at their low and high concentrations in Succinyl Con A.

Role of Electrostatic Repulsion on the Viscosity of Bidisperse Silica Suspensions

The flow behavior of bidisperse aqueous silica suspensions has been studied at different electrolyte concentrations as a function of shear rate, total volume fraction of the particles, and volume ratio of small to large particles. It is shown that the range of the electrostatic repulsion plays an important role in determining the viscosity of the suspension. Binary mixtures of particles of longer range repulsive forces showed higher viscosities than the suspensions of shorter range electrostatic interactions. Bimodal suspensions of long-range interactions showed non-Newtonian behavior over wider ranges of shear due to the deformation of the ionic cloud around the particles, which is larger in these systems. The viscosity of bimodal suspensions used in this study was scaled with respect to the viscosity of the related monosized systems and the viscosity of one bimodal suspension at a fixed total volume fraction of the particles, employing our earlier scaling method. The model normalizes the effect of colloidal forces by introducing a scaling factor that collapses the data into a single curve for bimodal suspensions of a particular size ratio, and it is shown that the model is valid for systems with both short-range and long-range repulsive forces.

Role of electrostatic repulsion in the acidic molten globule of cytochrome c

The molten globule has been assumed to be a major intermediate state of protein folding. To extend our understanding of protein folding it is important to elucidate the thermodynamic mechanism of conformational stability of the molten globule. To clarify the role of electrostatic charge repulsion in the stability of the acidic molten globule state, we prepared a series of acetylated horse ferricytochrome c species with various degrees of charge repulsion. On the basis of circular dichroism measurement, we show that the stability of the acidic molten globule is determined by a balance of electrostatic repulsions between positive residues, which favor the extended conformation, and the opposing forces, which stabilize the molten globule. These results provide a clear example of charge repulsions producing unfolding of the compact protein structure, and suggest that the reversibly denatured conformation of ferricytochrome c under physiological conditions (i.e. neutral pH, ambient temperature and no denaturant) is the molten globule.