The remarkable phenotypic variability of the p.Arg269HiS variant in the TRPV4 gene.

INTRODUCTION: Mutations in the TRPV4 gene are associated with neuromuscular disorders and skeletal dysplasias, which present a phenotypic overlap. METHODS: Next-generation sequencing and Sanger sequencing were used to analyze the TRPV4 gene. RESULTS: We present 2 Polish families with TRPV4-related disorder harboring the same p.Arg269His mutation. The disease phenotypic expression was extremely variable (from mild scapular winging to severe hypotonia, global weakness, inability to walk unaided, congenital contractures, scoliosis, and respiratory insufficiency), but did not suggest anticipation. The 2 most severely affected patients showed congenital distal contractures of the upper limbs and involvement of cranial nerves (manifesting as facial asymmetry and strabismus). The disease course seemed to be stable, although in later stages it caused respiratory insufficiency and progression of physical disability. DISCUSSION: The phenotypic variability observed in p.Arg269His carriers suggests that an additional modifier or a more complex pathogenic mechanism exists. Muscle Nerve 59:129-133, 2019.

Colloidal assembly directed by virtual magnetic moulds.

Interest in assemblies of colloidal particles has long been motivated by their applications in photonics, electronics, sensors and microlenses. Existing assembly schemes can position colloids of one type relatively flexibly into a range of desired structures, but it remains challenging to produce multicomponent lattices, clusters with precisely controlled symmetries and three-dimensional assemblies. A few schemes can efficiently produce complex colloidal structures, but they require system-specific procedures. Here we show that magnetic field microgradients established in a paramagnetic fluid can serve as 'virtual moulds' to act as templates for the assembly of large numbers (∼10(8)) of both non-magnetic and magnetic colloidal particles with micrometre precision and typical yields of 80 to 90 per cent. We illustrate the versatility of this approach by producing single-component and multicomponent colloidal arrays, complex three-dimensional structures and a variety of colloidal molecules from polymeric particles, silica particles and live bacteria and by showing that all of these structures can be made permanent. In addition, although our magnetic moulds currently resemble optical traps in that they are limited to the manipulation of micrometre-sized objects, they are massively parallel and can manipulate non-magnetic and magnetic objects simultaneously in two and three dimensions.

Treatment of the Lower Extremity Contracture/Deformities.

Lower extremity deformities of patients with arthrogryposis multiplex congenita present a wide spectrum of severity and deformity combinations. Treatment goals range from merely ensuring comfortable seating and shoe wear, to fully independent and active ambulation, but the overarching intention is to help realize the patient's greatest potential for independence and function. Treatment of hip and knee contractures and dislocations has become more interventional, whereas treatment of foot deformities has paradoxically become much less surgical. This article synopsizes the treatment strategies presented in September 2014 in Saint Petersburg, Russia at the second international symposium on arthrogryposis.

Engineering Gram Selectivity of Mixed-Charge Gold Nanoparticles by Tuning the Balance of Surface Charges.

Nanoparticles covered with ligand shells comprising both positively and negatively charged ligands exhibit Gram-selective antibacterial action controlled by a single experimental parameter, namely the proportion of [+] and [-] ligands tethered onto these particles. Gram selectivity is attributed to the interplay between polyvalent electrostatic and non-covalent interactions that work in unison to disrupt the bacterial cell wall. The [+/-] nanoparticles are effective in low doses, are non-toxic to mammalian cells, and are tolerated well in mice. These results constitute the first example of rational engineering of Gram selectivity at the (macro)molecular level.

Photoconductance and inverse photoconductance in films of functionalized metal nanoparticles.

In traditional photoconductors, the impinging light generates mobile charge carriers in the valence and/or conduction bands, causing the material's conductivity to increase. Such positive photoconductance is observed in both bulk and nanostructured photoconductors. Here we describe a class of nanoparticle-based materials whose conductivity can either increase or decrease on irradiation with visible light of wavelengths close to the particles' surface plasmon resonance. The remarkable feature of these plasmonic materials is that the sign of the conductivity change and the nature of the electron transport between the nanoparticles depend on the molecules comprising the self-assembled monolayers (SAMs) stabilizing the nanoparticles. For SAMs made of electrically neutral (polar and non-polar) molecules, conductivity increases on irradiation. If, however, the SAMs contain electrically charged (either negatively or positively) groups, conductivity decreases. The optical and electrical characteristics of these previously undescribed inverse photoconductors can be engineered flexibly by adjusting the material properties of the nanoparticles and of the coating SAMs. In particular, in films comprising mixtures of different nanoparticles or nanoparticles coated with mixed SAMs, the overall photoconductance is a weighted average of the changes induced by the individual components. These and other observations can be rationalized in terms of light-induced creation of mobile charge carriers whose transport through the charged SAMs is inhibited by carrier trapping in transient polaron-like states. The nanoparticle-based photoconductors we describe could have uses in chemical sensors and/or in conjunction with flexible substrates.

Label-free in situ optical monitoring of the adsorption of oppositely charged metal nanoparticles.

The mechanism of alternating deposition of oppositely charged gold nanoparticles (AuNPs) was investigated by optical waveguide lightmode spectroscopy (OWLS). OWLS allows monitoring of the kinetics of layer-by-layer (LbL) adsorption of positively and negatively charged nanoparticles in real time without using any labels so that the dynamics of layer formation can be revealed. Positively charged NPs that are already deposited on a negatively charged glass substrate strongly facilitate the adsorption of the negatively charged particles. The morphology of the adsorbed layer was also investigated with atomic force microscopy (AFM). AFM revealed that the interaction between oppositely charged particles results in the formation of NP clusters with sizes varying between 100 and 6000 NPs. The cluster size distribution is found to be an exponentially decaying function, and we propose a simple theory to explain this finding.

Biomechanical parameters of the BP-enriched bone cement.

Bisphosphonates (BPs) are well-known substances with very efficient antiresorptive properties. Their beneficial actions are useful not only in achieving better bone mineral density but also in improving bone microarchitecture, strength and, consequently, its quality. Surgical cement, being a polymer composite, is required to be highly biocompatible and biotolerant. The goal of the presented study was to assess whether the enrichment of cement with pamidronate has changed its biomechanical properties. We compared the biomechanical parameters of clean bone cement and BP-enriched bone cement, which were both used formerly in our rat models. Biomechanical properties of BP-enriched bone cement are defined by two basic terms: stress and strain, which are caused by the influence of external force. In the investigatory process of the bone's biomechanical parameters, the compressive test and the three-point flexural tests were used. During the three-point flexural investigation, the sample was supported at both ends and loaded in the middle, resulting in a flexure. After a specific range of flexure, the sample was fractured. In obtained results, there were no significant differences in the values of the stress determined at the point of maximal load and the energy stored in the samples for proportional stress-strain limit (elastic region). There were also no significant differences in the density of the samples. The study shows that the enrichment of bisphosphonates causes yielding of the bone cement material. In the presented data, we conclude that use of pamidronate implanted in bone cement did not have a detrimental effect on its biomechanical properties. Therefore, the obtained results encouraged us to perform further in vivo experiments which assess the biomechanical properties of bones implanted with BP-enriched bone cement.

Virtual Reality-Induced Modification of Vestibulo-Ocular Reflex Gain in Posturography Tests.

Background: The aim of the study was to demonstrate the influence of virtual reality (VR) exposure on postural stability and determine the mechanism of this influence. Methods: Twenty-six male participants aged 21-23 years were included, who underwent postural stability assessment twice before and after a few minute of single VR exposure. The VR projection was a computer-generated simulation of the surrounding scenery. Postural stability was assessed using the Sensory Organization Test (SOT), using Computerized Dynamic Posturography (CDP). Results: The findings indicated that VR exposure affects the visual and vestibular systems. Significant differences (p < 0.05) in results before and after VR exposure were observed in tests on an unstable surface. It was confirmed that VR exposure has a positive influence on postural stability, attributed to an increase in the sensory weight of the vestibular system. Partial evidence suggested that the reduction in vestibulo-ocular reflex (VOR) reinforcement may result in an adaptive shift to the optokinetic reflex (OKR). Conclusions: By modifying the process of environmental perception through artificial sensory simulation, the influence of VR on postural stability has been demonstrated. The validity of this type of research is determined by the effectiveness of VR techniques in the field of vestibular rehabilitation.

Controlled pH stability and adjustable cellular uptake of mixed-charge nanoparticles.

Nanoparticles functionalized with mixed self-assembled monolayers (m-SAMs) comprising positively and negatively charged thiols are stable at both low and high pH but precipitate sharply at the pH where the charges on the particle are balanced (pH(prec)). By adjusting the proportion of the positively and negatively charged ligands in the m-SAM or changing particle size, pH(prec) can be varied flexibly between ~4 and ~7. In addition, changes in the SAMs' composition and particles' net charge translate into different degrees of cellular uptake. Remarkably, the presence of the positively charged thiols allows for the uptake of particles having net negative charge.

Charged nanoparticles as supramolecular surfactants for controlling the growth and stability of microcrystals.

Microcrystals of desired sizes are important in a range of processes and materials, including controlled drug release, production of pharmaceutics and food, bio- and photocatalysis, thin-film solar cells and antibacterial fabrics. The growth of microcrystals can be controlled by a variety of agents, such as multivalent ions, charged small molecules, mixed cationic-anionic surfactants, polyelectrolytes and other polymers, micropatterned self-assembled monolayers, proteins and also biological organisms during biomineralization. However, the chief limitation of current approaches is that the growth-modifying agents are typically specific to the crystalizing material. Here, we show that oppositely charged nanoparticles can function as universal surfactants that control the growth and stability of microcrystals of monovalent or multivalent inorganic salts, and of charged organic molecules. We also show that the solubility of the microcrystals can be further tuned by varying the thickness of the nanoparticle surfactant layers and by reinforcing these layers with dithiol crosslinks.

How and why nanoparticle's curvature regulates the apparent pKa of the coating ligands.

Dissociation of ionizable ligands immobilized on nanopaticles (NPs) depends on and can be regulated by the curvature of these particles as well as the size and the concentration of counterions. The apparent acid dissociation constant (pK(a)) of the NP-immobilized ligands lies between that of free ligands and ligands self-assembled on a flat surface. This phenomenon is explicitly rationalized by a theoretical model that accounts fully for the molecular details (size, shape, conformation, and charge distribution) of both the NPs and the counterions.

Precision assembly of oppositely and like-charged nanoobjects mediated by charge-induced dipole interactions.

The range of electrostatic interactions controls precisely the mutual orientations of assembling charged nanoobjects. For nonspherically symmetric particles, polarization effects and induced dipoles can dominate charge-charge interactions. These charge-induced dipole interactions mediate orientation-specific aggregation of both oppositely and like-charged particles.

Liesegang rings engineered from charged nanoparticles.

Functionalized nanoparticles (NPs) serve as building blocks of self-organizing chemical patterns comprising periodic zones of nanoparticle precipitation. In contrast to ions, which underlie most pattern-forming chemical systems and whose properties cannot be readily modified, NPs allow for flexible adjustment of particle charges and/or material properties. In particular, changes in the particle charges control the precipitation behavior and ultimately the morphologies of the emerging patterns. The phenomenon of NP-based periodic precipitation is explained by reaction-diffusion modeling and can be used for the fractionation of NPs of different sizes.

Vesicle-to-micelle oscillations and spatial patterns.

A pH oscillator is coupled to and controls rhythmic interconversion of nanoscopic vesicles and micelles made of fatty acids. When changes in pH are combined with diffusion, self-assembly produces spatially extended patterns of vesicle/micelle "stripes" or concentric "shells".

Size selection during crystallization of oppositely charged nanoparticles.

Opposites attract (selectively): Oppositely charged nanoparticles characterized by different size distributions form 3D supracrystals (see figure) only if the distributions overlap. Crystal quality decreases rapidly with decreasing degree of overlap, and, irrespective of the ratio of particle diameters/charges, no crystals are observed for non-overlapping distributions.

Rapid deposition of hydrophobic nanoparticle monolayers onto hydrophilic surfaces from liquid-liquid interfaces.

Dense, hydrophobic coatings comprising hydrophilic nanoparticles are deposited rapidly from water/toluene emulsions. The process of deposition is driven by a subtle interplay between interfacial phenomena, electrostatic interparticle repulsions, and hydrogen bonding between the NPs and the substrate(s). The packing fractions and the plasmonic properties of the coatings can be controlled by the pH of the aqueous phase. Once formed, the coatings can be further functionalized without a loss of mechanical integrity.

Precipitation of oppositely charged nanoparticles by dilution and/or temperature increase.

Mixtures of oppositely charged nanoparticles (NPs) exhibit anomalous solubility behavior and precipitate either upon dilution or upon temperature increase. Precipitation is reversible and can be explained by a thermodynamic model that accounts for changes in the electrostatic interactions due to the adsorption/desorption of counterions from the surface of the NPs. Specifically, decreasing the salt concentration via dilution or increasing the temperature causes dissociation of counterions from the NP surfaces, increasing the magnitude of electrostatic interactions between NPs and resulting in their precipitation. Model predictions of NP solubility are in quantitative agreement with the experimental observations. Such predictions are of practical importance for the preparation of "patchy" electrostatic coatings and ionic-like NP supracrystals.

Mechanism of the cooperative adsorption of oppositely charged nanoparticles.

Quartz crystal microbalance experiments were performed to study the kinetics of surface adsorption from solutions containing oppositely charged nanoparticles. A theoretical model was developed according to which formation of dense nanoparticle (NP) monolayers is driven by a cooperative process, in which the already-adsorbed NPs facilitate adsorption of NPs from solution. The kinetic rate constants change with the NP solution concentration and can be used to backtrack adsorption free energies. These energies agree with the predictions of a simple DLVO model.

Correction: Electrostatics at the nanoscale.

Correction for 'Electrostatics at the nanoscale' by David A. Walker et al., Nanoscale, 2011, 3, 1316-1344.

Electrostatically "patchy" coatings via cooperative adsorption of charged nanoparticles.

Solutions containing oppositely charged nanoparticles (NPs) deposit "patchy" coatings of alternating charge distribution on various types of materials, including polymers, elastomers, and semiconductors. Surface adsorption of the NPs is driven by cooperative electrostatic interactions and does not require chemical ligation or layer-by-layer schemes. The composition and the quality of the coatings can be regulated by the types, the charges, and the relative concentrations of the NPs used and by the pH. Dense coatings form on flat, curvilinear, or micropatterned surfaces, are stable against common chemicals for prolonged periods of time, and can be used in applications ranging from bacterial protection to plasmonics.