Efficient Nucleation Research Articles

The XMAP215 Ortholog Alp14 Promotes Microtubule Nucleation in Fission Yeast

The organization and number of microtubules (MTs) in a cell depend on the proper regulation of MT nucleation. Currently, the mechanism of nucleation is the most poorly understood aspect of MT dynamics. XMAP215/chTOG/Alp14/Stu2 proteins are MT polymerases that stimulate MT polymerization at MT plus ends by binding and releasing tubulin dimers. Although these proteins also localize to MT organizing centers and have nucleating activity invitro, it is not yet clear whether these proteins participate in MT nucleation invivo. Here, we demonstrate that in the fission yeast Schizosaccharomyces pombe, the XMAP215 ortholog Alp14 is critical for efficient MT nucleation invivo. In multiple assays, loss of Alp14 function led to reduced nucleation rate and numbers of interphase MT bundles. Conversely, activation of Alp14 led to increased nucleation frequency. Alp14 associated with Mto1 and γ-tubulin complex components, and artificially targeting Alp14 to the γ-tubulin ring complexes (γ-TuRCs) stimulated nucleation. In imaging individual nucleation events, we found that Alp14 transiently associated with a γ-tubulin particle shortly before the appearance of a new MT. The transforming acidic coiled-coil (TACC) ortholog Alp7 mediated the localization of Alp14 at nucleation sites but notplus ends, and was required for efficient nucleation but not for MT polymerization. Our findings provide the strongest evidence to date that Alp14 serves as a critical MT nucleation factor invivo. We suggest a model in which Alp14 associates with the γ-tubulin complex in an Alp7-dependent manner to facilitate the assembly or stabilization of the nascent MT.

XMAP215 is a microtubule nucleation factor that functions synergistically with the γ-tubulin ring complex.

How microtubules (MT) are generated in the cell is a major question in understanding how the cytoskeleton is assembled. For several decades, γ-tubulin has been accepted as the cell’s universal MT nucleator. Although there is evidence that γ-tubulin complexes are not the sole MT nucleators, identification of other nucleation factors has proven difficult. Here, we report that the well-characterized MT polymerase XMAP215 (chTOG/Msps/Stu2p/Alp14/Dis1 homologue) is essential for MT nucleation in Xenopus egg extracts. The concentration of XMAP215 determines the extent of MT nucleation. Even though XMAP215 and γ-tubulin ring complex (γ-TuRC) possess minimal nucleation activity individually, together these factors synergistically stimulate MT nucleation in vitro. The N-terminal TOG domains 1–5 of XMAP215 bind αβ-tubulin and promote MT polymerization, while the conserved C-terminus is required for efficient MT nucleation and directly binds γ-tubulin. In sum, XMAP215 and γ-TuRC together function as the principal nucleation module that generates MTs in cells.

XMAP215 joins microtubule nucleation team.

De novo assembly of microtubules, nucleation, has remained surprisingly enigmatic, considering that microtubules are polymers of only two proteins, α- and β-tubulin, and that γ-tubulin has a well-established role as nucleator. Now, the tubulin polymerase XMAP215 is shown to be required for efficient nucleation in cooperation with γ-tubulin.

Skyrmions in Magnetic Tunnel Junctions.

In this work, we demonstrate that skyrmions can be nucleated in the free layer of a magnetic tunnel junction (MTJ) with Dzyaloshinskii-Moriya interactions (DMIs) by a spin-polarized current with the assistance of stray fields from the pinned layer. The size, stability, and number of created skyrmions can be tuned by either the DMI strength or the stray field distribution. The interaction between the stray field and the DMI effective field is discussed. A device with multilevel tunneling magnetoresistance is proposed, which could pave the ways for skyrmion-MTJ-based multibit storage and artificial neural network computation. Our results may facilitate the efficient nucleation and electrical detection of skyrmions.

The synergistic role of azeotropic solvent mixtures and atactic polystyrene on the morphology, crystallization and field effect mobility of thin film 6,13-bis(triisopropylsilylethynyl)-pentacene based semiconductors

The effect of anisole/decane binary solvent mixture and the subsequent addition of low wt% aPS on 6,13-bis(triisopropylsilylethynyl)-pentacene (TIPS-pentacene) thin film morphology is investigated by optical microscopy, AFM and UV–Vis measurements. We show that, over the composition range anisole/decane of 96/4 to 85/15 wt%, the solution maintains an azeotropic composition with the boiling point of the binary mixture remaining constant at 152 °C, and the solvent composition remaining constant during evaporation and drying. It was found that addition of up to 20 wt% decane has little impact on micro-scale crystal morphology but has a significant influence on the growth mode and terrace roughness. The formation of large crystals is explained in terms of the change in solvent, increase in decane content, weakening the solute–solvent interactions and promoting efficient nucleation of the favoured H-aggregates of TIPS-pentacene. The effect of the TIPS-pentacene—aPS ratio up to 20 wt% for drop-cast thin film was similarly investigated. It is found that addition of aPS has a significant effect on both macroscopic crystal properties such as surface coverage, unity of orientation and long range order. It also changes the surface morphology and layer ordering on the nano-scale.

Purely Inorganic Highly Efficient Ice Nucleating Particle.

To evaluate the role of atmospheric heterogeneous reactions on the ice nucleation ability of airborne dust particles, we investigated the systematic study of ice nucleation microphysics with a suite of atmospherically relevant metals (10), halides (4), and oxyhalides (2). Within a minute, a kaolin–iron oxide composite (KaFe) showed efficient reactions with aqueous mercury salts. Among the different mercury salts tested, only HgCl2 reacting with KaFe generated HgKaFe, a highly efficient ice nucleating particle (HEIN). When added to water, HgKaFe caused water to freeze at much warmer temperatures, within a narrow range of −6.6 to −4.7 °C. Using a suite of optical spectroscopy, mass spectrometry, and microscopy techniques, we performed various experiments to decipher the physical and chemical properties of surface and bulk. KaFe was identified as a mixture of different iron oxides, namely, goethite, hematite, magnetite, and ε-Fe2O3, with kaolin. In HgKaFe, HgCl2 was reduced to Hg2Cl2 and iron was predominantly in maghemite form. Reduction of Fe2+ by NaBH4, followed by aerial oxidation, helped KaFe to be an exact precursor for the synthesis of HEIN HgKaFe. Kaolin served as a template for synthesizing iron oxide, opposing unwanted aggregation. No other metal or metal halide was found to have more efficient nucleating particles than HgCl2 with KaFe composite. The chelation of Hg(II) hindered the formation of HEIN. This study is useful for investigating the role of morphology and how inorganic chemical reactions on the surface of dust change morphology and thus ice nucleation activity. The understanding of the fundamentals of what makes a particle to be a good ice nucleating particle is valuable to further understand and predict the amount and types of atmospheric ice nucleating particles.

Nonthermal ice nucleation observed at distorted contact lines of supercooled water drops.

Ice nucleation is the crucial step for ice formation in atmospheric clouds and therefore underlies climatologically relevant precipitation and radiative properties. Progress has been made in understanding the roles of temperature, supersaturation, and material properties, but an explanation for the efficient ice nucleation occurring when a particle contacts a supercooled water drop has been elusive for over half a century. Here, we explore ice nucleation initiated at constant temperature and observe that mechanical agitation induces freezing of supercooled water drops at distorted contact lines. Results show that symmetric motion of supercooled water on a vertically oscillating substrate does not freeze, no matter how we agitate it. However, when the moving contact line is distorted with the help of trace amounts of oil or inhomogeneous pinning on the substrate, freezing can occur at temperatures much higher than in a static droplet, equivalent to ∼10^{10} increase in nucleation rate. Several possible mechanisms are proposed to explain the observations. One plausible explanation among them, decreased pressure due to interface curvature, is explored theoretically and compared with the observational results quasiquantitatively. Indeed,theobserved freezing-temperature increase scales with contact line speed in a manner consistent with the pressure hypothesis. Whatever the mechanism, the experiments demonstrate a strong preference for ice nucleation at three-phase contact lines compared to the two-phase interface, and they also show that movement and distortion of the contact line are necessary contributions to stimulating the nucleation process.

What makes a good descriptor for heterogeneous ice nucleation on OH-patterned surfaces

Freezing of water is arguably one of the most common phase transitions on Earth and almost always happens heterogeneously. Despite its importance, we lack a fundamental understanding of what makes substrates efficient ice nucleators. Here we address this by computing the ice nucleation (IN) ability of numerous model hydroxylated substrates with diverse surface hydroxyl (OH) group arrangements. Overall, for the substrates considered, we find that neither the symmetry of the OH patterns nor the similarity between a substrate and ice correlate well with the IN ability. Instead, we find that the OH density and the substrate-water interaction strength are useful descriptors of a material's IN ability. This insight allows the rationalization of ice nucleation ability across a wide range of materials, and can aid the search and design of novel potent ice nucleators in the future.

Efficient and controlled domain wall nucleation for magnetic shift registers

Ultrathin ferromagnetic strips with high perpendicular anisotropy have been proposed for the development of memory devices where the information is coded in tiny domains separated by domain walls. The design of practical devices requires creating, manipulating and detecting domain walls in ferromagnetic strips. Recent observations have shown highly efficient current-driven domain wall dynamics in multilayers lacking structural symmetry, where the walls adopt a chiral structure and can be driven at high velocities. However, putting such a device into practice requires the continuous and synchronous injection of domain walls as the first step. Here, we propose and demonstrate an efficient and simple scheme for nucleating domain walls using the symmetry of the spin orbit torques. Trains of short sub-nanosecond current pulses are injected in a double bit line to generate a localized longitudinal Oersted field in the ferromagnetic strip. Simultaneously, other current pulses are injected through the heavy metal under the ferromagnetic strip. Notably, the Slonczewski-like spin orbit torque assisted by the Oersted field allows the controlled injection of a series of domain walls, giving rise to a controlled manner for writing binary information and, consequently, to the design of a simple and efficient domain wall shift register.

Simultaneous measurements of new particle formation at 1 s time resolution at a street site and a rooftop site

Abstract. This study is the first to use two identical Fast Mobility Particle Sizers for simultaneous measurement of particle number size distributions (PNSDs) at a street site and a rooftop site within 500 m distance in wintertime and springtime to investigate new particle formation (NPF) in Beijing. The collected datasets at 1 s time resolution allow deduction of the freshly emitted traffic particle signal from the measurements at the street site and thereby enable the evaluation of the effects on NPF in an urban atmosphere through a site-by-site comparison. The number concentrations of 8 to 20 nm newly formed particles and the apparent formation rate (FR) in the springtime were smaller at the street site than at the rooftop site. In contrast, NPF was enhanced in the wintertime at the street site with FR increased by a factor of 3 to 5, characterized by a shorter NPF time and higher new particle yields than at the rooftop site. Our results imply that the street canyon likely exerts distinct effects on NPF under warm or cold ambient temperature conditions because of on-road vehicle emissions, i.e., stronger condensation sinks that may be responsible for the reduced NPF in the springtime but efficient nucleation and partitioning of gaseous species that contribute to the enhanced NPF in the wintertime. The occurrence or absence of apparent growth for new particles with mobility diameters larger than 10 nm was also analyzed. The oxidization of biogenic organics in the presence of strong photochemical reactions is suggested to play an important role in growing new particles with diameters larger than 10 nm, but sulfuric acid is unlikely to be the main species for the apparent growth. However, the number of datasets used in this study is relatively small, and larger datasets are essential to draw a general conclusion.

Frontispiece: Solvent Geometry Regulated Cooperative Supramolecular Polymerization

In the present examples of self-assembly of a naphthalene–diimide building block, linear hydrocarbon solvents directly participate in the nucleation step owing to a geometry allowed, favorable mixing with peripheral alkyl chains of the monomer, which leads to a cooperative supramolecular polymerization pathway. In sharp contrast, lack of such efficient nucleation leads to ill-defined polymerization pathway in cyclic hydrocarbons. However, in the presence of a small amount of additive (preformed fiber in linear alkanes), cooperative polymerization pathway could be retrieved even in cyclic alkanes. For more information, see the Full Paper by S. Ghosh et al. on page 10536 ff.

Preparation and thermal properties of Glauber’s salt-based phase-change materials for Qinghai–Tibet Plateau solar greenhouses

This paper reports the preparation and characterization of eutectic Glauber’s salt-based composite, phase-change materials (G-PCMs). PCMs were prepared using industrial-grade sodium sulfate decahydrate (Na2SO4 ⋅ 10H2O) as the basic material. Other salts were added to obtain the eutectic Glauber’s salt-based PCMs with phase-change temperatures of 25[Formula: see text]C, 15[Formula: see text]C and 10[Formula: see text]C. The modification of the G-PCMs was designed using the same experimental method to select the efficient nucleating, thickening and thermal conductive agents. The results show that borax can be an effective nucleating agent, sodium carboxymethyl cellulose is an excellent thickener and carbon powder is a good thermal conductive agent. The phase-change temperature, latent heat and thermal conductivity of the three different PCMs are 23.9[Formula: see text]C, 15.4[Formula: see text]C and 9.5[Formula: see text]C; 179.6, 129 and 116.2 J/g; and 1.02, 1.10 and 1.23 W/(m K), respectively. These PCMs possess suitable phase-change temperature, high latent heat and good thermal conductivity, and can be used in Qinghai–Tibet Plateau agricultural solar greenhouses.

Influence of Mg, Ag and Zn minor solute additions on the precipitation kinetics and strengthening of an Al-Cu-Li alloy

The influence of minor solute additions of Mg, Ag and Zn and their combinations on the precipitation kinetics and strengthening of an Al-Cu-Li alloy has been systematically investigated. Combining differential scanning calorimetry (DSC) and small-angle X-ray scattering (SAXS) provides information on how alloy chemistry changes the precipitation sequence, the precipitation kinetics in non – isothermal and in isothermal conditions, and the related strengthening. When adding Mg, the precipitation kinetics are strongly accelerated, which is shown to be related to the dominant formation of T1 precipitates. When adding Ag and Zn together with Mg, further enhancement of precipitation kinetics is observed, without change of the precipitation sequence, probably due to a more efficient nucleation of T1. The intrinsic strengthening potential of the T1 phase is shown to be unchanged by the addition of Ag and Zn, and the higher strength reached in the alloys containing these additions is shown to be due to a higher precipitate volume fraction.

Complementary Metal Oxide Semiconductor-Compatible, High-Mobility, ⟨111⟩-Oriented GaSb Nanowires Enabled by Vapor-Solid-Solid Chemical Vapor Deposition.

Using CMOS-compatible Pd catalysts, we demonstrated the formation of high-mobility ⟨111⟩-oriented GaSb nanowires (NWs) via vapor-solid-solid (VSS) growth by surfactant-assisted chemical vapor deposition through a complementary experimental and theoretical approach. In contrast to NWs formed by the conventional vapor-liquid-solid (VLS) mechanism, cylindrical-shaped Pd5Ga4 catalytic seeds were present in our Pd-catalyzed VSS-NWs. As solid catalysts, stoichiometric Pd5Ga4 was found to have the lowest crystal surface energy and thus giving rise to a minimal surface diffusion as well as an optimal in-plane interface orientation at the seed/NW interface for efficient epitaxial NW nucleation. These VSS characteristics led to the growth of slender NWs with diameters down to 26.9 ± 3.5 nm. Over 95% high crystalline quality NWs were grown in ⟨111⟩ orientation for a wide diameter range of between 10 and 70 nm. Back-gated field-effect transistors (FETs) fabricated using the Pd-catalyzed GaSb NWs exhibit a superior peak hole mobility of ∼330 cm2 V-1 s-1, close to the mobility limit for a NW channel diameter of ∼30 nm with a free carrier concentration of ∼1018 cm-3. This suggests that the NWs have excellent homogeneity in phase purity, growth orientation, surface morphology and electrical characteristics. Contact printing process was also used to fabricate large-scale assembly of Pd-catalyzed GaSb NW parallel arrays, confirming the potential constructions and applications of these high-performance electronic devices.

Investigation of nucleation processes during dynamic recrystallization of ice using cryo-EBSD.

Nucleation mechanisms occurring during dynamic recrystallization play a crucial role in the evolution of microstructures and textures during high temperature deformation. In polycrystalline ice, the strong viscoplastic anisotropy induces high strain heterogeneities between grains which control the recrystallization mechanisms. Here, we study the nucleation mechanisms occurring during creep tests performed on polycrystalline columnar ice at high temperature and stress (T=-5°C;σ=0.5 MPa) by post-mortem analyses of deformation microstructures using cryogenic electron backscatter diffraction. The columnar geometry of the samples enables discrimination of the nuclei from the initial grains. Various nucleation mechanisms are deduced from the analysis of the nuclei relations with the dislocation sub-structures within grains and at grain boundaries. Tilt sub-grain boundaries and kink bands are the main structures responsible for development of polygonization and mosaic sub-structures. Nucleation by bulging at serrated grain boundaries is also an efficient nucleation mechanism near the grain boundaries where strain incompatibilities are high. Observation of nuclei with orientations not related to the 'parent' ones suggests the possibility of 'spontaneous' nucleation driven by the relaxation of the dislocation-related internal stress field. The complexity of the nucleation mechanisms observed here emphasizes the impact of stress and strain heterogeneities on dynamic recrystallization mechanisms.This article is part of the themed issue 'Microdynamics of ice'.

Supramolecular Polymer Network-Mediated Self-Assembly of Semicrystalline Polymers with Excellent Crystalline Performance.

A novel application of supramolecular interactions within semicrystalline polymers, capable of self-assembling into supramolecular polymer networks via self-complementary multiple hydrogen-bonded complexes, is demonstrated for efficient construction of highly controlled self-organizing hierarchical structures to offer a direct, efficient nucleation pathway resulting in superior crystallization performance. Herein, a novel functionalized poly(ε-caprolactone) containing self-complementary sextuple hydrogen-bonded uracil-diamidopyridine (U-DPy) moieties is successfully developed and demonstrated excellent thermal and viscoelastic properties as well as high dynamic structural stability in the bulk state due to physical cross-linking created by reversible sextuple hydrogen bonding between U-DPy units. Due to the ability to vary the extent of the reversible network by tuning the U-DPy content, this newly developed material can be readily adjusted to obtain the desired crystalline products with specific characteristics. Importantly, incorporating only 0.1% U-DPy resulted in a polymer with a high crystallization rate constant, short crystallization half-time, and much more rapid crystallization kinetics than pristine PCL, indicating a low content of U-DPy moieties provides highly efficient nucleation sites that manipulate the nucleation and growth processes of polymer crystals to promote crystallization and chain alignment in bulk. This new system is suggested as a potential new route to substantially improve the performance of polymer crystallization.

Regulation of microtubule nucleation mediated by γ-tubulin complexes.

The microtubule cytoskeleton is critically important for spatio-temporal organization of eukaryotic cells. The nucleation of new microtubules is typically restricted to microtubule organizing centers (MTOCs) and requires γ-tubulin that assembles into multisubunit complexes of various sizes. γ-Tubulin ring complexes (TuRCs) are efficient microtubule nucleators and are associated with large number of targeting, activating and modulating proteins. γ-Tubulin-dependent nucleation of microtubules occurs both from canonical MTOCs, such as spindle pole bodies and centrosomes, and additional sites such as Golgi apparatus, nuclear envelope, plasma membrane-associated sites, chromatin and surface of pre-existing microtubules. Despite many advances in structure of γ-tubulin complexes and characterization of γTuRC interacting factors, regulatory mechanisms of microtubule nucleation are not fully understood. Here, we review recent work on the factors and regulatory mechanisms that are involved in centrosomal and non-centrosomal microtubule nucleation.

Investigation on the structural and optical properties of hexamethylene tetramine (HMTA) capped ZnS:Mn nanocrystals synthesized by microwave irradiation method

Monodispersed luminescent nanocrystals ZnS:Mn with and without hexamethylene tetramine (HMTA) as a capping agent were synthesized by microwave irradiation method and the influence of HMTA on the structural and optical properties were investigated. Remarkable stability was found in the case of surface-modified nanocrystals. Microwave synthesis method uniquely provides efficient and uniform nucleation. Zinc blend structure was observed for all the samples with particle size of 5.8 nm for uncapped and for capped it decreased (3.8-3.1 nm) with increase in the HMTA concentration. Influence of HMTA on the microstructure properties were discussed such as grain size, strain, dislocation density, lattice constant and texture coefficient. TEM images show spherical shape particles with size 10 nm (uncapped) and 4 nm (capped) nanocrystals. Blue shift with increase in the band gap was recorded. The yellow-orange emission peak related to Mn showed a blue shift for capped (585 nm) nanocrystals compared to that of uncapped nanocrystals (610 nm). Further increase in the peak intensity was observed with the increase in the capping agent concentration. Enhanced luminescence property was observed for capped ZnS:Mn2+ nanocrystals in comparison to uncapped. This type of capped semiconductor nanocrystals future can be extended in biological field because of the suitable capping agents which are capable of bonding with suitable bioagents.

Aesthetically improved and efficient tannin–metal chelates for the treatment of dentinal hypersensitivity

Tannin–metal chelates for the efficient nucleation of hydroxyapatite and an aesthetically improved solution for the dentinal hypersensitivity treatment.

A DFT study of the interaction between large PAHs and atomic chlorine or hydrogen chloride molecule: Toward a modelling of the influence of chlorinated species on the trapping of water by soot

First-principle calculations have been performed to characterize the interaction of chlorinated species (HCl and Cl) with large polycyclic aromatic hydrocarbon (PAH) molecules and radicals. Whereas the characterization of the interaction process on the face of the PAH molecules requires taking into account long-range dispersion interactions in the calculations, trapping at the edge of PAH radicals involves stronger interactions that lead to the dissociation of the HCl molecule. Then, the first steps of water adsorption on the corresponding chlorinated species has been characterized, showing that chlorine may act as an efficient nucleation center for water molecules on such aromatic systems mimicking part of the carbonaceous surfaces that are likely present in soot. These results represent a first but necessary step for a better understanding of soot behavior in industrial or domestic fire situations.