58 research outputs found
Ab initio investigation of the crystallization mechanism of cadmium selenide
Cadmium selenide (CdSe) is an inorganic semiconductor with unique optical and
electronic properties that made it useful in various applications, including
solar cells, light-emitting diodes, and biofluorescent tagging. In order to
synthesize high-quality crystals and subsequently integrate them into devices,
it is crucial to understand the atomic scale crystallization mechanism of CdSe.
Unfortunately, such studies are still absent in the literature.To overcome this
limitation, we employed an enhanced sampling-accelerated active learning
approach to construct a deep neural potential with ab initio accuracy for
studying the crystallization of CdSe.Our brute-force molecular dynamics
simulations revealed that a spherical-like nucleus formed spontaneously and
stochastically, resulting in a stacking disordered structure where the
competition between hexagonal wurtzite and cubic zinc blende polymorphs is
temperature-dependent. We found that pure hexagonal crystal can only be
obtained approximately above 1430 K, which is 35 K below its melting
temperature. We observed that the solidification dynamics of Cd and Se atoms
were distinct due to their different diffusion coefficients. The solidification
process was initiated by lower mobile Se atoms forming tetrahedral frameworks,
followed by Cd atoms occupying these tetrahedral centers and settling down
until the third-shell neighbor of Se atoms sited on their lattice positions.
Therefore, the medium-range ordering of Se atoms governs the crystallization
process of CdSe. Our findings indicate that understanding the complex dynamical
process is the key to comprehending the crystallization mechanism of compounds
like CdSe, and can shed lights in the synthesis of high-quality crystals.Comment: 25 pages, 7 figure
MicroRNA-145-5p Regulates the Epithelial-Mesenchymal Transition in Nasal Polyps by Targeting Smad3
Objectives. The annual prevalence of chronic rhinosinusitis (CRS) is increasing, and the lack of effective treatments imposes a substantial burden on both patients and society. The formation of nasal polyps in patients with CRS is closely related to tissue remodeling, which is largely driven by the epithelial-mesenchymal transition (EMT). MicroRNA (miRNA) plays a pivotal role in the pathogenesis of numerous diseases through the miRNA-mRNA regulatory network; however, the specific mechanism of the miRNAs involved in the formation of nasal polyps remains unclear. Methods. The expression of EMT markers and Smad3 were detected using western blots, quantitative real-time polymerase chain reaction, and immunohistochemical and immunofluorescence staining. Differentially expressed genes in nasal polyps and normal tissues were screened through the Gene Expression Omnibus database. To predict the target genes of miR-145-5p, three different miRNA target prediction databases were used. The migratory ability of cells was evaluated using cell migration assay and wound healing assays. Results. miR-145-5p was associated with the EMT process and was significantly downregulated in nasal polyp tissues. In vitro experiments revealed that the downregulation of miR-145-5p promoted EMT. Conversely, increasing miR-145-5p levels reversed the EMT induced by transforming growth factor-β1. Bioinformatics analysis suggested that miR-145-5p targets Smad3. Subsequent experiments confirmed that miR-145-5p inhibits Smad3 expression. Conclusion. Overall, miR-145-5p is a promising target to inhibit nasal polyp formation, and the findings of this study provide a theoretical basis for nanoparticle-mediated miR-145-5p delivery for the treatment of nasal polyps
The conservation and uniqueness of the caspase family in the basal chordate, amphioxus
<p>Abstract</p> <p>Background</p> <p>The caspase family, which plays a central role in apoptosis in metazoans, has undergone an expansion in amphioxus, increasing to 45 members through domain recombination and shuffling.</p> <p>Results</p> <p>In order to shed light on the conservation and uniqueness of this family in amphioxus, we cloned three representative caspase genes, designated as <it>bbtCaspase-8, bbtCaspase-1/2 </it>and <it>bbtCaspase3</it>-like, from the amphioxus <it>Branchiostoma belcheri tsingtauense</it>. We found that <it>bbtCaspase-8 </it>with conserved protein architecture is involved in the Fas-associated death domain-Caspase-8 mediated pro-apoptotic extrinsic pathway, while <it>bbtCaspase3</it>-like may mediate a nuclear apoptotic pathway in amphioxus. Also, <it>bbtCaspase-1/2 </it>can co-localize with <it>bbtFADD2 </it>in the nucleus, and be recruited to the cytoplasm by amphioxus apoptosis associated speck-like proteins containing a caspase recruitment domain, indicating that <it>bbtCaspase-1/2 </it>may serve as a switch between apoptosis and caspase-dependent innate immune response in invertebrates. Finally, amphioxus extrinsic apoptotic pathway related caspases played important roles in early embryogenesis.</p> <p>Conclusions</p> <p>Our study not only demonstrates the conservation of <it>bbtCaspase-8 </it>in apoptosis, but also reveals the unique features of several amphioxus caspases with novel domain architectures arose some 500 million years ago.</p
Reactant-Induced Dynamics of Lithium Imide Surfaces during the Ammonia Decomposition Process
Ammonia decomposition on lithium imide surfaces has been intensively investigated owing to its potential role in a sustainable hydrogen-based economy. Through advanced molecular dynamics simulations of ab initio accuracy, we show that the surface structure of the catalyst changes upon exposure to the reactants, and a new dynamic state is activated. It is this highly fluctuating state that is responsible for catalysis and not a well defined static catalytic center. In this activated environment, a series of reactions that eventually leads to the release of N2 and H2 molecules become possible. Once the flow of reagent is terminated the imide surface returns to its pristine state. We suggest that by properly engineering this dynamic interfacial state one can design improved catalytic systems
Three-Dimensional Device-Free Localization for Vehicle
Device-free localization (DFL) is a promising technique which could provide localization information for a target without requiring an electronic device. With the development of the smart city and smart transportation, DFL could form part of a basic technique that could be used to track and localize roadside vehicles. In this paper, some algorithms for three-dimensional (3D) DFL for vehicle surveillance are developed, including statistical methods for data, a method for communication link selection, a novel method of communication link weight allocation and some other minor approaches to obtain the location and approximate size of a static vehicle, as a basic technique of moving vehicle detection. Then, an experimental system is designed. Through security monitoring wireless sensor networks (WSN), real-time vehicle characteristics (i.e., location and size) are calculated automatically and intuitively displayed through a heat map. Experiments are performed to validate the effect of the proposal and the accuracy of the localization and size estimation
Ultrasmall Fe<sub>2</sub>O<sub>3</sub> Tubular Nanomotors: The First Example of Swarming Photocatalytic Nanomotors Operating in High-Electrolyte Media
Self-propelled chemical micro/nanomotors (MNMs) have demonstrated considerable potential in targeted drug delivery, (bio)sensing, and environmental remediation due to their autonomous nature and possible intelligent self-targeting behaviors (e.g., chemotaxis and phototaxis). However, these MNMs are commonly limited by their primary propulsion mechanisms of self-electrophoresis and electrolyte self-diffusiophoresis, making them prone to quenching in high electrolyte environments. Thus, the swarming behaviors of chemical MNMs in high-electrolyte media remain underexplored, despite their potential to enable the execution of complex tasks in high-electrolyte biological media or natural waters. In this study, we develop ultrasmall tubular nanomotors that exhibit ion-tolerant propulsions and collective behaviors. Upon vertical upward UV irradiation, the ultrasmall Fe2O3 tubular nanomotors (Fe2O3 TNMs) demonstrate positive superdiffusive photogravitaxis and can further self-organize into nanoclusters near the substrate in a reversible manner. After self-organization, the Fe2O3 TNMs exhibit a pronounced emergent behavior, allowing them to switch from random superdiffusions to ballistic motions near the substrate. Even at a high electrolyte concentration (Ce), the ultrasmall Fe2O3 TNMs retain a relatively thick electrical double layer (EDL) compared to their size, and the electroosmotic slip flow in their EDL is strong enough to propel them and induce phoretic interactions among them. As a result, the nanomotors can rapidly concentrate near the substrate and then gather into motile nanoclusters in high-electrolyte environments. This work opens a gate for designing swarming ion-tolerant chemical nanomotors and may expedite their applications in biomedicine and environmental remediation
How Does Structural Disorder Impact Heterogeneous Catalysts? The Case of Ammonia Decomposition on Non-Stoichiometric Lithium Imide
Among the many catalysts suggested for ammonia decomposition, Li2NH has been shown to be quite promising. In the recent past, we have performed extensive \textit{ab-initio}-quality simulations to explain the workings of this unusual catalyst. In the complex scenario that has emerged, surface dynamics and structural disorder enhanced by the interaction with the reacting ammonia molecules played a crucial role. Non-stoichiometric lithium imide Li(2-x)(NH2)x(NH)(1-x) has been reported to have better catalytic performances than pure lithium imide. Stimulated by these findings, we follow up our first study simulating the ammonia decomposition on such non-stoichiometric compound. We attribute the enhanced reactivity to the fact that the compositional disorder further enhances the fluctuations in the topmost layers of the catalyst, strengthening our dynamical picture of this catalytic process
Dual-Band Sensor Network for Accurate Device-Free Localization in Indoor Environment with WiFi Interference
International audienceRadio Frequency based Device-Free Localization (RFDFL) is an emerging localization technique without requirements of attaching any electronic device to a target. The target can be localized by means of measuring the shadowing of received signal strength caused by the target. However, the accuracy of RFDFL deteriorates seriously in environment with WiFi interference. State-of-the-art methods do not efficiently solve this problem. In this paper, we propose a dual-band method to improve the accuracy of RFDFL in environment without/with severe WiFi interference. We introduce an algorithm of fusing dual-band images in order to obtain an enhanced image inferring more precise location and propose a timestamp-based synchronization method to associate the dual-band images to ensure their one-one correspondence. With real-world experiments, we show that our method outperforms traditional single-band localization methods and improves the localization accuracy by up to 40.4% in real indoor environment with high WiFi interference
Resveratrol enhances anticancer effects of paclitaxel in HepG2 human liver cancer cells
Abstract Background The aim of this in vitro study was to measure the enhanced anticancer effects of Res (resveratrol) on PA (paclitaxel) in HepG2 human liver cancer cells. Methods The MTT (thiazolyl blue tetrazolium bromide, 3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide), flow cytometry, qPCR (real-time quantitative polymerase chain reaction) and western blot assay were used for cells growth inhibitory effects, cells apoptosis (DNA content of sub-G1), mRNA and protein expressions, respectively. Results The 10 μg/mL of Res had no growth inhibitory effect on Nthy-ori 3–1 normal cells or HepG2 cancer cells meanwhile the 5 or 10 μg/mL of PA also had no growth inhibitory effect on Nthy-ori 3–1 normal cells. Where as PA-L (5 μg/mL) and PA-H (10 μg/mL) had the growth inhibitory effects in HepG2 cancer cells, and Res increase these growth inhibitory effects. By flow cytometry experiment, after Res (5 μg/mL) + PA-H (10 μg/mL) treatment, the HepG2 cells showed the most apoptosis in cells as compared to other treatments groups, and after additionally treated with Res, both the apoptosis cells of two concentrations PA were raised. As PA raised it also raised the mRNA and protein expressions of caspase-3, caspase-8, caspase-9, Bax (Bcl-2 assaciated X protein), p53, p21, IκB-α (inhibitor of NF-κB alpha), Fas (factor associated suicide), FasL (factor associated suicide ligand), TIMP-1 (tissue inhibitor of metalloproteinases 1), TIMP-2 (tissue inhibitor of metalloproteinases 2) and decrease Bcl-2 (B cell leukemia 2), Bcl-xL (B cell leukemia extra large), HIAP-1 (cIAP-1, cellular inhibitor of apoptosis 1), HIAP-2 (cIAP-2, cellular inhibitor of apoptosis 2), NF-κB (nuclear factor kappa B), COX-2 (cyclooxygenase 2), iNOS (inducible nitric oxide synthase), MMP-2 (metalloproteinase 2), MMP-9 (metalloproteinase 9), EGF (epidermal growth factor), EGFR (epidermal growth factor receptor), VEGF (vascular endothelial growth factor), Fit-1 (VEGFR-1, vascular endothelial growth factor receptor 1). Meanwhile, the 5 μg/mL of Res could enhance these mRNA expressions changes as compared to the control cells. Conclusion From these results, we can conclude that Res could raise the anticancer effects of PA in HepG2 cells, Res could be used as a good sensitizing agent for PA
How Does Structural Disorder Impact Heterogeneous Catalysts? The Case of Ammonia Decomposition on Non-stoichiometric Lithium Imide
Among the many catalysts suggested for ammonia decomposition,
Li2NH has been shown to be quite promising. In the recent
past,
we have performed extensive ab initio-quality simulations
to explain the workings of this unusual catalyst. In the complex scenario
that has emerged, surface dynamics and structural disorder enhanced
by the interaction with the reacting ammonia molecules have played
crucial roles. Non-stoichiometric lithium imide (Li2–x(NH2)x(NH)1–x) has been reported to have better
catalytic performances than pure lithium imide. Stimulated by these
findings, we follow up our previous study simulating the ammonia decomposition
on such non-stoichiometric compounds. We attribute the enhanced reactivity
to the fact that the compositional disorder further enhances the fluctuations
in the topmost layers of the catalyst, strengthening our dynamic picture
of this catalytic process
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