Search Results (144)

Based on the excellent performance of the K(Ta_0.5Nb_0.5)O₃ (KTN) system, this study systematically investigated the mechanism of the influence of metal element (Cd, Sn, Hf) doping on the photocatalytic performance of KTN ferroelectric materials using the density functional theory (DFT) based on first principles. The findings indicate that after metal atom doping, the tolerance factor of doping systems is similar to that of pure KTN crystals, confirming that doping does not compromise its structural stability. However, the ion radius differences caused by doping lead to lattice distortion, significantly reducing the bandgap width. Because the impurity element substituting the Ta site exhibits a lower valence state compared to Ta, holes become the majority carriers, thereby endowing the semiconductor with p-type characteristics. These characteristics effectively suppress electron–hole recombination while enhancing electron transitions. Furthermore, the increase in the dielectric constant of the doped system indicates an enhancement in its polarization capability, which is accompanied by a significant improvement in carrier mobility. The peak of the imaginary part of the dielectric function and the peak of the absorption spectrum both shift towards the low-energy region, indicating that doping has expanded the light response range of the system. Moreover, the effective mass of the holes in all doped systems is significantly higher than that of the electrons, further demonstrating that the introduction of impurities is conducive to hindering the separation of photogenerated electron–hole pairs. These modifications significantly enhance the photocatalytic performance of the systems. Full article

The development of gas sensors with high sensitivity and low operating temperatures is essential for practical applications in environmental monitoring and industrial safety. SnO₂-based gas sensors, despite their widespread use, often suffer from high working temperatures and limited sensitivity to H₂ gas, which presents significant challenges for their performance and application. This study addresses these issues by introducing a novel SnO₂-based sensor featuring a three-dimensional (3D) nanostructure, designed to enhance sensitivity and allow for room-temperature operation. This work lies in the use of a 3D anodic aluminum oxide (AAO) template to deposit SnO₂ nanoparticles through ultrasonic spray pyrolysis, followed by modification with platinum (Pt) nanoparticles to further enhance the sensor’s response. The as-prepared sensors were extensively characterized, and their H₂ sensing performance was evaluated. The results show that the 3D nanostructure provides a uniform and dense distribution of SnO₂ nanoparticles, which significantly improves the sensor’s sensitivity and repeatability, especially in H₂ detection at room temperature. This work demonstrates the potential of utilizing 3D nanostructures to overcome the traditional limitations of SnO₂-based sensors. Full article

Background: snoRNAs have traditionally been known for their role as guides in post-transcriptional rRNA modifications. Previously, our research group identified several RNAs that may bind to PIP2 with LIPRNA-seq. Among them, snR191 stood out due to its potential specific interaction with this lipid, distinguishing itself from other snoRNAs. However, a detailed study is needed to define the molecular interactions between RNA and lipids, which remain unknown but may serve as a mechanism for transport or liquid–liquid phase separation. This study aimed to determine the interaction between a snoRNA called snR191 and PIP2. Method: A novel methodology for RNA-PIP2 interaction was carried out. Total RNA from Saccharomyces cerevisiae was incubated with PIP2-bound nitrocellulose membranes and RT-PCR reactions. We performed the prediction of snR191-PIP2 interaction by molecular docking and in silico mutations of snoR191. Results: From LIPRNA-seq analysis, we identified that PIP2-bound RNAs were significantly enriched in diverse biological processes, including transmembrane transport and redox functions. Our RNA-PIP2 interaction approach was successful. We demonstrated that snR191 specifically interacts with PIP2 in vitro. The elimination of DNA ensured that the interaction assay was RNA-specific, strengthening the robustness of the experiment. PIP2 was docked to snR191 in a stem–loop–stem motif. Six hydrogen bonds across four nucleotides mediated the PIP2-snR191 interaction. Finally, mutations in snR191 affected the structural folding. Conclusions: In this study, we demonstrate the effectiveness of a new methodology for determining RNA–lipid interactions, providing strong evidence for the specific interaction between snR191 and PIP2. Integrating biochemical and computational approaches has allowed us to understand the binding of these biomolecules. Therefore, this work significantly broadens our understanding of snR191-PIP2 interactions and opens new perspectives for further research. Full article

Background/Objectives: Cancer research aims to understand the cellular and molecular mechanisms involved, in order to identify new therapeutic targets and provide patients with more effective therapies that generate fewer side undesirable and toxic effects. Previous studies have demonstrated the role of small nucleolar RNAs (snoRNAs) in many physiological and pathological cellular processes, including cancers. SnoRNAs are a group of non-coding RNAs involved in different post-transcriptional modifications of ribosomal RNAs. Recently, we identified a new snoRNA (jouvence), first in Drosophila, and thereafter, by homology, in humans. Methods: Here, we characterize the effect of the knockdown of jouvence by a sh-lentivirus on human primary patient-derived glioblastoma cells. Results: The sh-lentivirus anti-jouvence induces a significant decrease in cell proliferation and leads to cell death. EdU staining confirmed this decrease, while TUNEL also showed the presence of apoptotic cells. An RNA-Seq analysis revealed a decrease, in particular, in the level of BAALC, a gene known to potentiate the oncogenic ERK pathway and deregulating p21, leading to cell cycle blockage. Conclusions: Altogether, these results allow the hypothesis that the knockdown of jouvence could potentially be used as a new anti-cancer treatment (sno-Therapy), especially against glioblastoma and also, potentially, against acute myeloid leukemia (AML) due to the BAALC deregulation. Full article

This paper presents the results of an investigation into the catalytic activity and selectivity of rhodium-based catalysts supported on natural zeolite clinoptilolite from the Shankanai field (Kazakhstan) in the dehydrogenation of light alkanes from associated petroleum gas (APG). Three modifications of the catalyst have been studied: basic 1%Rh/HCpt, modified with tin 1%Rh/10%SnO/HCpt, and combined with additives of tin and potassium 1%Rh/10%SnO/5%K₂O/HCpt. It has been shown that the addition of tin contributes to increased thermal stability and a decreased coking rate, while the addition of potassium suppresses side reactions (cracking and isomerization), increasing the selectivity for olefins. The highest yield of olefins (~30%) is achieved with the 1%Rh/10%SnO/5%K₂O/HCpt catalyst in the presence of water vapor. Using scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM), improved distribution of active components and reduced catalyst deactivation have been confirmed. The obtained data demonstrate the potential of the developed systems for the efficient processing of APG and the selective synthesis of olefins. Full article

Nitric oxide (NO) can perform its physiological role through protein S-nitrosylation, a redox-based post-translational modification (PTM). This review details the specific molecular mechanisms and current detection technologies of S-nitrosylation. It also comprehensively synthesizes emerging evidence of S-nitrosylation roles in plant biological processes, including growth and development, immune signaling, stress responses and symbiotic nitrogen fixation. Furthermore, the review analyzes research progress on the crosstalk between S-nitrosylation and other protein PTMs. Finally, unresolved issues such as the spatio-temporal resolution of SNO-proteome mapping and standardized protocols for reproducibility are pointed out. In summary, this work proposes a roadmap for future research. Full article

Notwithstanding the success of SnO₂ as a fundamental material for gas sensing, it has often been criticized for its cross-sensitivity and high operational temperatures. Therefore, in this study, RF-sputtered SnO₂ thin films were subjected to a modification process through doping with a rare earth element, dysprosium (Dy), and subsequently deposited onto two different types of substrates: alumina and glass substrates. All thin films underwent a comprehensive series of characterizations aimed at ensuring their suitability as NO₂ sensors. The dysprosium doping levels ranged from 1 to 7 wt.% in increments of 2% (wt.%). X-ray patterns showed that all deposited films exhibited the tetragonal rutile structure of SnO₂. The optical band gap energy (Eg) increased with Dy doping, while the Urbach energy decreased with Dy doping. Field emission scanning electron microscopy (FESEM) revealed highly compacted grainy surfaces with high roughness for alumina substrate thin films, which also exhibited higher resistivity that increased with the levels of Dy doping. Energy-dispersive X-ray spectroscopy (EDX) analyses confirmed the stoichiometry of both types of thin films. Gas sensing tests were conducted at different operating temperatures, where the highest response to nitrogen dioxide, over 42%, was recorded for the higher dopant level at 250 °C. Moreover, the sensor’s selectivity toward nitrogen dioxide traces was evaluated by introducing interfering gases at higher concentrations. However, the sensors showed also significant responses when operated at room temperature. Also, we have demonstrated that higher stability is related to the temperature of the sensors and Dy ratio. Hence, a detailed discussion of the gas-sensing mechanisms was undertaken to gain a deeper insight into the NO₂ sensitivity exhibited by the Dy-doped SnO₂ layer. Full article

To overcome the limitations of conventional catalysts in sterically hindered esterification reactions, a radio frequency (RF) plasma-modified $\mathrm{S}{\mathrm{O}}_4^{2-}$/${\mathrm{S}}_2{\mathrm{O}}_8^{2-}$/SnO₂-Al₂O₃ solid superacid catalyst was synthesized via sol-gel and impregnation, followed by RF plasma treatment and calcination. Comprehensive characterization revealed that the RF plasma modification endowed the catalyst with a uniform particle distribution (4.32 nm average size), larger specific surface area (104.44 m²·g⁻¹), elevated total acid content (142.86 μmol·g⁻¹), and increased oxygen vacancy concentration (16.4%), compared to the conventional sol-gel–impregnation–calcination-prepared catalyst. The RF plasma-modified $\mathrm{S}{\mathrm{O}}_4^{2-}$-${\mathrm{S}}_2{\mathrm{O}}_8^{2-}$/SnO₂-Al₂O₃ was subsequently applied to perform the esterification reaction of Tyr, with a higher steric hindrance. Mechanistic studies indicated that the plasma-induced surface etching and electronic redistribution/intensified electron-withdrawing capability of $\mathrm{S}{\mathrm{O}}_4^{2-}$/${\mathrm{S}}_2{\mathrm{O}}_8^{2-}$ groups synergistically strengthened Brønsted/Lewis acidity. For the esterification of tyrosine—a sterically demanding substrate—the modified catalyst achieved a 92.1% methyl tyrosine yield under the optimized conditions (180 °C, 0.8 MPa N₂, 6 h), where the catalyst exhibited a better mechanical strength and better lifetime with five cycles. This work not only provides a scalable plasma-assisted strategy for tuning solid superacids but also establishes an eco-friendly alternative to traditional catalysts, and was applied to the esterification reactions of some high-steric-hindrance substrates. Full article

SnO₂-based semiconductor gas-sensing materials are regarded as some of the most crucial sensing materials, owing to their extremely high electron mobility, high sensitivity, and excellent stability. To bridge the gap between laboratory-scale SnO₂ and its industrial applications, low-cost and high-efficiency requirements must be met. This implies the need for simple synthesis techniques, reduced energy consumption, and satisfactory gas-sensing performances. In this study, we utilized a surfactant-free simple method to modify SnO₂ nanoparticles with PdPt noble metals, ensuring the stable state of the material. Under the synergistic catalytic effect of Pd and Pt, the composite material (1.0 wt%-PdPt-SnO₂) significantly enhanced its response to HCHO. This modification decreased the optimal working temperature to as low as 180 °C to achieve a response value (R_a/R_g = 8.2) and showcased lower operating temperatures, higher sensitivity, and better selectivity to detect 10 ppm of HCHO when compared with pristine SnO₂ or single noble metal-decorated SnO₂ sensors. Stability tests verified that the gas sensor signals based on PdPt-SnO₂ nanoparticles exhibit good reliability. Furthermore, a portable HCHO detector was designed for practical applications, such as in newly purchased cushions, indicating its potential for industrialization beyond the laboratory. Full article

Translation regulation is essential to the survival of hosts. Most translation initiation falls under the control of the mTOR pathway, which regulates protein production from mono-methyl-guanosine (m7G) cap mRNAs. However, mTOR does not regulate all translation; hosts and viruses alike employ alternative pathways, protein factors, and internal ribosome entry sites to bypass mTOR. Trimethylguanosine (TMG)-caps arise from hypermethylation of pre-existing m7G-caps by the enzyme TGS1 and are modifications known for snoRNA, snRNA, and telomerase RNA. New findings originating from HIV-1 research reveal that TMG-caps are present on mRNA and license translation via an mTOR-independent pathway. Research has identified TMG-capping of selenoprotein mRNAs, junD, TGS1, DHX9, and retroviral transcripts. TMG-mediated translation may be a missing piece for understanding protein synthesis in cells with little mTOR activity, including HIV-infected resting T cells and nonproliferating cancer cells. Viruses display a nuanced interface with mTOR and have developed strategies that take advantage of the delicate interplay between these translation pathways. This review covers the current knowledge of the TMG-translation pathway. We discuss the intimate relationship between metabolism and translation and explore how this is exploited by HIV-1 in the context of CD4+ T cells. We postulate that co-opting both translation pathways provides a winning strategy for HIV-1 to dictate the sequential synthesis of its proteins and balance viral production with host cell survival. Full article

Protein S-nitrosation, a redox post-translational modification elicited by nitric oxide (NO), is essential for modulating diverse protein functions and signaling pathways. Dysregulation of S-nitrosation is implicated in various pathological processes, including oxygen-glucose deprivation/reperfusion (OGD/R) injury, a widely used model for ischemia-reperfusion diseases. The dynamic changes in S-nitrosothiols (SNOs) during ischemia-reperfusion highlight the need for theranostic strategies to monitor and modulate SNO levels based on pathological progression. However, to date, no theranostic strategies have been reported for addressing dysregulated SNO in disease models, particularly in OGD/R conditions. Here, we report the development of a selective probe P-EHC, which could specifically react with SNOs to release EHC, not only exhibiting turn-on fluorescence with high quantum yield and good water solubility but also demonstrating macrophage migration inhibitory factor (MIF) inhibitory activity. In an OGD/R model of SH-SY5Y cells, we observed elevated SNO levels by using live-cell confocal imaging. Treatment of P-EHC significantly reduced intracellular reactive oxygen species (ROS), lowered total NO_x species, and improved cell viability in the OGD/R model. In summary, the simplicity and versatility of P-EHC suggest its broad applicability for monitoring SNO in various biological models and therapeutic contexts, particularly in ischemia-reperfusion diseases. Full article

The emission of toxic gases such as NO₂, NO, SO₂, and CO from industrial activities, transportation, and energy production poses significant threats to the environment and public health. Traditional gas sensors often lack high sensitivity and selectivity. To address this, our study uses first-principles density functional theory (DFT) to investigate CuO-SnS monolayers for improved gas sensor performance. The results show that CuO modification significantly enhances the adsorption capacity and selectivity of SnS monolayers for NO₂ and NO, with adsorption energies of −2.301 eV and −2.142 eV, respectively. Furthermore, CuO modification is insensitive to CO₂ adsorption, demonstrating excellent selectivity. Structural and electronic analyses reveal that CuO modification reduces the band gap of SnS monolayers from 1.465 eV to 0.635 eV, improving the electrical conductivity and electron transfer, thereby enhancing the gas adsorption sensitivity. Further analyses highlight significant electronic interactions and charge transfer mechanisms between CuO-SnS monolayers and NO₂ and SO₂ molecules, indicating strong orbital hybridization. In conclusion, this study provides a theoretical basis for developing high-performance gas sensors, showing that CuO-SnS monolayers have great potential for detecting toxic gases. Full article

In this study, a TiO₂/(MA)₂SnCl₄ nanocomposite film was synthesized using a sustainable, sunlight-driven approach, demonstrating enhanced photocatalytic performance for environmental remediation. TiO₂ nanoparticles (TiO₂-NPs) were dispersed in ethanol and mixed with a methylammonium (MA) and SnCl₂ precursor solution, followed by drop-casting onto a glass substrate and exposure to direct sunlight for 2 h. Sunlight served as an energy source, facilitating in situ structural modifications and leading to the formation of a well-integrated TiO₂/(MA)₂SnCl₄ hybrid structure, where TiO₂ was effectively encapsulated. Characterization revealed a band gap reduction from 3.1 eV (TiO₂-NPs) to 2.6 eV in the nanocomposite, extending light absorption into the visible range. The formation of Sn–O–Ti interactions enhanced charge separation, minimized electron–hole recombination, and improved charge carrier dynamics. Photocatalytic degradation tests using methylene blue (MB) under sunlight showed that the nanocomposite film achieved 90% MB degradation within 60 min, outperforming TiO₂-NPs, which achieved only 75% degradation. The presence of oxygen vacancies (OVs) generated during sunlight exposure further enhanced photocatalytic efficiency by acting as charge traps and reaction sites. This study introduces a green synthesis strategy leveraging sunlight as a renewable energy source, marking the first integration of (MA)₂SnCl₄ with TiO₂-NPs for enhanced photocatalysis. The synergistic effects of extended visible-light absorption, defect engineering, and efficient charge separation make TiO₂/(MA)₂SnCl₄ nanocomposite films a scalable, cost-effective solution for water purification applications, offering a promising solar-driven approach to addressing global water contamination challenges. Full article

Sn-doped TiO₂–carbon composites were identified as promising multifunctional supports for Pt electrocatalysts, in which the oxide component enhances resistance against corrosion and strong metal–support interactions at the Pt-oxide boundary ensure high stability for the Pt nanoparticles. This work is devoted to the study of the influence of preliminary functionalization of the carbon on the properties of Pt/Ti_0.9Sn_0.1O₂–C catalysts. The structural, compositional and morphological differences between the samples prepared using functionalized or unmodified carbon, as well as the effect of carbon pre-modification on the electrocatalytic behavior of the synthesized Pt catalysts, were investigated using TEM, XRD, XPS, nitrogen adsorption and electrochemical measurements. The presence of oxygen-containing functional groups on carbon treated with HNO₃ and glucose leads to the formation of a homogeneous coating of the carbon with dispersed crystallites of mixed oxide. Elemental mapping revealed the proximity of Sn species with highly dispersed (2–3 nm) Pt particles. Notably, the electrochemical results indicated enhanced activity in CO electrooxidation for both functionalized and unmodified carbon-containing catalysts. An improvement in the 10,000-cycle long-term stability of the catalyst prepared using functionalized carbon was evident compared to the catalyst with untreated carbon or reference Pt/C. Full article

This review gives an overview of Si-, Ge- and Sn-compounds with (O,N)-bi- and -oligodentate ligands, which have the α-amino carboxylic acid motif N–C(R,R′)–C(=O)O in common (R,R′ = H or hydrocarbyl). While the amino acids themselves are encountered as mono- and di-anionic ligands, modifications at the N-terminus (e.g., extension of the ligand backbone by, e.g., additional alkane carboxylic acid groups) give rise to a wealth of ligands, which bear the α-amino carboxylic acid motif. With particular interest in the coordination features of these ligands, crystallographically characterized complexes are the focus of this review. Full article