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Glioblastoma multiforme (GBM) is the most prevalent and aggressive brain tumor found in adult humans with a poor prognosis and average survival of 14-15 months. In order to have a comprehensive understanding of proteome and identify novel therapeutic targets, this study focused mainly on the differentially abundant proteins (DAPs) of Ras V12 -induced GBM. Ras V12 is a constitutively active Ras mutant form essential for tumor progression by continuously activating signaling pathways leading to uncontrolled tumor growth. This study used a transgenic Drosophila model with Ras V12 overexpression using the repo-GAL4 driver line, specifically in glial cells, to study GBM. The high-resolution mass spectrometry (HRMS)-based proteomic analysis of the GBM larval central nervous system identified three novel DAPs specific to mitochondria. These DAPs, probable maleylacetoacetate isomerase 2 (Q9VHD2), bifunctional methylene tetrahydrofolate dehydrogenase (Q04448), and glutamine synthetase1 (P20477), identified through HRMS were further validated by qRT-PCR. The protein-protein interaction analysis revealed interactions between Ras V12 and DAPs, with functional links to mitochondrial dynamics regulators such as Drp1, Marf, Parkin, and HtrA2. Notably, altered expressions of Q9VHD2, P20477, and Q04448 were observed during GBM progression, which offers new insights into the involvement of mitochondrial dynamic regulators in Ras V12 -induced GBM pathophysiology.

Transition-metal dichalcogenides (TMDs) have long been attractive to researchers for their diverse properties and high degree of tunability. Most recently, interest in magnetically intercalated TMDs has resurged due to their potential applications in spintronic devices. While certain compositions featuring the absence of inversion symmetry such as Fe 1/3 NbS 2 and Cr 1/3 NbS 2 have garnered the most attention, the diverse compositional space afforded through the host matrix composition as well as intercalant identity and concentration is large and remains relatively underexplored. Here, we report the magnetic ground state of Fe 1/4 NbS 2 that was determined from low-temperature neutron powder diffraction as an A-type antiferromagnet. Despite the presence of overall inversion symmetry, the pristine compound manifests spin polarization induced by the antiferromagnetic order at generic k points, based on density functional theory band-structure calculations. Furthermore, by combining synchrotron diffraction, pair distribution function, and magnetic susceptibility measurements, we find that the magnetic properties of Fe 1/4 NbS 2 are sensitive to the Fe site order, which can be tuned via electrochemical lithiation and thermal history.

Carbon dioxide (CO 2 ), a valuable feedstock, can be reutilized as a hydrogen carrier by hydrogenating CO 2 to formic acid (FA) and releasing hydrogen by FA dehydrogenation in a reversible manner. Notably, FA is liquid at room temperature and can be stored and transported considerably more safely than hydrogen gas. Herein, we extensively reviewed transition-metal-based molecular catalysts explored for reversible CO 2 hydrogenation and FA dehydrogenation. This Review describes different approaches explored for carbon-neutral hydrogen storage and release by applying CO 2 hydrogenation to FA/formate and the subsequent release of H 2 by the dehydrogenation of FA over a wide range of molecular catalysts based on noble and non-noble metals. Emphasis is also placed on the specific catalyst-to-substrate interaction by highlighting the specific role of the catalyst in the CO 2 hydrogenation-FA dehydrogenation pathway., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

Diruthenium complexes [{(η 6 -arene)RuCl} 2 (μ-κ 2 :κ 2 -benztetraimd)] 2+ containing the bridging bis-imidazole methane-based ligand {1,4-bis(bis(2-ethyl-5-methyl-1 H -imidazol-4-yl)methyl)benzene} (benztetraimd) are synthesized for catalytic formic acid dehydrogenation in water at 90 °C. Catalyst [{(η 6 - p -cymene)RuCl} 2 (μ-κ 2 :κ 2 -benztetraimd)] 2+ [1-Cl 2 ] exhibited a remarkably high turnover frequency (1993 h -1 per Ru atom) and long-term stability over 60 days for formic acid dehydrogenation, while the analogous (η 6 -benzene)diruthenium and mononuclear catalysts displayed low activity with poor long-term stability. Notably, catalyst [1-Cl 2 ] also displayed an appreciably high turnover number of 93 200 for the bulk-scale reaction. In addition, the in-depth mass and nuclear magnetic resonance investigations under the catalytic and control experimental conditions revealed the active involvement of several crucial catalytic intermediate species, such as Ru-aqua species [{(η 6 - p -cymene)Ru(H 2 O)} 2 (μ-L)] 2+ [1-(OH 2 ) 2 ] , Ru-formato species [{(η 6 - p -cymene)Ru(HCOO)} 2 (μ-L)] [1 - (HCOO) 2 ] , and Ru-hydrido species [{(η 6 - p -cymene)Ru(H)} 2 (μ-L)] [1-(H) 2 ] , in the catalytic formic acid dehydrogenation reaction.

The current study addresses the generation of surface-modified nanograined anatase (5 nm) by a single-step in situ process. The EDTA-diol (ester) functionality existing on the surface of anatase nanoparticles was proved with the help of a battery of physicochemical techniques, including FTIR, XPS, and NMR spectral measurements. The sample showed excellent dispersity in ethanol. The anatase lattice showed disorder and had oxygen vacancies. From the XPS analysis, the existence of 14% of Ti 3+ was established. The functionalized sample remained thermally stable up to 250 °C, beyond which it transformed into a graphite-titania nanocomposite. The interfacial ligand (ester) to metal (Ti) charge transfer (LMCT) transitions were present in the UV-visible spectrum of the sample and indicated the functionalization to be covalent. Unsaturated OH-groups on the surface yielded a ζ-potential value of -39.8 mV. The covalently functionalized nanotitania was exploited in the adsorptive desulfurization of thiophene, an aromatic sulfur model compound. The consequences of surface adsorption of thiophene were analyzed with the help of UV-visible, FTIR, and 1 H and 13 C NMR spectra and EDS and XPS measurements. The adsorption data, derived from the batch process, were fitted successfully to pseudo-second-order kinetics and the Temkin model. The adsorption capacity of covalently functionalized titania was compared with several other high surface area adsorbents containing thiophilic metal ions.

Nanostructured polymeric materials, functionalized with an appropriate receptor, have opened up newer possibilities for designing a reagent that shows analyte-specific recognition and efficient scavenging of an analyte that has either a detrimental influence on human physiology and environment or on its recovery for further value addition. Higher active surface area, morphological diversity, synthetic tunability for desired surface functionalization, and the ease of regeneration of a nanostructured material for further use have provided such materials with a distinct edge over conventional reagents. The use of a biodegradable polymeric backbone has an added significance owing to the recent concern over the impact of polymers on the environment. Functionalization of biodegradable sodium alginate with AENA (6.85% grafting) as the receptor functionality led to a unique open framework nanoring (NNRG) morphology with a favorable spatial orientation for specific recognition and efficient binding to uranyl ions (U) in an aqueous medium over a varied pH range. Nanoring morphology was confirmed by transmission electron microscopy and atomic force microscopy images. The nanoscale design maximizes the surface area for the molecular scavenger. A combination of all these features along with the reversible binding phenomenon has made NNRG a superior reagent for specific, efficient uptake of UO 2 2+ species from an acidic (pH 3-4) solution and compares better than all existing UO 2 2+ -scavengers reported till date. This could be utilized for the recovery of uranyl species from a synthetic acidic effluent of the nuclear power. The results of the U uptake experiments reveal a maximum adsorption capacity of 268 mg of U per g of NNRG in a synthetic nuclear effluent. X-ray photoelectron spectroscopy studies revealed a reductive complexation process and stabilization of U(IV)-species in adsorbed uranium species (U@NNRG).

In the present investigation, chitosan (CH) was supramolecularly cross-linked with thiobarbituric acid to form CT. CT was well characterized by UV, scanning electron microscopy-energy-dispersive X-ray analysis, Fourier transform infrared, NMR, differential scanning calorimetry, thermogravimetric analysis, and X-ray diffraction analyses, and its adsorption potential for elemental mercury (Hg 0 ), inorganic mercury (Hg 2+ ), and methyl mercury (CH 3 Hg + ) was investigated. Adsorption experiments were conducted to optimize the parameters for removal of the mercury species under study, and the data were analyzed using Langmuir, Freundlich, and Temkin adsorption isotherm models. CT was found to have high adsorption capacities of 1357.69, 2504.86, and 2475.38 mg/g for Hg 0 , Hg 2+ , and CH 3 Hg + , respectively. The adsorbent CT could be reused up to three cycles by eluting elemental mercury using 0.01 N thiourea, inorganic mercury using 0.01 N perchloric acid, and methyl mercury with 0.2 N NaCl., Competing Interests: The authors declare no competing financial interest.

A unique fluorescence resonance energy transfer (FRET) process is found to be operational in a unilamellar lipid self-assembly in the aqueous phase. A newly synthesized naphthyl based long chain lipid derivative [N-(naphthalene-1-ylmethyl)tetradecane-1-ammonium chloride, 14NA + ] forms various self-assembled architectures in the aqueous phase. Controlled changes in lipid concentration lead to a transition of the self-assemblies from micelles to vesicles to rods. In the presence of cucurbit[7]uril (CB7), 14NA + forms a host-guest [2]pseudorotaxane complex (CB7∋14NA + ) and secondary interactions lead to the formation of a lipid bilayer with hydrophobic pockets situated in between the layers. The change in the structure of 14NA + assemblies, interaction with CB7 and formation of supramolecular assemblies of CB7∋14NA + were examined using light scattering, spectroscopic, and microscopic techniques. Entrapment of a luminescent dye, anthracene within the hydrophobic bilayer of the supramolecular assembly CB7∋14NA + favors a modified luminescent response due to an efficient FRET process. Further, the FRET process could be controlled by thermal and chemical stimuli that induce transformation of unilamellar vesicles.

Reagents that allows detection and monitoring of crucial biomarkers with luminescence ON response have significance in clinical diagnostics. A new coumarin derivative is reported here, which could be used for specific and efficient chemodosimetric detection of cysteine, an important biomarker. The probe is successfully used for studying the biochemical transformation of N-acetylcysteine, a commonly prescribed Cys supplement drug to Cys by aminoacylase-1 (ACY-1), an important and endogenous mammalian enzyme. The possibility of using this reagent for quantification of ACY-1 in blood serum samples is also explored. Nontoxic nature and cell membrane permeability are key features of this probe and are ideally suited for imaging intracellular Cys in normal and cancerous cell lines. Our studies have also revealed that this reagent could be utilized as a redox switch to monitor the hydrogen-peroxide-induced oxidative stress in living SW480 cell lines. Peroxide-mediated cysteine oxidation has a special significance for understanding the cellular-signaling events.

Palm shell-based adsorbents prepared under five different thermochemical conditions and palm shell powder have been shown to be quite effective for removal of uranium from aqueous solutions. X-ray photoelectron spectroscopy (XPS), extended X-ray absorption fine structure (EXAFS), and Fourier transform infrared spectroscopy (FTIR) have been used to determine information about the speciation and binding of uranium on the adsorbents under study. Studies indicate that the uranium which is present as uranyl ion in aqueous solution is present in mixed valence states (U(IV), U(V), and U(VI)) when it is bound to the adsorbents. The mechanism of adsorption is likely to be adsorption-coupled reduction as well as complexation. Adsorption of uranium, cesium, and iron was found to be quantitative in binary as well as ternary mixtures.

A novel fluorescent complex {(UO(2))(2)(CB5)}(NO(3))(4)·4HNO(3).3H(2)O (U2CB5) is obtained from cucurbit[5]uril (CB5) and uranyl nitrate under ambient temperature conditions. The crystal structure revealed that two uranyl ions are coordinated to the two open portals of CB5 giving a closed molecular capsule, which further connected through CB5 molecules to give two-dimensional frameworks. The U2CB5 complex was further investigated by NMR, FTIR and TGA techniques. The Fluorescence of uranyl ion was found to be enhanced due to complexation with cucurbituril.