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Soil conditioning optimization of sandy pebble soil with different fine contents and prediction by machine learning
Negatively charged α-synuclein condensate modulates partitioning of molecules
Amplifying Circularly Polarized Luminescence with High Dissymmetry Factor over 10 <sup>−2</sup> Based on Robust Point Chirality Triptycene Derivatives
Abstract Chiral organic luminescent materials are promising candidates as direct emitting layers (EMLs) in circularly polarized organic light‐emitting diodes (CP‐OLEDs). However, most conventional systems suffered poor thermal stability of chiral configurations and low luminescent dissymmetry factors. Herein, we reported a pair of triptycene‐bridged enantiomers with a point chirality and a donor–acceptor architecture. Robust point chirality, originating from quaternary bridgehead‐carbons, prevented the common racemization during thermal sublimation. Thanks to the reduced electric transition dipole moment (µ e ) in donor–acceptor architecture, tuned parallel alignment between the further reduced µ e and magnetic transition dipole moment (µ m ) in the exciplex emitter, and the utilized chiral exciplex host for energy transfer to phosphor, the corresponding dissymmetry factors of emitters were sequentially amplified from 3.3 × 10 −4 to 4.5 × 10 −3 , and to 8.1 × 10 −3 . Remarkably, the CP‐OLED device simultaneously achieved outstanding electroluminescence performance with a high external quantum efficiency of 31.8% and a large dissymmetry factor of 2.2 × 10 −2 . This work provided a viable pathway for developing high‐performance CP‐OLED materials through synergistic structural, material, and device engineering.
Environmental contaminants drive insecticide resistance in Anopheles mosquitoes in Ghana
Abstract Insecticide-based interventions such as IRS and LLINs have significantly reduced malaria transmission globally. However, their sustainability is increasingly threatened by insecticide resistance. While insecticide and pesticide use are known resistance drivers, the role of environmental contaminants remains underexplored. This study investigated the impact of environmental contaminants on insecticide resistance by sampling Anopheles larvae from six sites in Ghana, including petroleum spill sites, mining areas and industrial zones. WHO bioassays revealed resistance to clothianidin (Mortality rate (MR) = 54% – 80%) and chlorfenapyr (MR = 80% − 84%) in all site categories. Interestingly, high-intensity resistance to pirimiphos methyl (MR = 10x = 1.7%) was detected in vectors from Obuasi. High-intensity pyrethroid resistance [deltamethrin (MR = 10x = 79–92%); permethrin (MR = 10x = 74–95%)] was observed across all sites, with varying frequencies of kdr mutations ( L995F , V402L , I1527T , P1874L ; 0.12–0.98) were observed across all sites. High allele frequency of Ace-1 (0.62) was observed in Obuasi. Chemical analyses of water from breeding habitats revealed significant associations between heavy metals and insecticide resistance ( P = 0.04). Anopheles coluzzii (81.7%) was the dominant species across all sites. These findings provide evidence that environmental contaminants may contribute to insecticide resistance. There is an urgent need for enhanced surveillance and resistance management strategies for effective malaria vector control.
TORC2 and MAPK signaling pathways regulate mitochondrial degradation induced by iron starvation in Schizosaccharomyces pombe
Radical Reactivity of Thioimidates for Diversified Polymeric Amidines with Tunable Properties
Abstract The first reactions of thioimidates under radical‐mediated conditions are described along with the delineation of structural factors that impact radical reactivity and possible side reactions. Thioimidate‐containing copolymers with methylmethacrylate (MMA) are synthesized through radical‐mediated, chain‐growth polymerization. These materials serve as a synthetic branch point for facile conversion into amidines by treatment with a weak acid and an external amine. Our approach allows for more diverse amidine structures than have been previously reported in polymers. This chemistry also enables crosslinking to form novel hydrogels with finely tuned acid–base behavior. Subsequent examination of the acid–base properties revealed that these features are preserved across linear, soluble amidine polymers to cross‐linked amidine gel polymer architectures.
Experimental and numerical study on the effect of web openings on the torsional behavior of pre-compressed hollow UHPC beams
Abstract Hollow ultra-high-performance concrete (UHPC) members subjected to axial pre-compression and torsion represent realistic loading scenarios commonly observed in modern engineering structures, including bridge box girders, prestressed members, and high-rise tubular columns. The inclusion of web openings further reflects practical design requirements. However, the combined effect of pre-compression, torsion, and openings on UHPC members remains insufficiently addressed in literature. To address this gap, the present study integrates experimental work with numerical simulation to provide novel insights into the structural behavior of UHPC beams under complex loading scenarios. The experimental study involves testing five UHPC pre-compressed reinforced hollow beams with central openings under torsion. Their results are presented in terms of cracking and ultimate torque, failure modes, cracking pattern, elastic and cracked torsional stiffness, post-cracking load-carrying capacity, torsional ductility, strain in lower steel bars and torque–angle of twist curve. In the numerical study, 23 UHPC beams (including the 5 tested beams) are modeled using the finite element method with Abaqus software. The presentation of numerical results includes some measurements that could not be experimentally reported. Based on the findings, key recommendations are also proposed to guide future design and implementation of UHPC members under combined loading.
Uncovering mRNA sequences that control translation initiation
Real-time monitoring of secretory protein traffic for investigating trafficking regulators of ACE2 in living cells
Neurons ensheathed by perineuronal nets are prone to hyperphosphorylation of tau protein in the hibernating Syrian hamster brain
Abstract Perineuronal nets (PNNs) are a specialized form of neuronal extracellular matrix that often ensheath highly active cells, such as parvalbumin-positive (PV+) interneurons. Net-bearing neurons have been shown to be devoid of pathological aggregates of hyperphosphorylated tau protein (p-tau), suggesting they may serve neuroprotective functions. P-tau is a major hallmark of tauopathies like Alzheimer’s disease (AD) but is also naturally present in the brains of hibernating mammals during the torpor phase. However, the relationship between PNNs and p-tau in both pathological and physiological contexts remains unclear. In this study, we examined the association between PNNs, PV, and p-tau in the neocortex of hibernating Syrian hamsters. We observed consistent PNN expression across euthermic and torpid states. Unexpectedly, PNN-enwrapped neurons showed a higher prevalence of p-tau (82%) compared to the overall neuronal population (60%) during torpor. Similarly, PV+ interneurons displayed a high prevalence of p-tau (78%). These findings suggest that PNNs do not prevent tau hyperphosphorylation under physiological conditions like hibernation, in contrast to their potential neuroprotective role in AD pathology. Instead, specific neuronal subsets, such as PNN-enwrapped PV+ interneurons, are likely to exhibit p-tau during torpor. Further analysis of the interplay between p-tau, PNNs, and PV+ interneurons may therefore reveal adaptive strategies for neuronal protection and metabolic regulation, with implications for neurodegeneration and brain metabolic stress.
Structure, regulation and assembly of the photosynthetic electron transport chain
Neddylation inhibitor MLN4924 enhances H3K18 lactylation via binding to LDH and downregulates ITGB4 to block metastasis
Retraction Note: Long non-coding RNA MLLT4 antisense RNA 1 induces autophagy to inhibit tumorigenesis of cervical cancer through modulating the myosin-9/ATG14 axis
Functions and therapeutic applications of pseudouridylation
Metabolomics analysis of SNAT2-deficient cells: Implications for the discovery of selective small-molecule inhibitors of an amino acid transporter
Tailoring Tubular Supramolecular Polymers with Polar Lumens to Host Hydrophilic Dye Molecules
Abstract Supramolecular polymers are living an intense research period in which new synthetic strategies, unusual morphologies, and diverse promising applications are being explored. We contribute here to this field with the development of a unique class of supramolecular polymers that are able to selectively encapsulate guest molecules within their lumen. This is achieved through a rational design of the monomer units, which self‐assemble in amphiphilic cyclic entities that then stack into lipophilic tubular architectures that contain a polar pore. These tailored assemblies are able to host hydrophilic dye molecules that are complementary in size and chemical affinity for the pore coating. Dye extraction is characterized by: (1) the emergence of the dye absorption and emission features in solution, (2) a red shift of the absorption and emission maxima, caused by a confined environment of high viscosity, and (3) an energy transfer process from the monomer at the tube's walls to the included dye guest, which was characterized by photoluminescence (PL), excitation, and transient absorption measurements. When different dyes are co‐encapsulated, the tubular supramolecular polymer provides a unidimensional confined chiral environment to promote sequential energy transfer processes between them.
Distinct liver sections exhibit sex-specific gene expression patterns in Lewis rats
Abstract Sex-specific differences in liver gene expression have previously been reported in humans and rodents. Clinically, female-to-male liver transplants are known to be associated with adverse post-transplantation outcomes. However, the underlying molecular mechanisms remain largely unknown. Sex-specific gene expression differences may be involved in the post-transplantation outcomes. Here, we analyse sex-specific differences in liver gene expression of Lewis rats on a genome-wide scale. In total, 543 genes exhibited a differential gene expression between male (n = 4) and female (n = 4) rats, with the largest difference found for the transcript ENSRNOG00000009273.7 (log2FC = 10.69, p < 2.2*10− 308). Genes downregulated (n = 272) in males were enriched for cholesterol homeostasis and late oestrogen response. We further analysed inter- and intra-sex gene expression differences in three individual liver sections to evaluate liver heterogeneity. Although several genes exhibited a sex-specific expression in all three liver sections (n = 240), distinct expression patterns within each individual section were determined. Variations between sections were even evident within the same sex with male liver sections revealing more differentially expressed genes (male n = 40, female n = 11). Consequently, studies investigating liver-specific gene expressions should consider this intrahepatic heterogeneity to avoid introducing potential biases. Subsequent studies ought to explore gene expression differences between the sexes pre- and post-transplantation, particularly regarding a female-to-male transplants.
Proteome solubility is differentially reshaped by thermal stress and regulators of ubiquitination
Surface Protected Organozirconium Catalyzes C─H Alumination of Saturated Hydrocarbons
Abstract Surface grafted organozirconium catalyzes C─H/Et─Al exchange reactions, involving saturated hydrocarbons and AlEt 3 , to afford organoaluminum compounds and ethane. The Zr(O t Bu) 3 @SiO 2 ‐Al 2 O 3–700 ( 1 ) catalyst contains monopodal ≡SiO─Zr(O t Bu) 3 and only a few residual silanols (<5%). Nonetheless, these silanols are the Achille's heel of 1 , providing a pathway for surface and catalyst degradation during catalysis, limiting the alkylaluminum yield and catalyst turnover. Support degradation, involving the cleavage of Si─O bonds by activated surface organometallics, is inhibited by capping silanols with ─SiMe 3 . Residual silanols in 1 react with allyltrimethylsilane, as determined by solid‐state 13 C and 29 Si nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and reaction stoichiometry, to form Zr(O t Bu) 3 /SiMe 3 @SiO 2 ‐Al 2 O 3–700 ( 2 ), which is resistant to degradation by AlEt 3 . C─H alumination of dodecane catalyzed by 2 produces higher yields of the 1‐dodecylaluminum product in comparison to 1 , and in >95% selectivity. Additionally, methane undergoes 2 ‐catalyzed C─H alumination, providing a route to AlMe 3 .