Transport Pathways Research Articles

Half-Covered ‘Glitter-Cake’ AM@SE Composite: A Novel Electrode Design for High Energy Density All-Solid-State Batteries

All-solid-state batteries (ASSBs) are pursued due to their potential for better safety and high energy density. However, the energy density of the cathode for ASSBs does not seem to be satisfactory due to the low utilization of active materials (AMs) at high loading. With small amount of solid electrolyte (SE) powder in the cathode, poor electrochemical performance is often observed due to contact loss and non-homogeneous distribution of AMs and SEs, leading to high tortuosity and limitation of lithium and electron transport pathways. Here, we propose a novel cathode design that can achieve high volumetric energy density of 1258 Wh L-1 at high AM content of 85 wt% by synergizing the merits of AM@SE core-shell composite particles with conformally coated thin SE shell prepared from mechanofusion process and small SE particles. The core-shell structure with an intimate and thin SE shell guarantees high ionic conduction pathway while unharming the electronic conduction. In addition, small SE particles play the role of a filler that reduces the packing porosity in the cathode composite electrode as well as between the cathode and the SE separator layer. The systematic demonstration of the optimization process may provide understanding and guidance on the design of electrodes for ASSBs with high electrode density, capacity, and ultimately energy density.

Highly Permselective Contorted Polyamide Desalination Membranes with Enhanced Free Volume Fabricated by mLbL Assembly.

The permeability-selectivity trade-off in polymeric desalination membranes limits the efficiency and increases the costs of reverse osmosis and nanofiltration systems. Ultrathin contorted polyamide films with enhanced free volume demonstrate an impressive 8-fold increase in water permeance while maintaining equivalent salt rejection compared to conventional polyamide membranes made with m-phenylenediamine and trimesoyl chloride monomers. The solution-based molecular layer-by-layer (mLbL) deposition technique employed for membrane fabrication sequentially reacts a shape-persistent contorted diamine monomer with a trimesoyl chloride monomer, forming highly cross-linked, dense polyamide networks while avoiding the kinetic and mass transfer limitations of traditional interfacial polymerization. The mLbL process allows precise nanoscale control over polyamide selective layer thickness, network structure, and surface roughness. The resulting controlled film thicknesses enable direct measurements of water and NaCl permeabilities. The permselectivities of contorted polyamide membranes surpass those of commercial desalination membranes and approach the reported polyamide upper bound. Solution-diffusion transport modeling indicates that this high permselectivity may be attributed to enhanced water transport pathways in the contorted polyamides that increase water diffusivity-permeability while maintaining high solute rejection through solubility-selectivity.

Dissolved phosphorous through dry-wet-dry transitions in a small-dammed river basin: integrated understanding on transport patterns, export controls, and fate.

An integrated understanding of dissolved phosphorous (DP) export mechanism and controls on export over dry and wet periods is crucial for riverine ecological restorations in dammed river basins considering its high bioavailability and retention rates at dams. Riverine DP transport patterns (composition, sources, and transport pathways), export controls, and fate were investigated over the 2020 wet season (5 events) and dry seasons before and after it (2 events: dry(before) and dry(after)) in a semi-arid, small-dammed watershed to comprehend the links between terrestrial DP sources and aquatic DP sinks. Close spatiotemporal monitoring of the full range of phosphorous and total suspended solids (TSSs) and subsequent analyses (hysteresis, hierarchical partitioning, and coefficient of variation) provided the basis for the study. Total-DP (TDP) shared 13-39% (25%) of total-P (TP) through storms, dissolved organic-P (DOP) shared 6-21% (12%), and phosphate-P shared (PO4-P) 7-22% (13%). DP forms displayed strong connections with discharge trends across the wet season, and marked changes in the shares were reported over dry-wet and wet-dry transitions. The DOP fraction of TDP increased from 4% in dry(before) baseflow to 64% at the end of the wet season. The DOP flux increment in stormflow was 20 folds compared to dry(before) baseflow, while that of PO4-P was 2 folds. DOP displayed the least spatial source heterogeneity with minimum anthropogenic pressure on inherent fluxes. DOP originated from overland and near-stream soil sources and was transported via surface runoff and soil water runoff, respectively. Across the wet season, the attrition of overland DOP sources and activation of near-stream soil DOP sources through strengthened hydrological connectivity governed the seasonal DOP trends. Surface and groundwater runoff pathways were important for PO4-P delivery during stormflow; nonetheless, wastewater treatment plant (WWTP) effluent was the main PO4-P source under both baseflow and stormflow regimes, followed by near-stream traditional agriculture lands. The interaction patterns of small dam systems with DP inputs through dry-wet periods were explained. The riverine PO4-P fluxes were profoundly impacted by in-stream biogeochemical and physical processes and small dam systems, while riverine DOP fluxes were relatively less influenced.

The Design of Intrinsically Conductive Metal‐Organic Frameworks for Thermoelectric Materials

Thermoelectric (TE) materials offer exciting promise in the development of sustainable, green energy alternatives. Ideal TE materials promote high electrical conductivity, whilst effectively scattering phonons for reduced thermal conductivity, thus giving the phonon‐glass electron‐crystal concept. Metal‐organic frameworks (MOFs) have emerged as a versatile class of materials that could meet these criteria. The high crystallinity of MOFs can offer effective pathways for charge transport whilst their intrinsic high porosity yields ultralow thermal conductivity. The high structural diversity of MOFs, owing to the versatile coordination of metal cation/cluster and linker offers the potential to systematically tune their properties for TE performance. This review examines the advancement in the design strategies that have thus far been implemented toward intrinsically conductive MOFs and how these should be tailored for application toward TE materials. By addressing the challenges and leveraging the unique properties of MOFs, future research can pave the way for innovative and efficient TE MOF materials.

Effects of Enterocytozoon hepatopenaei infection on intestinal immune defense and physiological processes of Penaeus vannamei

As the main pathogen causing growth retardation, EHP is considered to be mainly parasitic in the hepatopancreas of shrimp. However, the intestines of shrimp infected with EHP frequently exhibit syndromes such as jejunum and white midgut. Therefore, the challenge experiment was carried out in this study to compare the differences in intestinal histology, digestion and absorption, immune defense and oxidative stress of P. vannamei between the control group and EHP infection group. Histological analysis showed that EHP infection significantly damaged the intestine of the shrimp, including intestinal villus rupture and outer membrane impairment. Concurrently, EHP infection can trigger intestinal immune response, and the expression of key immune genes like Toll, myeloid differentiation factor, anti-lipopolysaccharide factor, and Relish was significantly enhanced, while the expression of IMD and alkaline phosphatase was suppressed. Additionally, antioxidant genes manganese superoxide dismutase, catalase, glutathione peroxidase, glutathione-S-transferase, and nuclear factor E2-related factor 2 were up-regulated to varying extents in EHP infection group, and the contents of lipid peroxides and malondialdehyde were heavily accumulated. Moreover, the expression levels of key genes involved in nutrient absorption, transport and synthesis, such as glucose transporter 1, Na+-K+ATPase, fatty acid synthase, acetyl-CoA carboxylase, rapamycin kinase, mTOR regulation-related protein, eukaryotic translation initiation factor 4E binding protein, ribosomal protein S6 kinase, were significantly up-regulated. However, the activities of amylase, lipase, and trypsin were inhibited in EHP infection group throughout the experiment. In summary, EHP infection damaged the intestine of P. vannamei, accompanied by immune response and oxidative stress. At the same time, nutrient transport and synthesis pathways were activated, while digestive enzyme activities were inhibited, indicating that in order to maintain survival, shrimps must accelerate material transport. Unfortunately, it remains in a state of nutrient deficiency that ultimately affects growth.

The metabolite transporters of C4 photosynthesis.

C4 photosynthesis is a highly efficient form of photosynthesis that utilises a biochemical pump to concentrate CO2 around rubisco. Although variation in the implementation of this biochemical pump exists between species, each variant of the C4 pathway is critically dependent on metabolite transport between organelles and between cells. Here we review our understanding of metabolite transport in C4 photosynthesis. We discuss how the majority of our knowledge of the metabolite transporters co-opted for use in C4 photosynthesis has been obtained from studying C3 plants, and how there is a pressing need for in planta validation of transporter function in C4 species. We further explore the diversity of transport pathways present in disparate C4 lineages and highlight the important gaps in our understanding of metabolite transport in C4 plants. Finally, through integration of functional and transcriptional data from multiple C3 and C4 plants we propose a molecular blueprint for metabolite transport for NAD-ME photosynthesis.

In Situ Copolymerizing ZrO2 with Hydrogel Electrolytes toward High‐Rate and Long‐Life Quasi‐Solid‐State Zn–Ion Batteries

AbstractHydrogel is adopted as a promising alternative electrolyte for the zinc–ion batteries (ZIBs) due to its water‐retaining capacity and high ionic conductivities. However, the high content of free water molecules will affect the operation of electrolytes in ZIBs, resulting in the uncontrolled growth of zinc dendrites and related side reactions. Herein, a functional hydrogel electrolyte is developed by in situ copolymerizing the ceramic ZrO2 with acrylamide and 2‐Acrylamido‐2‐methylpropane sulfonic acid to adjust the ion transport behavior, further improve zinc ions' depositional behavior. The interaction between ZrO2 and ─SO3H groups within the hydrogel is capable of inducing the free migration of zinc ions, resulting in a novel transport pathway, thereby enhancing the diffusion rate of zinc ions with an ionic conductivity of 38.3 mS cm−1. The hydrogen bonding between ceramic particles and free water molecules of the hydrogel electrolyte enables it to achieve stable operation under large current densities (8 mA cm−2, 4 mAh cm−2). Moreover, a full battery with polyaniline (PANI@ZrO2) displays excellent stability (1500 cycles) with a capacity retention rate of 79.2%. The proposed work provides an insightful design of high‐performance electrolyte materials for energy storage by manipulating the zinc behavior.

Structural Control of Photoconductivity in a Flexible Titanium-Organic Framework.

The soft nature of Metal-Organic Frameworks (MOFs) sets them apart from other non-synthetic porous materials. Their flexibility allows the framework components to rearrange in response to environmental changes, leading to different states and properties. The work extends this concept to titanium frameworks, demonstrating control over charge transport in porous molecular crystals. MUV-35 is a two-fold catenated framework composed of heterometallic TiMn2 trimers and electron donor 4,4',4″-(benzo[1,2-b:3,4-b':5,6-b″]trithiophene-2,5,8-triyl)tribenzoic acid (H3BTTTB) linkers, forming a rare sit-c net topology that can fold to reduce its volume by ≈40% through a single-crystal transformation controlled by linker conformation in open, intermediate, and closed states. This process, driven by a free energy difference of ≈300kJmol-1, originates from the formation of a continuous network of non-covalent interactions that force the spontaneous loss of the solvent in the pores of the framework to establish charge transport pathways that afford photocurrents of 2.5 × 10-3Sm-1 under visible light for an ON/OFF ratio (∆R) of four orders of magnitude. This photoconductivity rivals the best conductivity values described for though-transport conductive MOFs while maintaining a porosity of ≈1.000m2g-1.

Enhanced Charge Transport through Ion Networks in Highly Concentrated LiSCN‐Polyethylene Carbonate Solid Polymer Electrolytes

Challenging the preference for bulky anions due to low binding energy with Li+ ion, the lithium thiocyanate‐polyethylene carbonate (LiSCN‐PEC) solid polymer electrolyte (SPE) demonstrates higher ionic conductivities (3.16 × 10−5 S cm−1) at polymer‐in‐salt concentration (100 mol%) compared to those with lithium bis(fluorosulfonyl)imide (LiFSI, 1.01 × 10−5 S cm−1) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI, 1.72 × 10−7 S cm−1). Through the careful selection of PEC and LiSCN as components of SPE, the carbonyl stretching of PEC and the SCN− stretching band as vibrational reporters provide detailed structural insights into the Li+ ion transport channel. Spectroscopic investigations reveal that enhanced ion aggregation alters the solvation structure around the Li+ and diminishes the interaction between Li+ and polymer (PEC) with increasing LiSCN concentrations, promoting faster segmental motion as a major transport mechanism. However, the transition observed from subionic to superionic behavior in the Walden plot indicates the onset of segmental motion decoupled charge transport pathway. The SCN− vibrational spectrum elucidates the evolution from a Li–SCN–Li type chain‐like structure to a Li2 > SCN < Li2 type extended ion network with increasing LiSCN concentration, revealing that the ion network provides an alternative channel for Li+ ion transfer at higher concentrations, enhancing conductivity.

Cellular uptake and transport mechanism of lycopene-loaded nanomicelles formed by amphiphilic peptide self-assembly in the intestinal epithelium.

This study aimed to elucidate the transport mechanism of lycopene-loaded nanomicelles to improve intestinal absorption of lycopene. The interactive mechanism between lycopene and nanomicelles was investigated through isothermal titration calorimetry (ITC). The cytotoxicity, cellular uptake, endocytosis, and intracellular transport pathways of lycopene-loaded nanomicelles were investigated using the Caco-2 cell model. The ITC results demonstrated that nanomicelles/lycopene binding was an entropy-driven spontaneous exothermic reaction, and hydrophobic interactions were the main driving force. Lycopene-loaded nanomicelles were not cytotoxic, and uptake of lycopene by Caco-2 cells increased 2.20-fold after nanoencapsulation. The results of intracellular transport of lycopene-loaded nanomicelles indicated that the endoplasmic reticulum, Golgi apparatus, and lysosomes play key roles in this process. The intracellular transport results showed that the endoplasmic reticulum, Golgi apparatus, and lysosomes were important organelles for intracellular transport of lycopene-loaded nanomicelles. Nanomicelles effectively enhance the cellular uptake of lycopene and are promising carriers for its delivery. This study contributes to the understanding of the transport mechanism of nanomicelles through intestinal epithelial cells. © 2025 Society of Chemical Industry.

Strategies for the Viral Exploitation of Nuclear Pore Transport Pathways

Viruses frequently exploit the host’s nucleocytoplasmic trafficking machinery to facilitate their replication and evade immune defenses. By encoding specialized proteins and other components, they strategically target host nuclear transport receptors (NTRs) and nucleoporins within the spiderweb-like inner channel of the nuclear pore complex (NPC), enabling efficient access to the host nucleus. This review explores the intricate mechanisms governing the nuclear import and export of viral components, with a focus on the interplay between viral factors and host determinants that are essential for these processes. Given the pivotal role of nucleocytoplasmic shuttling in the viral life cycle, we also examine therapeutic strategies aimed at disrupting the host’s nuclear transport pathways. This includes evaluating the efficacy of pharmacological inhibitors in impairing viral replication and assessing their potential as antiviral treatments. Furthermore, we emphasize the need for continued research to develop targeted therapies that leverage vulnerabilities in nucleocytoplasmic trafficking. Emerging high-resolution techniques, such as advanced imaging and computational modeling, are transforming our understanding of the dynamic interactions between viruses and the NPC. These cutting-edge tools are driving progress in identifying novel therapeutic opportunities and uncovering deeper insights into viral pathogenesis. This review highlights the importance of these advancements in paving the way for innovative antiviral strategies.

Gradient Design with Low-tortuosity Overcoming Kinetic Limitations in High-Loading Solid-State Cathodes.

The extensive commercialization of practical solid-state batteries (SSBs) necessitates the development of high-loading solid-state cathodes with fast charging capability. However, electrochemical kinetics are severely delayed in thick cathodes due to tortuous ion transport pathways and slow solid-solid ion diffusion, which limit the achievable capacity of SSBs at high current densities. In this work, we propose a conductivity gradient cathode with low-tortuosity to enable facile ion transport and counterbalance ion concentration gradient, thereby overcoming the kinetic limitations and achieving fast charging capabilities in thick cathodes. The LiNi0.8Co0.1Mn0.1O2 cathodes deliver a room-temperature (RT) capacities of 147 and 110 mAh g-1 at 5 C and 10 C, respectively, and meanwhile achieve a RT areal capacity of 3.3 mAh cm-² at 3 C, enabling SSBs simultaneously high energy and power densities. The universality of this strategy is demonstrated in LiFePO4 cathodes, providing a novel solution for fast charging and large-scale application of high-loading SSBs.

Aerosols in the Mixed Layer and Mid-Troposphere from Long-Term Data of the Italian Automated Lidar-Ceilometer Network (ALICENET) and Comparison with the ERA5 and CAMS Models

Aerosol vertical stratification significantly influences the Earth’s radiative balance and particulate-matter-related air quality. Continuous vertically resolved observations remain scarce compared to surface-level and column-integrated measurements. This work presents and makes available a novel, long-term (2016–2022) aerosol dataset derived from continuous (24/7) vertical profile observations from three selected stations (Aosta, Rome, Messina) of the Italian Automated Lidar-Ceilometer (ALC) Network (ALICENET). Using original retrieval methodologies, we derive over 600,000 quality-assured profiles of aerosol properties at the 15 min temporal and 15 metre vertical resolutions. These properties include the particulate matter mass concentration (PM), aerosol extinction and optical depth (AOD), i.e., air quality legislated quantities or essential climate variables. Through original ALICENET algorithms, we also derive long-term aerosol vertical layering data, including the mixed aerosol layer (MAL) and elevated aerosol layers (EALs) heights. Based on this new dataset, we obtain an unprecedented, fine spatiotemporal characterisation of the aerosol vertical distributions in Italy across different geographical settings (Alpine, urban, and coastal) and temporal scales (from sub-hourly to seasonal). Our analysis reveals distinct aerosol daily and annual cycles within the mixed layer and above, reflecting the interplay between site-specific environmental conditions and atmospheric circulations in the Mediterranean region. In the lower troposphere, mixing processes efficiently dilute particles in the major urban area of Rome, while mesoscale circulations act either as removal mechanisms (reducing the PM by up to 35% in Rome) or transport pathways (increasing the loads by up to 50% in Aosta). The MAL exhibits pronounced diurnal variability, reaching maximum (summer) heights of > 2 km in Rome, while remaining below 1.4 km and 1 km in the Alpine and coastal sites, respectively. The vertical build-up of the AOD shows marked latitudinal and seasonal variability, with 80% (30%) of the total AOD residing in the first 500 m in Aosta-winter (Messina-summer). The seasonal frequency of the EALs reached 40% of the time (Messina-summer), mainly in the 1.5–4.0 km altitude range. An average (wet) PM > 40 μg m−3 is associated with the EALs over Rome and Messina. Notably, 10–40% of the EAL-affected days were also associated with increased PM within the MAL, suggesting the entrainment of the EALs in the mixing layer and thus their impact on the surface air quality. We also integrated ALC observations with relevant, state-of-the-art model reanalysis datasets (ERA5 and CAMS) to support our understanding of the aerosol patterns, related sources, and transport dynamics. This further allowed measurement vs. model intercomparisons and relevant examination of discrepancies. A good agreement (within 10–35%) was found between the ALICENET MAL and the ERA5 boundary layer height. The CAMS PM10 values at the surface level well matched relevant in situ observations, while a statistically significant negative bias of 5–15 μg m−3 in the first 2–3 km altitude was found with respect to the ALC PM profiles across all the sites and seasons.

Transcriptome Analysis Reveals the Key Genes and Pathways for Growth, Ion Transport, and Oxidative Stress in Post-Larval Black Tiger Shrimp (Penaeus monodon) Under Acute Low Salt Stress.

As an abiotic stress factor, salinity significantly affects the physiological activities of crustaceans. In this study, transcriptome sequencing was used to evaluate the mechanism of ion transport and the physiological response of black tiger shrimp (Penaeus monodon) under low salt stress. Four hundred post larval (PL) stage P. monodon were distributed in eight experimental tanks and exposed to 3 or 5 ppt salt concentrations for 96h. Low salinity significantly reduced the survival rate of shrimp but simultaneously activated the activity of ion transporter enzymes Na+/K+-ATPase (NKA) and Ca2+/Mg2+-ATPase), the expression of NKA, galectin 10, and cytochrompe c peroxidase genes, and the activity and expression of antioxidant-related genes (superoxide dismutase, catalase, heat shock protein 60). Low salt stress activated the urea cycle but significantly inhibited glutathione metabolization-related indicators (glutamate dehydrogenase, glutaminase, glutamic acid). RNA-seq analysis identified 221 differentially expressed genes (78 up-regulated and 143 down-regulated). Quantitative real-time PCR and RNA-seq results of 11 of them were consistent, illustrating the validity of the transcriptomic predictions. Gene set enrichment analysis results showed that calcium ion transmembrane transport, calmodulin binding, the stress-activated protein kinase signaling cascade, and regulation of the cytosolic calcium ion concentration process were significantly enriched. These results showed that low salt stress activated the calcium-dominated ion transport pathway and promoted molting growth of P. monodon. They also indicate that there is potential for larval rearing shrimp under low salt conditions.

Mass Spectrometry-Based Spatial Multiomics Revealed Bioaccumulation Preference and Region-Specific Responses of PFOS in Mice Cardiac Tissue.

The distribution and bioaccumulation of environmental pollutants are essential to understanding their toxicological mechanism. However, achieving spatial resolution at the subtissue level is still challenging. Perfluorooctanesulfonate (PFOS) is a persistent environmental pollutant with widespread occurrence. The bioaccumulation behavior of PFOS is complicated by its dual affinity for phospholipids and protein albumin. It is intriguing to visualize the distribution preference of PFOS and investigate the differential microenvironment responses at a subtissue level. Herein, we developed a mass-spectrometry (MS)-based spatial multiomics workflow, integrating matrix-assisted laser desorption/ionization MS imaging, laser microdissection, and liquid chromatography MS analysis. This integrated workflow elucidates the spatial distribution of PFOS in mouse cardiac tissue, highlighting its preferential accumulation in the pericardium over the myocardium. This distribution pattern results in greater toxicity to the pericardium, significantly altering cardiolipin levels and disrupting energy metabolism and lipid transport pathways. Our integrated approach provides novel insights into the bioaccumulation behavior of PFOS and demonstrates significant potential for revealing complex molecular mechanisms underlying the health impacts of environmental pollutants.

Complementary Strategies to Identify Differentially Expressed Genes in the Choroid Plexus of Patients with Progressive Multiple Sclerosis.

Multiple sclerosis (MS) is a neurological disease causing myelin and axon damage through inflammatory and autoimmune processes. Despite affecting millions worldwide, understanding its genetic pathways remains limited. The choroid plexus (ChP) has been studied in neurodegenerative processes and diseases like MS due to its dysregulation, yet its role in MS pathophysiology remains unclear. Our work re-evaluates the ChP transcriptome in progressive MS patients and compares gene expression profiles using diverse methodological strategies. Samples from patient and healthy control RNASeq sequencing of brain tissue from post-mortem patients (GEO: GSE137619) were used. After an evaluation and quality control of these data, they had their transcripts mapped and quantified against the reference transcriptome GRCh38/hg38 of Homo sapiens using three strategies to identify differentially expressed genes in progressive MS patients. Functional analysis of genes revealed their involvement in immune processes, cell adhesion and migration, hormonal actions, amino acid transport, chemokines, metals, and signaling pathways. Our findings can offer valuable insights for progressive MS therapies, suggesting specific genes influence immune cell recruitment and potential ChP microenvironment changes. Combining complementary approaches maximizes literature coverage, facilitating a deeper understanding of the biological context in progressive MS.

Structural mechanism underlying PHO1;H1-mediated phosphate transport in Arabidopsis.

Arabidopsis PHOSPHATE 1 (AtPHO1) and its closest homologue AtPHO1;H1 are phosphate transporters that load phosphate into the xylem vessel for root-to-shoot translocation. AtPHO1 and AtPHO1;H1 are prototypical members of the unique SPX-EXS family, whose structural and molecular mechanisms remain elusive. In this study, we determined the cryogenic electron microscopy structure of AtPHO1;H1 binding with inorganic phosphate (Pi) and inositol hexakisphosphate in a closed conformation. Further molecular dynamic simulation and AlphaFold prediction support an open conformation. AtPHO1;H1 forms a domain-swapped homodimer that involves both the transmembrane ERD1/XPR1/SYG1 (EXS) domain and the cytoplasmic SYG1/Pho81/XPR1 (SPX) domain. The EXS domain presented by the SPX-EXS family represents a novel protein fold, and an independent substrate transport pathway and substrate-binding site are present in each EXS domain. Two gating residues, Trp719 and Tyr610, are identified above the substrate-binding site to control opening and closing of the pathway. The SPX domain features positively charged patches and/or residues at the dimer interface to accommodate inositol hexakisphosphate molecules, whose binding mediates dimerization and enhances AtPHO1;H1 activity. In addition, a C-terminal tail is required for AtPHO1;H1 activity. On the basis of structural and functional analysis, a working model for Pi efflux mediated by AtPHO1;H1 and its homologues was postulated, suggesting a channel-like mechanism. This study not only reveals the molecular and regulatory mechanism underlying Pi transport mediated by the unique SPX-EXS family, but also provides potential for crop engineering to enhance phosphorus-use efficiency in sustainable agriculture.

Advances in auxin synthesis, transport, and signaling in rice: implications for stress resilience and crop improvement

Auxin, a crucial plant hormone, plays a pivotal role in regulating various aspects of rice growth and development, including cell elongation, root formation, and responses to environmental stimuli. Recent breakthroughs in auxin research have revealed novel regulatory mechanisms, such as the identification of auxin-related genes like DNR1 and OsARF18, which enhance rice nitrogen use efficience and resistance to glufosinate. Additionally, advancements in understanding auxin transport and signaling pathways have highlighted their potential in optimizing tillering, root architecture, and grain yield. This review examines these molecular mechanisms and their interactions with other hormones, emphasizing their integration into breeding programs for improved rice productivity. By synthesizing these findings, we provide a comprehensive overview of how auxin research informs strategies for developing rice varieties with enhanced adaptability and optimized growth, contributing to food security and sustainable agriculture.

Tetrahedral Framework Nucleic Acids as an Efficient Nasal‐to‐Brain Delivery Carrier via Neural Transport Pathways

Tetrahedral Framework Nucleic Acids as an Efficient Nasal‐to‐Brain Delivery Carrier via Neural Transport Pathways

Stable Electrochemical Lithium Extraction Using LiMn2O4 Coated With Lithiated Nafion.

Electrochemical lithium extraction from salt lakes using LiMn2O4 (LMO) presents an eco-friendly, highly controllable, and efficient method. However, its practical application is limited due to its structure instability and manganese dissolution in water. Herein, a high-performance LMO coated with ≈3.5nm thickness lithiated Nafion (Li-Nafion) for electrochemical lithium extraction is reported. The Li-Nafion coating constructs a fast lithium-ion transport pathway and enhances the hydrophilicity of the LMO particles, promoting charge transfer and improving rate capability. Thereby, an enhanced lithium extraction capacity of 4mmolg-1 is achieved. Importantly, the coating significantly inhibits Mn loss in LMO, resulting in significantly improved cyclic stability, with a capacity retention rate of 96% after 50 cycles. Furthermore, the Li-Nafion modified LMO effectively extracts lithium electrochemically in Zabuye salt lake, showcasing practical potential.