Search Results (20,051)

To address the key issues of uneven distribution of functional groups, large dispersion of holographic storage performance across different regions, and poor consistency of storage capacity in traditional PQ/PMMA holographic storage photopolymers, this paper introduces a low-viscosity reactive diluent, tripropylene glycol diacrylate (TPGDA), to modify the matrix. Leveraging the viscosity-reducing and double-bond crosslinking properties of TPGDA, the molecular diffusion behavior of the system was regulated. The effects of TPGDA doping ratio, the ratio of photosensitizer PQ to thermal initiator AIBN, and post-curing process on the holographic performance uniformity of the material were systematically investigated. The uniformity was quantitatively evaluated by the variance of diffraction efficiency at different points. Visible light absorption spectra and Fourier-transform infrared (FT-IR) spectroscopy were employed to reveal the modification mechanism from the perspective of functional group distribution. Actual-data read/write tests were conducted using a collinear holographic storage system. The experimental results show that the optimal TPGDA doping concentration is 40 wt%. For the optimized formulation TPGDA:MMA:AIBN:PQ = 8 g:12 g:0.20 g:0.18 g, the modified material achieves an average diffraction efficiency of 76.58%, and the diffraction efficiency variance decreases from 23.49 (pristine matrix) to 1.64, indicating a significant improvement in performance uniformity. Compared with pure PQ/PMMA, the modified material exhibits an approximately 1.95-fold increase in maximum diffraction efficiency, a 2-fold increase in recording rate, and a 1.6–1.75-fold increase in refractive index modulation. FT-IR spectroscopy confirms that TPGDA optimizes the spatial distribution uniformity of C=C and C=O functional groups. In collinear holographic measurements, the bit error rate (BER) variance of the modified sample is reduced by 40% relative to the pristine matrix, achieving homogeneous storage performance across the entire area while maintaining comparable signal-to-noise ratio (SNR) and BER. Additional short-time UV post-curing can further enhance the diffraction efficiency and refractive index modulation, and a thinner substrate can avoid performance fluctuations caused by incomplete thermal curing of thick samples. This study achieves directional optimization of the holographic uniformity of PQ/PMMA through reactive diluent viscosity reduction modification, providing a new strategy for the formulation design and engineering preparation of high-consistency holographic storage photopolymers. Full article

Background: Psychosocial assessment is a core component of lung transplant candidate evaluation, but total scores and broad candidate categories do not necessarily show how individual psychosocial concerns co-occur or which modifiable domains require further clinical attention. This study describes the development and internal evaluation of a clinical decision-support application that reorganizes Stanford Integrated Psychosocial Assessment for Transplantation (SIPAT) data into structured multidomain profiles. Methods: The application was developed using a retrospective single-center dataset of 496 adult lung transplant candidates. It integrates the SIPAT total score and candidate category with seven SIPAT-derived domain indicators, domain burden scores, cohort-referenced z-scores, graphical displays, and a ranked summary of domains for clinical review. All seven indicator targets were prespecified deterministic functions of SIPAT items or domain scores obtained during the same assessment. Random forest algorithms with sigmoid calibration were used to transform these targets into percentage-scaled display values; they were not trained using independently assessed clinical outcomes. Analyses included descriptive statistics, Spearman correlations, exploratory clustering, resampling-based cluster stability assessment, threshold sensitivity analyses, and subgroup analyses by age, sex, and primary pulmonary diagnosis. Results: Upper display-band classifications were identified for depression-related concerns in 32 candidates (6.5%), anxiety-related concerns in 11 (2.2%), nicotine-related concerns in 56 (11.3%), alcohol-related concerns in 22 (4.4%), illicit drug-use concerns in 11 (2.2%), social-support deficits in 40 (8.1%), and non-adherence-related concerns in 7 (1.4%). Exploratory clustering yielded a low-burden majority group (n = 432), a nicotine-dominant group (n = 53), and a small multidomain-elevation group (n = 11). The generated percentage-scaled indicators were positively associated with their conceptually corresponding SIPAT domains (Spearman’s ρ = 0.321–0.774) and with the total SIPAT score (ρ = 0.406–0.802; all p < 0.001). Sensitivity analyses showed that the smaller clusters were less stable under bootstrap resampling. These findings demonstrate internal alignment with the source instrument but do not constitute validation against independent clinical outcomes. Conclusions: The application provides an early-stage framework for organizing and visualizing SIPAT information and identifying domains that may warrant additional clinical assessment. Its outputs should be interpreted as SIPAT-derived decision-support indicators, not as independently validated probabilities of future clinical events. Prospective studies are required to evaluate usability, clinical impact, and associations with longitudinal outcomes. Full article

Proton exchange membrane fuel cells (PEMFCs) offer high efficiency and zero emissions, but durability remains a major barrier to commercialization. Degradation arises from coupled thermal, mechanical, and chemical stresses, yet these processes are often studied in isolation, reducing the accuracy of lifetime prediction. This paper systematically reviews PEMFC degradation, focusing on the coupling between thermal management failure and hydrogen crossover. Most importantly, it identifies a self-reinforcing thermal–hydrogen feedback in which localized overheating and permeated-hydrogen oxidation mutually amplify membrane defect propagation. Mitigation strategies spanning temperature control, hydrogen crossover suppression, intelligent prediction, and current challenges are then discussed. Mechanistically, thermal mismanagement promotes localized hot spots, while elevated temperature increases hydrogen diffusivity and accelerates defect growth, thereby sharply increasing crossover flux. Permeated hydrogen can be catalytically oxidized near defect sites, releasing additional heat and intensifying local membrane damage. Because the two stressors are coupled rather than independent, single-factor mitigation is insufficient; temperature control and hydrogen crossover suppression must be co-optimized. Future progress requires multiscale frameworks across scales, in situ multiphysics characterization, and artificial intelligence (AI)-driven control, moving from mechanistic understanding to engineering application. Full article

The receptor-binding domain (RBD) of the SARS-CoV-2 Spike protein remains a central target for antiviral drug development. Recent in silico studies have revealed an expansion of amyloidogenic regions within the RBD of the Omicron variant, raising the possibility that amyloid-prone peptide fragments could modulate Spike function or host–virus interactions. In this study, we combined experimental assays with multiscale computational modeling to systematically characterise two short RBD-derived peptides: Pep-2 (YFPLQSYGFQ) from the ancestral Wuhan strain and Pep-3 (YFPLRSYSFR) from the Omicron BA.1 variant, the latter being predicted to have higher amyloidogenic potential. Cell-based assays demonstrated that neither peptide exhibited intrinsic cytotoxic or cytostatic effects on human lung fibroblasts or A549 lung adenocarcinoma cells at physiologically relevant concentrations, whereas significant cytotoxicity was observed in Vero E6 cells. In infection models with the B.1.1.1 (Wuhan) and BA.1 (Omicron) variants, the peptides unexpectedly enhanced virus-induced cytopathic effects at lower concentrations but inhibited viral infection at higher concentrations, indicating to a dose-dependent modulatory role for these short amyloidogenic RBD fragments. Fluorescence spectroscopy measurements did not detect the formation of stable thioflavin-T-positive amyloid fibrils. Computational analyses revealed that both peptides interact with the Spike RBD via multiple energetically favorable yet spatially heterogeneous modes, mostly outside the ACE2-binding site. Moreover, their predicted binding affinities for the ACE2 receptor were comparable, suggesting an additional route of interaction via the host receptor. Collectively, our findings demonstrate that these short amyloidogenic RBD-derived peptides exert a complex antiviral profile, with their interactions with both viral and host factors potentially shaping infection outcomes. This highlights the importance of spatially targeted and conformationally constrained peptide designs to effectively harness amyloidogenic features for antiviral therapy. Full article

Co-fermentation of tea and wine offers a promising route to functional beverages with enhanced sensory complexity and potential health benefits. We co-fermented Marselan (Vitis vinifera L.) grapes with Fu brick tea (0, 0.5, 1.0, 1.5 g/L), a post-fermented tea containing the probiotic fungus Eurotium cristatum. We systematically examined how tea-derived phenolics modulate wine color and aroma. Fu tea addition progressively decreased alcohol (12.24% → 10.86%) and modestly reduced residual sugar, while volatile acidity remained stable, indicating no adverse fermentation impact. HPLC revealed a substantial increase in tea-derived phenolics; chlorogenic acid nearly doubled and became the dominant phenolic compound. CIELab color analysis showed increased lightness (L) and marked decreases in yellow hue (b) and hue angle (h°). Total phenolic content correlated negatively with h° (r = −0.656, p = 0.0205), suggesting that the overall phenolic load—not any single compound—is associated with the shift toward a more stable brick-red hue. PCA showed that chlorogenic acid contributed to both color (PC1) and phenolic (PC2) variation. GC-MS revealed substantial increases in esters and higher alcohols, and the emergence of 1-octen-3-ol, a characteristic metabolite of E. cristatum. C6 compounds associated with herbaceous aromas decreased significantly. Fu tea co-fermentation thus enhanced wine color stability and aroma complexity through a multifaceted phenolic network. Under our conditions, 1.0 g/L Fu tea gave the most favorable balance of color stability and aroma complexity. These findings provide a preliminary theoretical basis for developing tea-wine products, though further mechanistic studies are needed to establish causality. Full article

For sorting mechanisms that operate on a planar platform, the perception module may need to estimate object category, image-plane position, object extent and principal-axis orientation within the computing budget of a low-power device. This paper reports an oriented object detection workflow for a MaixCAM Pro (Shenzhen Sipeed Technology Co., Ltd., Shenzhen, China) waste-sorting prototype. The sensing output is represented by oriented bounding boxes (OBBs), which provide two-dimensional position, rectangular extent and principal-axis orientation for downstream sorting control. To adapt the detector to a small self-built dataset and INT8 deployment, class- and aspect-ratio-aware re-sampling (CAR-RS) repeats selected training images, while class- and aspect-ratio-aware calibration (CAR-Calib) selects a stratified calibration subset for post-training quantization. The YOLO11-OBB model is exported as a static ONNX graph, adapted by exposing the OBB head output tensors, compiled with TPU-MLIR and executed through native MaixPy OBB inference. On the original PC validation split, the baseline and CAR-RS models both obtain 0.995 mAP50, with mAP50–95 values of 0.935 and 0.932, respectively. CAR-RS reduces the angle mean absolute error from 3.403° to 3.201° for objects with aspect ratio greater than or equal to 1.3. On an additional 80-image cross-background test set that was not used for training or calibration, CAR-RS improves precision from 0.839 to 0.907, recall from 0.882 to 0.893 and mAP50 from 0.916 to 0.927, while mAP50–95 changes from 0.797 to 0.789. On a 100-image MaixCAM Pro validation set, the CAR-RS + CAR-Calib INT8 model achieves 0.961 precision, 0.994 recall, 0.977 F1-score and 0.980 mAP50. The deployed INT8 model occupies 11.85 MB and runs at 8.40 FPS. The results support the technical feasibility of executing an OBB detector on MaixCAM Pro, while also showing that independent-scene validation remains necessary for broader deployment. Full article

This study addresses the urgent issue of nitrate-contaminated water by investigating Ni-Pt and Co-Pt catalysts supported on TiO₂, with the aim of improving both photocatalytic efficiency and reaction selectivity. The influence of adding non-noble metal co-catalysts to TiO₂, in addition to Pt, was explored. The synthesized samples were characterized by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), hydrogen temperature-programmed reduction (H₂-TPR), diffuse reflectance UV–Vis spectroscopy, photoluminescence (PL), and X-ray photoelectron spectroscopy (XPS). The assessment of catalytic performance was conducted during the catalytic hydrogenation of nitrate, followed by an evaluation of the photocatalytic performance achieved when the aqueous nitrate solution was irradiated with UV light. The focus is on assessing the synergistic effects of the catalysts supported on TiO₂ in nitrate reduction, as well as their selectivity towards benign reaction products during the photocatalytic process, in contrast to the reactions occurring in the absence of light. Despite the selectivity for nitrite being preserved, the photocatalytic experiments indicated that the selectivity for N₂ reached around 68%, which is about 1.5 times higher than the values observed during the dark catalytic reaction. In contrast, the selectivity for ammonium saw a notable reduction. The findings were discussed in relation to the characteristics of the synthesized materials. Full article

Nano- (NPs, <1 µm) and microplastics (MPs, 1 µm–5 mm) are ubiquitous contaminants whose toxicity to invertebrates carries implications at the individual scale and (although not yet quantitatively validated) at the population scale. This semi-systematic narrative review organizes available evidence within an adverse outcome pathway (AOP) framework, linking primary molecular initiating events (MIEs) to adverse outcomes while flagging evidence strength at each step. It involves a structured synthesis that applies selected PRISMA 2020 transparency principles, namely disclosed databases, a priori eligibility criteria, and explicit harvest and de-duplication counts, but does not attempt the exhaustive paired screening, formal risk-of-bias scoring, or quantitative meta-analysis of a full systematic review; this design was chosen because the marked heterogeneity of particle physicochemistry, exposure regimes, and endpoint metrics across the available literature makes pooled statistical synthesis premature. Evidence is appraised across Daphnia, Artemia, Chironomus, Caenorhabditis elegans, Eisenia, marine mollusks, and crustaceans. Polymer chemistry, size, surface charge, weathering, biofilm formation, additives, and adsorbed co-contaminants shape uptake and downstream toxicity. Reactive oxygen species, mitochondrial dysfunction, lysosomal destabilization, and ER stress recur as coupled key events downstream of four MIEs (direct membrane interaction, protein corona formation, surface-catalyzed redox chemistry, and Trojan horse delivery). Multi-omics datasets converge on dysregulated stress, repair, apoptotic, immune, and inflammatory programs; epigenetic marks are increasingly considered as substrates for persistent and potentially heritable toxicity, although stable transgenerational transmission remains poorly demonstrated. The review delivers (i) an AOP map with evidence-strength annotations (strong, moderate, emerging), (ii) a structured cross-study synthesis comparing NP and MP effect profiles, and (iii) a critical layer that reinterprets biphasic and apparently contradictory data as mechanistically informative once particle physicochemistry and tissue context are resolved. Progress will depend on standardized characterization, environmentally realistic mixtures, and AOP-anchored designs that distinguish experimentally demonstrated mechanisms from inferred mechanisms and theoretical extrapolations. Full article

Background/Objectives: Waning immunity after primary COVID-19 vaccination supports evaluation of additional doses. HXP-GPOVac is an egg-based, inactivated Newcastle disease virus (NDV)-vectored vaccine expressing a prefusion-stabilized SARS-CoV-2 HexaPro spike antigen. We evaluated the safety, tolerability, and immunogenicity of a single additional 10 µg dose of HXP-GPOVac administered to adults previously primed with two doses of either HXP-GPOVac or BNT162b2. Methods: Study GPO NDV-HXP-S 203 was an open-label phase II extension enrolling adults (18–75 years) who previously completed a two-dose primary series in Study 202 with either HXP-GPOVac or BNT162b2 (Pfizer–BioNTech; Comirnaty). All participants received a single additional 10 µg intramuscular dose of HXP-GPOVac ≥ 6 months after their second primary dose. Solicited local/systemic adverse events (AEs) were recorded for 7 days, unsolicited AEs through Day 28, and serious AEs (SAEs) and adverse events of special interest (AESIs) throughout follow-up. Neutralizing antibody titers (pseudovirus 50% neutralization titer, NT₅₀) and anti-spike IgG (BAU/mL) were assessed pre-dose (Day 1) and post-vaccination through 12 months; a predefined subset underwent IFN-γ and IL-5 ELISpot. SARS-CoV-2 infection during follow-up was assessed using anti-nucleocapsid (anti-N) IgG. Symptomatic COVID-19 was identified through symptom-reported, symptom-triggered RT-PCR testing; sequencing was performed when feasible. Results: All 219 participants received HXP-GPOVac (167 primed with HXP-GPOVac and 52 with BNT162b2). Any solicited local reaction occurred in 22.2% (37/167) of HXP-GPOVac-primed and 26.9% (14/52) of BNT162b2-primed participants; any solicited systemic reaction occurred in 10.8% (18/167) and 13.5% (7/52), respectively. No vaccine-related unsolicited AEs or AESIs were reported. Three deaths occurred during the 12-month follow-up; one (a sudden cardiac death in an HXP-GPOVac-primed participant) was assessed by the safety medical team as possibly related to vaccination, and two were assessed as not related. Neutralizing antibody GMTs increased from 46.33 at baseline to 1569.04 at Day 15 in HXP-GPOVac-primed participants and from 77.25 to 841.34 in BNT162b2-primed participants; corresponding SCRs were 78.8% and 76.9%. Anti-spike IgG GMCs increased from 48.79 to 1480.14 BAU/mL and from 194.48 to 1547.88 BAU/mL, respectively. Responses declined over time but remained above baseline through 12 months. In the cellular immunity subset, post-vaccination IFN-γ responses increased, with comparatively modest IL-5 responses and no pattern suggestive of Th2 predominance. Conclusions: A single additional dose of HXP-GPOVac administered ≥6 months after primary vaccination with HXP-GPOVac or BNT162b2 was generally well tolerated and elicited robust recall humoral responses, with supportive findings of cellular immunity. Trial registration: Thai Clinical Trials Registry, TCTR20230213001. Full article

Global plastic production and inadequate waste management have led to widespread environmental contamination with microplastics (MPs), now detected in food, water, and air. Their small size, diverse polymer composition, and capacity to carry chemical additives and co-pollutants facilitate intestinal uptake and raise concerns about their potential impact on gut microbiota. This review synthesizes current evidence on how MPs influence gut microbial composition and function, gut barrier integrity, and associated inflammatory and metabolic pathways. We conducted a narrative review of in vivo animal studies, in vitro simulated gut systems, and human observational studies that assessed MP exposure, gut microbiota profiles, and downstream toxicological outcomes. MPs originate from primary and secondary sources and can act as vectors for metals and organic pollutants. Following ingestion, they may cross the intestinal barrier via endocytic and persorption routes, acquire a protein corona, and be recognized by immune cells, activating TLR/NF-κB, and MAPK pathways alongside oxidative stress. In these models, MP exposure induces dysbiosis, characterized by loss of beneficial SCFA-producing bacteria (e.g., Bifidobacterium, Lactobacillus, Bacteroides) and expansion of pathobionts (e.g., Escherichia/Shigella, Staphylococcus, Enterobacteriaceae), accompanied by altered bile acid metabolism. These microbiota and metabolic alterations are linked to increased gut permeability, intestinal inflammation, metabolic dysfunction, and, in some studies, reproductive and neurobehavioral effects. Current evidence supports MPs as emerging modulators of gut microbial and intestinal homeostasis. However, heterogeneity across experimental models, reliance on high exposure doses, and lack of standardized MP characterization limit robust risk assessment. These limitations underscore the need for harmonized methodologies, longitudinal large-scale human studies, and the development of targeted mitigation strategies. Full article

Chili products are vulnerable to the addition of unauthorized substances, including Sudan dyes, Rhodamine B, Basic Orange 2, poppy-derived materials and improperly used processing chemicals. Their analysis is complicated by the high contents of lipids, carotenoids, capsaicinoids and other co-extracted matrix components in chili powder, chili oil, chili sauce and composite seasonings. This review critically evaluates conventional and emerging sample-preparation strategies, including solid-phase extraction; the quick, easy, cheap, effective, rugged and safe (QuEChERS) procedure; deep eutectic solvent (DES)-assisted extraction; enhanced matrix removal for lipids (EMR-Lipid); and molecularly imprinted sorbents. Laboratory methods based on high-performance liquid chromatography (HPLC), liquid chromatography–tandem mass spectrometry (LC–MS/MS) and gas chromatography–mass spectrometry (GC–MS) are compared with enzyme-linked immunosorbent assay (ELISA), surface-enhanced Raman spectroscopy (SERS), electrochemical sensors, miniature mass spectrometry and artificial intelligence-assisted hyperspectral imaging (AI–HSI). The comparison considers representative limits of detection and quantification, recovery, precision, sample-preparation burden, cost, portability, validation status and regulatory role. LC–MS/MS remains the preferred confirmatory platform for targeted multi-residue analysis, whereas rapid and portable methods are more appropriate for screening and sample triage. A three-tier workflow linking rapid screening, laboratory confirmation, and emerging-risk identification and traceability is proposed. Future priorities include standardized chili reference materials, open AI training and validation datasets, greener DES-based extraction and interlaboratory validation of field-deployable methods. Full article

Two tri-carbonyl complexes, [Mn(CO)₃(5cpa)Br] (1) and [Re(CO)₃(5cqn)(OCH₃)] (2), were synthesized, where 5cpa is 5-Cl-2-picolinic acid and 5cqn is 5-Cl-8-Hydroxyquinoline. Their structures were determined using X-ray diffraction techniques. The electronic absorption and IR spectra of the complexes were experimentally measured and theoretically assigned through density functional theory (DFT) calculations. The photo-induced CO release was verified using time-resolved infrared spectroscopy, and the transfer of CO to hemoglobin (Hb) was monitored by UV-vis spectroscopy. The rate of CO release and transfer from Mn complex 1 is significantly faster than that from Re complex 2. Complex 2 exhibits higher cytotoxicity against HeLa cells than complex 1, with IC₅₀ values of 40.1 μM and 10.6 μM for 1 and 2, respectively, which decrease to 16.2 μM and 4.9 μM after photo irradiation. Moreover, 1 exhibited a stronger binding constant (K_b) with human serum albumin (HSA) than 2, with values of 1.6 × 10⁶ and 7.0 × 10⁵ M⁻¹, respectively. The structures of HSA complex adducts revealed that both the resulting [Mn(CO)₃(5cpa)]⁻ and [Re(CO)₃(5cqn)]⁻ group coordinate with the N atom of His146, while four additional dissociated Mn-CO groups were observed to bind to HSA for complex 1. This study provides insights into the stability, possible metabolic pathways, and potential applications of these carbonyl complexes. Full article

Background/Objectives: Recent advances in immunotherapy have revolutionized cancer treatment, as exemplified by multiple monoclonal antibodies against programmed cell death protein 1 (PD-1) or programmed death-ligand 1 (PD-L1). Nevertheless, immunotherapeutic antibodies exhibit certain limitations, which drives the development of alternative approaches, such as small interfering RNA (siRNA)-based therapeutics. The aim of this study was to design and produce new biological PD-L1 siRNA (BioRNA/PD-L1-siRNA) molecules and further define their immunotherapeutic efficacy against non-small cell lung cancer (NSCLC) in vitro. Methods: A novel RNA molecular bioengineering platform was employed to produce new BioRNA/PD-L1-siRNA agents. The functions of BioRNA/PD-L1-siRNAs were determined by quantitative PCR, Western blot, immunofluorescence confocal imaging, flow cytometry, and PD-1/PD-L1 blockade assays in human NSCLC cells, alone and co-cultured with human peripheral blood mononuclear cells (PBMCs). Results: After heterologous overexpression and purification of five BioRNA molecules, one siRNA named BioRNA/PD-L1-siRNA-1 was identified as the most effective to selectively suppress human PD-L1 mRNA and protein levels in H460 and H1975 cells. Disruption of PD-1/PD-L1 interactions by BioRNA/PD-L1-siRNA-1 was further demonstrated via a PD-1/PD-L1 blockade bioassay. In addition, the immunomodulatory effectiveness of BioRNA/PD-L1-siRNA-1 was established in co-culture models, as indicated by the induction of T-cell and natural killer cell populations and an increase in specific cytokines and cytotoxic granules, and subsequent enhancement of apoptosis and greater inhibition of NSCLC cell viability. Conclusions: Overall, these findings demonstrate the potential of bioengineered PD-L1 siRNA entities for NSCLC immunotherapy. Full article

Background/Objectives: Pancreatic ductal adenocarcinoma (PDAC) is a lethal malignancy with a desmoplastic, immunosuppressive tumor microenvironment enriched in extracellular adenosine. High adenosine levels disrupt anti-tumor immunity by engaging adenosine receptors on T cells, macrophages, and dendritic cells. In this context, strategies to reduce extracellular adenosine signaling within the TME are in focus. Among them, enzymatic degradation of extracellular adenosine levels has emerged as a promising approach to overcome immune suppression and restore anti-tumor immune responses. Methods: Here, we engineered an E. coli strain to express a surface-bound form of a bacterial ADA2 enzyme and used the outer membrane vesicles produced by this strain as nanoparticles carrying the functional enzyme. Our data indicate robust surface expression and enzymatic activity of ADA2 on OMV particles. Results: In a PDAC subcutaneous flank tumor model, intratumoral administration of OMV-ADA2 particles was associated with significantly increased infiltration of CD8⁺ T cells and Granzyme B expression and concomitant decreases in collagen deposition and α-smooth muscle actin (α-SMA) positive stromal cells, suggesting modulation of the desmoplastic stroma. Conclusions: These findings support further investigation of OMV–bADA2 as a potential platform to modulate tumor metabolism and stroma, activate anti-tumor immunity, and serve as a carrier for co-delivery of additional anticancer modalities in PDAC. Full article

Background/Objectives: Tubulins (Tub) are central components of microtubules, but intraspecific variation and developmental expression of the Tub family in Gossypium barbadense remain poorly characterized. This study aimed to characterize the GbTub family using a pan-genome framework and identify candidates associated with fiber development and strength. Methods: A total of 50 GbTub genes were identified in the G. barbadense 3-79 reference genome, and their orthologous presence–absence patterns were subsequently assessed across 12 additional G. barbadense accessions. Phylogenetic, presence–absence variation (PAV), Ka/Ks, structural variation (SV), RNA-seq, RT-qPCR, co-expression, and GO enrichment analyses were integrated. Results: Among the 50 reference-defined GbTub genes, 43 were classified as core genes, 6 as near-core genes, and 1 as an accessory gene, and the encoded proteins were classified into α-, β-, and γ-tubulin clades. All genes showed Ka/Ks < 1. Twenty-three GbTub genes differed between the fiber-strength-contrasting accessions 5917 and PimaS-7, and representative expression trends were supported by RT-qPCR. Network analysis prioritized 10 GbTub candidates based on degree centrality. GbTub21 was the sole SV-associated GbTub gene displaying significant differential expression between accessions harboring versus lacking the corresponding SV. Non-Tub neighbors of the candidate hub genes were enriched for cytoskeletal, intracellular-transport, and plasma-membrane functions. Conclusions: The pan-genome analysis reveals strong conservation with limited intraspecific variation in the GbTub family. Co-expression profiles nominate candidates associated with fiber secondary-wall development, and their causal contribution to fiber strength awaits functional dissection. Full article