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Biology subjects

Zhu, X.

Publications and source records attributed to Zhu, X..

At least 55 records · Page 3Linked to original sources

CHORD: a framework for cross-species single-cell integration across gene, cell and cell-type levels

Quantifying cross-species relationships among cell types from single-cell transcriptomic data can reveal both conserved and divergent patterns of cell-type hierarchies. However, existing cross-species integration methods can be limited in modeling genes beyond orthologs by leveraging cell-type-resolved transcriptional context, or in learning explicit type-level representations. Here we present CHORD, a cross-species integration framework that jointly learns representations of genes, cells and cell types. We demonstrate that CHORD can integrate cross-species single-cell atlases and support cell-type annotation with unknown cell-type detection. In the frog-zebrafish embryogenesis and mammalian motor cortex atlases, CHORD infers cell-type trees that place conserved cell types from different species in relative proximity and summarize hierarchical relationships among cell types. CHORD also supports cross-species comparison of continuous phenotypic variation by placing embryonic cells along an aligned developmental timeline. CHORD further yields gene embeddings that capture orthologous and functional relationships, and gene importance scores linking genes to cell types.

bioinformatics↗

Zebrafish Functional Screening of FDA-Approved Drugs for Autosomal Dominant Retinitis Pigmentosa Caused by RHODOPSIN Q344X Mutation

Retinitis Pigmentosa (RP) is a group of inherited retinal degenerations for which most subtypes lack effective drug treatments. This challenge is particularly critical for autosomal dominant (ad) RP, which is often unsuitable for gene replacement therapy. To address this challenge, we screened an FDA-approved compound library using a zebrafish adRP model expressing a human RHODOPSIN transgene with the Q344X mutation. The screen evaluated drug effects on larval visual behavior by assessing the visual-motor response (VMR). Four compounds significantly improved VMR in Q344X zebrafish: amitriptyline, difluprednate, maprotiline, and prednisolone. Further characterization revealed that these hits act through distinct mechanisms, including reducing rod death, promoting rod neogenesis, and enhancing the function of extraocular photoreceptors. Together, these findings demonstrate the potential to repurpose these drugs for adRP caused by the RHO Q344X mutation, providing preclinical candidates and revealing potential targets for future drug development.

neuroscience↗

TopicVI: A Knowledge-guided deep interpretable model for resolving context-specific gene programs

Mechanistic insights from single-cell and spatial transcriptomics largely rely on cell clustering, differential expression analysis, and interpretation through prior biological knowledge. However, this approach is often limited by the reliance on curated biological priors that fail to capture context-specific gene programs, particularly in complex disease states. To address this gap, we introduce TopicVI, a deep interpretable model that integrates established biological knowledge with data-driven refinement to discover context-dependent gene programs in single-cell and spatial transcriptomic data. TopicVI jointly infers cell clusters and gene topics using optimal transport to flexibly align prior gene programs with observed data while permitting context-specific refinements. Comprehensive benchmarking demonstrates that TopicVI outperforms existing methods in biological conservation, batch correction, topic coherence, and rare cell identification. TopicVI effectively disentangles multiple sources of biological variation, such as separating anatomy-specific expression patterns from disease-associated signatures in spatial transcriptomics. Applying TopicVI to glioblastoma datasets, we identify gene topics related to cell cycle regulation and EGFR signaling that reveal convergent tumor states across distinct drug perturbations. By integrating prior knowledge with data-driven discovery, TopicVI enables identification of interpretable gene programs that illuminate biological processes and therapeutic mechanisms in complex transcriptomics data.

bioinformatics↗

PRISM: A High-Throughput Simulation Infrastructure for CADD Agents

Despite rapid progress in AI agents for computer-aided drug design (CADD), protein-ligand simulation workflows remain fragmented across disparate tools, creating a major bottleneck for scalable candidate evaluation. Here, we present PRISM (Protein-Receptor Interaction Simulation Modeler), a Python platform built on GROMACS that unifies ligand parameterization across multiple force fields, automated system construction, enhanced sampling, multi-tier binding free energy estimation, and trajectory analysis within a single workflow. Through the Model Context Protocol (MCP), PRISM further serves as the computational infrastructure for CADD-Agent, an expert-workflow-driven AI agent designed to orchestrate hierarchical drug screening pipelines. As a pilot application, we applied PRISM to riboflavin synthase and demonstrated end-to-end automation from candidate library assembly to binding pocket characterization, identifying a potential allosteric inhibition site at the oligomerization interface. Together, these results establish PRISM as a high-throughput simulation infrastructure for agent-enabled CADD.

biophysics↗

MCM10 and RECQL4 have cooperative and redundant roles in activating the CMG helicase during the replication initiation

DNA replication initiation requires activation of the CMG helicase to establish the replisome. This process involves the extrusion of single-stranded DNA (ssDNA) from the central channel of MCM double hexamers, allowing the two CMG helicases to pass each other; however, the factors that mediate this process in human cells remain unclear. We show that degron-mediated depletion of either MCM10 or RECQL4 alone causes only mild replication defects, whereas simultaneous depletion of both proteins completely blocks CMG activation. ChIP-seq analyses demonstrate that RECQL4 localises to replication initiation zones (IZs) independently of MCM10, whereas MCM10 recruitment to IZs is enhanced upon RECQL4 depletion, suggesting RECQL4 primarily functions in CMG activation, and MCM10 acts as a backup or supporting factor. Rescue experiments further indicate that RECQL4 cooperates with MCM10 through direct interaction, and that their ssDNA-binding activity underlies their functional overlap. We propose MCM10 and RECQL4 act cooperatively and redundantly to promote CMG activation.

molecular biology↗

Therapeutic targeting inflammation linking periodontitis and atherosclerotic comorbidities using cell-free DNA-capturing nanomaterials

Periodontitis-associated systemic inflammation makes it a great challenge to explore therapeutic options applicable to periodontitis and atherosclerotic comorbidities. Here, we identify the crucial role of cell-free DNA (cfDNA) that underlies these comorbidities. Hypothesizing cfDNA as a therapeutic target, we engineer polyamidoamine dendrimer-functionalized nanomaterials to modulate such local-systemic inflammatory crosstalk. Periodontium-originated DNA can be systemically captured by cationic nanomaterials, and capturing cfDNA, whether locally or systemically, alleviates both periodontitis and atherosclerosis prior to severe atherosclerotic development in vivo. The transcriptomic and single-cell RNA sequencing analyses together reveal that cfDNA-capturing nanomaterials regulate inflammatory foam cell transformation in macrophages by modulating the expression of lipid-related foamy markers Spp1 and Fabp4. This study provides a proof of concept for cfDNA-driven periodontitis-atherosclerosis crosstalk, and offers a cfDNA-capturing nanoplatform for therapeutic intervention targeting periodontitis and atherosclerotic comorbidities in a holistic fashion.

immunology↗

Sex-specific Genetic Regulatory Effects in Chickens

Sexual dimorphism is a defining vertebrate feature, yet its sex-specific molecular architecture remains poorly understood. Here we established a sex-balanced, uniformly reared chicken cohort to map this landscape, integrating individual whole-genome sequencing with 7,969 bulk and 779,380 single nucleus transcriptomes across 32 tissues from 280 birds. We identified 495,098 independent expression quantitative trait loci for 20,194 genes, including 10,937 loci modulated by cell-type composition. Notably, 340 genes were regulated by 449 loci in a sex-dependent manner, significantly enrichment in endocrine tissues like adipose and the adrenal gland. Furthermore, we fine-mapped 1,219 structural variants, demonstrating their unique roles to tissue- and sex-specific expression beyond SNPs. Ultimately, we showed the utility of these regulatory effects in elucidating the molecular basis of metabolism and complex traits in both chickens and humans. This comprehensive atlas of regulatory effects provides profound insights into the genomic and molecular basis of sexual dimorphism in vertebrates.

genomics↗

Multi-agent reasoning enables predictive design of living materials

Artificial intelligence is increasingly used to accelerate scientific discovery, but most successful frameworks operate within well-defined molecular, protein or materials spaces. Living materials present a more formidable computational problem because functions emerge from context dependent coupling among cells, matrices, fabrication processes and evaluation conditions. Here we introduce LiveMat, a multi-agent reasoning framework that transforms unstructured literature into a computable design space for living materials. LiveMat standardizes 34,215 living material records, integrating 16,769 microorganism and 17,446 polymer entries into a knowledge graph linking living components, abiotic matrices, functional outputs, evaluation contexts and performance metrics. Benchmarking across five large language models shows that living material reasoning is limited mainly by cross-domain feature integration rather than coarse classification. LiveMat overcomes this limitation through constraint decomposition, provenance-aware extraction, consistency checking and expert-anchored ranking. In a prospective wound-healing task, it prioritizes a four-component design with state-of-the-art in vivo performance, establishing a scalable infrastructure for interpretable, evidence-grounded living material discovery.

biochemistry↗

Proteomic composition and mutual assembly of the C2a projection in vertebrate motile cilia

The central apparatus of motile cilia, consisting of central microtubules and various protein projections, is essential for dictating the ciliary movement. Although three proteins (FAP65, FAP147, and FAP70) have been localized to the C2a projection in Chlamydomonas reinhardtii, the full protein composition and functional roles of the vertebrate C2a remain inadequately defined. Here, we use three knockout mouse models corresponding to their respective homologs (Ccdc108, Mycbpap, and Cfap70) to systematically investigate their functions in vertebrates. Notably, all three knockout strains exhibit distinct phenotypes related to primary ciliary dyskinesia (PCD), including hydrocephalus and sinusitis. The ciliary incorporation of CCDC108, MYCBPAP, and CFAP70 is essential for one anothers stability, with the loss of any single component triggering C2a collapse, which destabilizes the central pair microtubules and ultimately alters the ciliary movement pattern. Furthermore, we significantly expand the vertebrate C2a proteome by identifying ARMC3 and MYCBP as additional C2a components. Collectively, our findings illuminate the proteomic composition and strict physiological requirements of the vertebrate C2a projection, providing new insights into the molecular pathogenesis of PCD. Impact StatementDeficiency in any of the interdependent C2a proteins (CCDC108, MYCBPAP, and CFAP70) collapses this central pair microtubule-associated projection, disrupting vertebrate ciliary movement and causing primary ciliary dyskinesia phenotypes in mice.

cell biology↗

Loss of α2,3-linked sialoside in the receptor-binding site of a H5N1 influenza hemagglutinin identified in a human patient

In November 2024, an adolescent female in British Columbia was hospitalized presenting with severe symptoms including respiratory failure due to infection with a novel H5N1 subtype influenza strain (BC24). Using cryogenic electron microscopy (cryo-EM), we show here that the N169 2,3-linked auto-glycan that is found in the sialic acid binding site of previously studied H5 hemagglutinin (HA) proteins is absent in purified BC24 HA protein, suggesting greatly reduced affinity for 2,3-linked sialosides. Glycan microarray analysis shows that the BC24 HA protein displays reduced or no binding not just to most 2,3-linked sialosides, but also to 2,6-linked sialosides. Full-length BC24 HA expressed in A549 lung alveolar carcinoma cells drives membrane fusion, albeit at significantly lower levels than previous H5 HA proteins, and post-infection sera from the patient display strong binding to BC24 HA and HA proteins from other influenza subtypes. The high virulence of the BC24 strain despite weak receptor binding reveals further complexity in the factors that result in severe disease caused by avian influenza.

biochemistry↗

Complement Factor H (Y402H) polymorphism for age-related macular degeneration alters retinal lipids

Age-related macular degeneration (AMD), the leading cause of blindness in the elderly, is associated with multiple risk factors and involves death of the retinal pigment epithelium (RPE). We investigated how the Y402H polymorphism of Complement Factor H (CFH) and cigarette smoke extract (CSE), major AMD genetic and environmental risks, affect lipid metabolism in RPE differentiated from induced pluripotent stem cells (iPSC-RPE) that were derived from human donors genotyped for low-risk (LR) or high-risk (HR) CFH. Results from discovery-based (lipidomics, proteomics) and targeted (mitochondrial fatty acid oxidation (FAO)) assays found significant genotype-dependent differences under basal conditions include higher free fatty acids and cholesterol esters in HR cells. CSE induced differences in proteins regulating lipid handling, lipolysis, and inflammation. Lower FAO in HR cells was observed in multiple donors and pairs of parent/isogenic edited lines compared with LR lines. CSE induced lipid accumulation, lipid composition remodeling, and upregulation of proteins involved in lipid synthesis/hydrolysis, production of bioactive lipid mediators, and metabolism of ceramide and cholesterol. These results elucidate putative mechanisms driving pathology in RPE harboring CFH Y402H.

systems biology↗

MR-μScope: a multi-scale and simultaneous MRI-miniaturized microscopy system for elucidating neurovascular coupling

Blood Oxygen Level Dependent functional MRI (BOLD-fMRI) revolutionized non-invasive brain mapping, yet the physiological origins of its signal, linking microscopic neurovascular activity to macroscopic hemodynamics, remain elusive. To bridge this gap, we developed MR-Scope: a simultaneous and multimodal platform that integrates preclinic high-field MRI (9.4T) and miniaturized fluorescence microscopy (Miniscope). Our system contains an MR-compatible Miniscope with electromagnetic shielding, a customized radiofrequency coil with a central optical window, and an adjustable animal cradle, enabling artifact-free acquisition of whole-brain fMRI alongside microscopic vascular dynamics. Phantom validation confirmed negligible cross-modal interference (fMRI SNR [≥] 15 dB; optical SNR [≥] 26 dB). MR-Scope captured stimulus-evoked microvascular dilation and blood flow velocity changes in the somatosensory cortex concurrent with BOLD signals, revealing vessel-size-dependent neurovascular coupling. MR-Scope provides an effective solution for deciphering multi-scale neurovascular interactions and offers unique potential for advancing research into brain function and disease mechanisms involving vascular pathology.

bioengineering↗

Focused ultrasound programmed characteristic NIR-IIb lanthanide mechanoluminescence for high sensitivity bioimaging in vivo

Optical imaging techniques for biodetection are hindered by limited sensitivity and resolution in deep tissues, arising primarily from photon scattering and endogenous autofluorescence. Herein, we report a focused ultrasound (FUS) programmable NIR-IIb emissive mechanoluminescent nanoparticle for in vivo bioimaging. Specifically, CaZnOS nanoparticles co-doped with Mn2+ and Er3+ were engineered to exhibit mechanoluminescence (ML) emission peaked at 1550 nm. FUS stimulation elicits ML without the need for optical excitation, thereby enabling deep-tissue imaging devoid of background interference from excitation light. By modulating the excitation frequency of FUS, ML can be programmed as a characteristic signal. Integrated with a Fourier frequency-transform identification reconstruction (FFIR) algorithm, the specific ML signals can be detected with high sensitivity, reaching sub-millimeter spatial resolution and markedly enhanced signal-to-background ratios compared to conventional photoluminescence-based approaches. By macrophage internalization of the ML nanoparticles to yield functional macrophage-nanoparticle (FMNs), a ultralow detection limit of 10 cells can be achieved. In murine tumor models, the FMNs facilitated real-time monitoring of early-stage tumor progression, underscoring their biocompatibility and translational promise for high-precision diagnostics in deep-seated neoplasms.

bioengineering↗

Identification and Regulation of a Hepatic Lipogenic Metabolon

De novo lipogenesis (DNL) plays a key role in the excessive fat accumulation present in Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD). Most mechanistic studies and experimental strategies for improving hepatic steatosis in MASLD have focused on the transcriptional regulation of enzymes involved in DNL and triglyceride (TG) synthesis. Here, we provide evidence for a post-translational mechanism that enhances fatty acid (FA) and TG synthesis through the assembly of a multi-protein lipogenic metabolon in liver. Under anabolic conditions, acetyl-CoA carboxylase 1 (ACC1) interacts with additional key enzymes in the DNL and TG synthesis pathway. Immunofluorescence and electron microscopy reveal that this lipogenic metabolon localizes around lipid droplets (LDs) and in proximity to mitochondria and LD interfaces in the anabolic state. The formation of the lipogenic metabolon facilitates the efficient transfer of FA synthesis intermediates to enhance lipogenic flux. These findings uncover a new nutrient-responsive, post-translational regulatory mechanism for hepatic lipogenesis and highlight the lipogenic metabolon as a potential therapeutic target for metabolic liver diseases.

cell biology↗

A multilevel hierarchical framework for quantification of experimental heterogeneity

Biological systems exhibit substantial heterogeneity: that is, variation in specific characteristics of individuals within a population. As a result, it is of critical importance to appropriately account for biological heterogeneity when calibrating mathematical models to infer cellular processes and predict behaviour. Recent approaches consider ordinary differential equations with random parameters to quantify heterogeneity in dynamical processes of cells. In this setting, statistical inference is performed to characterise the distribution of these random parameters within a cell population. One significant limitation of this approach is the tacit assumption that there are no substantial deviations in these distributions across experimental replicates. In this work, we propose a flexible Bayesian hierarchical differential equation modelling framework that quantifies and distinguishes both inter-experimental heterogeneity (heterogeneity between experimental replicates) and intra-experimental heterogeneity (biological heterogeneity within replicate populations). We consider two recent studies that employ mathematical models to interpret flow cytometry snap-shot data and quantify heterogeneity in nano-particle cell interactions and cell internalisation processes. Using simulation data, we demonstrate that substantial inaccuracy in the inferred dynamics can arise when experimental heterogeneity is not accounted for. By contrast, our hierarchical approach is robust to variability in inter-experimental and intra-experimental heterogeneity and our method simplifies to previous methods when inter-experimental heterogeneity is negligible. Our approach is flexible and widely applicable to applications involving replicate populations and snapshot data.

cell biology↗

Spatial Regulation of Lysosomal Vesicle Acidification Along the Axon via mRAVE-Dependent v-ATPase Assembly

Lysosomal acidification is essential for neuronal homeostasis, supporting degradative clearance and metabolic signaling in all neuronal domains. Yet, how lysosomal acidification is spatially regulated within neurons remains unclear. Here, we show that assembly of the membrane-embedded V0 and cytosolic V1 domains of the vacuolar H-ATPase (v-ATPase) -- the proton pump that drives lysosomal acidification -- governs spatial and functional lysosome diversity. In non-neuronal cells, V1-V0 association is higher in perinuclear lysosomes, correlating with increased acidity of this population. In neurons, axonal V0-positive vesicles move bidirectionally, whereas V1-V0 -positive vesicles move almost exclusively in the retrograde direction, consistent with the higher acidity of retrograde lysosomal vesicles. Depletion of DMXL2, a subunit of the mRAVE complex that promotes V1-V0 assembly, reduces V1 association, acidification, transport, and proteolytic activity of retrograde lysosomal vesicles in the axon. Together, these findings reveal a spatially regulated mechanism for the acidification of axonal lysosomal vesicles and identify mRAVE-dependent v-ATPase assembly as a key determinant of this process. Subjects: Organelles, Trafficking, Disease

cell biology↗

Licoisoflavone A improves adipose tissue dysfunction in response to diet induced obesity by promoting METTL3 expression

As developing obese adipose tissue, adipocytes suffer pathological changes from inert energy storage to excessive and active endocrine organ in association with disease hazard. METTL3, as an RNA methyltransferase of key importance in adipose tissue development, functional preservation and metabolic homeostasis, is remarkably complex. Licoisoflavone A (LIC-A) is a prenylated flavonoid compound of licorice that has been suggested to display antiinflammatory, -hypertrophic, and -proliferative activities; it remains unknown whether it can directly modulate expression of METTL3 and impact functions of adipose tissue in obesity. Here in our study, 16 candidates in the top ranking molecules were screened out in the process of the molecular docking between our TCM formula Fangjihuangqin Decoction and protein METTL3 (PDB: 5TEY). Among them, LIC-A was considered as a potential upstream regulatory molecule of METTL3 and obviously promote the expression of METTL3. The effects of TNF- and LPS treatments on the inhibition of adipogenesis were successfully recovered by LIC-A treatment in the adipogenic 3T3-L1 cells, via the regulation of adipogenic cytokines, as well as the expression of inflammatory factors. These protective effects were similarly abolished with METTL3 knockdown, suggesting the role of LIC-A relies on METTL3. Moreover, in vivo data demonstrated that administration of LIC-A could significantly recover the body weight lipid metabolism, insulin resistance and gluconeogenesis in mice with reduced adipose depostion as well as abated systemic inflammation. In conclusion, our study suggested that LIC-A could be the key component in preserving the homeostasis of adipose tissues through regulating METTL3 expression, indicating LIC-As promising treatment potential for obesity-related metabolic diseases.

pharmacology and toxicology↗

DeepDOX1: A Dual-Drive Framework Integrating Deep Learning and First-Principles Physics for Drug-Protein Affinity Prediction

In this work, we present DeepDOX1, a dual-drive drug-protein affinity (DPA) prediction tool features the tight integration of a concise AI architecture and a quantum mechanics based representation. The first-principle physics generated features incorporating the interactions between the drug and the protein pocket allows a relatively simple CNN model trained on a relatively small training set to exhibit exceptional generalization capabilities across extensive testing. Notably, DeepDOX1 outperforms popular AI models in the tests simulating real-world drug design scenario and a highly challenging test set featuring covalent ligands, halogenated ligands and metalloproteins. In addition, we designed a series of novel covalent inhibitors targeting the diabetes target hu-FBPase using DeepDOX1. Subsequent experimental validation including enzyme-level bioactivity assays and crystal structure determination confirmed the DeepDOX1s effectiveness in real-world drug design applications. It is conceivable that the combination of AI and first-principle QM might be one of the next breakthrough points of DPA prediction.

bioinformatics↗