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Biology subjects

Yang, Z.

Publications and source records attributed to Yang, Z..

At least 109 records · Page 6Linked to original sources

GCN-Mamba: Graph Convolutional Network with Mamba for Antibacterial Synergy Prediction

The escalating crisis of antimicrobial resistance necessitates novel therapeutic strategies, among which drug combination therapy shows great promise by enhancing efficacy and reducing toxicity. However, identifying effective synergistic pairs from the vast combinatorial space remains experimentally challenging and resource-intensive. To address this, we introduce GCN-Mamba, a deep learning framework that integrates Graph Convolutional Networks (GCN) with the Mamba State Space Model. This architecture captures both local molecular topological structures and global implicit interactions by leveraging Extended 3-Dimensional Fingerprints (E3FP) and bacterial gene expression profiles. Evaluation on a comprehensive dataset demonstrated that GCN-Mamba significantly outperforms classical machine learning models in predictive accuracy. In a targeted case study against Methicillin-resistant Staphylococcus aureus (MRSA), the model successfully rediscovered known synergistic pairs, such as Quercetin and Curcumin, consistent with recent literature. Furthermore, prospective in vitro validation confirmed a novel synergistic combination of Shikimic acid and Oxacillin, validating the models practical utility. By efficiently prioritizing potential candidates, GCN-Mamba serves as a powerful and reliable tool for accelerating the discovery of synergistic antimicrobial combinations, effectively bridging the gap between computational prediction and experimental validation.

bioinformatics↗

IL12-engineered human PSMA-CAR T cells for the treatment of advanced prostate cancer

Adoptive cell therapies used to treat advanced prostate cancer are being developed to target several tumor-associated antigens, including prostate-specific membrane antigen (PSMA). Chimeric antigen receptor (CAR) T cell therapy using the single chain variable fragment (scFv) derived from the humanized murine mAb clone, J591, as the antigen-binding domain has shown promising anti-tumor activity. However, it has also been associated with macrophage activation syndrome and other unwanted toxicities, highlighting the need for more specific and human-derived antigen-binders with optimized construct designs for improved safety and efficacy. Here, we optimize a human scFv-based PSMA-targeted CAR (hPSMA-CAR) with highly selective PSMA targeting. We further introduce a membrane-bound IL-12 (mbIL12) molecule, which enhances potency with increased T cell expansion, IFNy production and anti-tumor cell activity in vitro. Using two clinically-relevant bone-metastatic prostate cancer models, we show that mbIL12-engineered hPSMA-CAR T cells drive potent in vivo anti-tumor responses. In summary, we have developed a promising therapeutic that has potential to promote safe and effective treatment of advanced PSMA+ prostate cancer.

bioengineering↗

A stable subgenomic reporter coronavirus enables transcriptional profiling of bystander cells.

Insertion of fluorescent reporter genes into viral genomes is a powerful tool for monitoring infection. In coronaviruses, this is commonly achieved by replacing accessory open reading frames, thereby deleting endogenous gene functions. An alternative strategy is to manipulate viral RNA synthesis by inserting copies of the viral transcription regulatory sequence (TRS) which drive the transcription of viral subgenomic RNAs. However, coronavirus transcription is tightly regulated, and these modifications frequently disrupt native subgenomic RNA synthesis and attenuate viral growth. Here, we describe a reporter coronavirus that overcomes these limitations. Using human coronavirus (HCoV)-OC43 as a model system, we inserted an mNeonGreen reporter between the Spike and ORF5 coding regions, engineering the TRS and surrounding sequence to minimise off-target effects to transcription. This virus is genetically stable, with wildtype growth kinetics and unaltered subgenomic RNA transcriptional ratios. We developed a flexible reverse genetics system, which allows rapid cloning and virus recovery, supported by optimised HCoV-OC43 culture conditions, for high-titre stock generation, and validated analytical reagents. Our reporter virus enabled sensitive detection and isolation of infected cells, facilitating transcriptomic analyses that distinguish host responses in infected and bystander populations. We found that transcriptional responses to infection of cells in culture were predominantly inflammatory, rather than interferon-mediated, and that bystander cells upregulated pathways associated with cytokine response signalling and cell-cell contact sensing. Together, these tools expand the experimental utility of HCoV-OC43, an important seasonal respiratory pathogen and low containment model for betacoronavirus biology.

microbiology↗

Quantitative dissection of the metastatic cascade at single colony resolution

Metastasis is the leading cause of cancer-related deaths. However, the core determinants and mechanistic principles underlying the metastatic cascade remain elusive. Small cell lung cancer (SCLC) is a highly aggressive malignancy with exceptional metastatic potential and limited therapeutic options. Here, we present Metastasis Originated Barcode Sequencing (MOBA-seq), a high-throughput in vivo platform that systematically maps genetic regulators across the metastatic cascade at single-colony resolution. MOBA-seq integrates scalable barcode-based lineage tracing with a computational pipeline that quantitatively deconvolutes genotype-specific effects on metastatic seeding, dormancy, and clonal expansion across hundreds of thousands of metastatic events. Applying this approach to more than 400 candidate regulators of SCLC, we uncovered tissue-specific metastatic suppressors and universal metastatic essential genes. We identified metastatic seeding as the predominant determinant of metastasis. Comparative analysis across recipient mice of distinct genetic backgrounds further revealed that innate immune surveillance constrains metastatic progression by reducing metastatic seeding and enforcing dormancy, with additional modulation by sex and tissue context. We validated the frequently mutated gene CREBBP as a key metastasis suppressor whose loss enhances SCLC metastasis through both tumor-intrinsic and immune-modulatory mechanisms. This work establishes a scalable and quantitative platform for mapping the metastatic fitness landscape at single-colony resolution across hundreds of thousands of in vivo data points. Our approach offers a broadly applicable framework for dissecting the interactions between cancer-intrinsic and microenvironmental factors governing tumor initiation, progression, and therapeutic response.

cancer biology↗

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↗

What and where manifolds emerge and align with perception in deep neural network models of sound localization

Whether the auditory cortex has parallel pathways for sound identification ("what") and localization ("where"), and whether it contains a map of auditory space, is debated. Here, we examined the low-dimensional structure (manifold) of "what" and "where" representations in deep neural network models of sound localization. Unexpectedly, models trained for "where" learned untangled "what" manifolds, including voice type, reverberation, and spectral detail. The distribution of "what" manifolds was not random, but geometrically organized by spectral similarity. The separability and distance of both "what" and "where" manifolds were aligned with human behavior. "What" also determined whether "where" manifolds organized into a map: maps emerged when "what" contained localization cues that were topographically organized. However, forming a spatial map reduced localization accuracy in both models and human listeners. Together, object manifolds reveal learned task-irrelevant attributes of object that are ignored when measuring task performance alone, and task-optimized neural networks can provide insights into brain and behavior, not just replicate them.

neuroscience↗

AI-driven discovery and engineering of human endogenous nanocage proteins for mRNA delivery

Safe and effective gene delivery remains a central challenge for therapeutic applications. While non-viral and viral vectors have enabled substantial progress, their reliance on non-human components often triggers immune responses, limiting their use in chronic treatments. Here, we developed DeepDelivery, an artificial intelligence-driven platform to repurpose human proteins for mRNA delivery. An unbiased screening of the human proteome nominated 512 candidates, with experimental validation confirming that 80% of top-ranked hits form mRNA-encapsulating particles and mediate efficient functional delivery in human cells without provoking detectable inflammation. Notably, multiple tripartite motif (TRIM) family proteins, typically linked to antiviral responses, exhibited strong assembly and delivery activity. Quantitative analysis and interpretation of the model revealed structural domains that govern nanocage formation, enabling domain-guided engineering of TRIM25 variants with enhanced function. Our work establishes a generalizable framework for discovering human-derived delivery vehicles and provides a path toward programmable, non-immunogenic mRNA therapeutics.

synthetic biology↗

Engineered probiotics for tumor-targeted combination chemoimmunotherapy

Achieving tumor-specific delivery and sustained activation of both cytotoxic and immune-modulating agents remains a critical challenge in chemoimmunotherapy. Here, we present a bacterial platform engineered to combine enzyme/prodrug chemotherapy with immunotherapy, where tumor-homing E. coli Nissle 1917 expresses cytosine deaminase to convert the prodrug 5-fluorocytosine into the cytotoxic drug 5-fluorouracil within tumors. Concurrently, the engineered bacteria produce an IL-15 superagonist and a PD-L1 blocking nanobody to mitigate the immunosuppressive effects of tumor-localized chemotherapy. This platform demonstrated potent antitumor effects in the murine MC38 solid tumor model. Mechanistic studies showed that the combination therapy enhances activation of antigen-presenting cells, T cells and natural killer cells, while reducing immunosuppressive populations. In summary, our approach integrates enzyme/prodrug therapy and immunotherapy into a single bacterial delivery system, overcoming the limitations of conventional therapies and offering a scalable and precision-engineered strategy with an improved safety profile for synergistic cancer treatment. One Sentence SummaryA precision-engineered bacterial platform integrates enzyme/prodrug chemotherapy and immunotherapy to drive synergistic antitumor responses with enhanced safety, offering promise for clinical translation.

cancer biology↗

Mutant FGFR3 restricts bone yet expands cortex via ERK-mediated self-repression

FGFR3 gain-of-function mutations cause achondroplasia 1,2, the most common form of dwarfism, yet trigger paradoxical cerebral overgrowth and skeletal stunting 3-9. Here, we demonstrate that Fgfr3-K644E mutant drives enhanced ERK activation, which then represses Fgfr3 expression and downregulates ERK signaling. In the developing cortex, this mechanism transiently expands cortical stem cells by activating ERK, then shifts signaling to downregulate Fgfr3/ERK/PKA and enhance YAP/TAZ, promoting cerebral overgrowth and premature ependymal maturation. In growing bones, Fgfr3-K644E mutant first elevates ERK to inhibit chondrocyte pre-hypertrophy, then downregulates Fgfr3/ERK/PKA and upregulates YAP/TAZ to accelerate premature hypertrophy and ossification. Our findings establish that FGFR3 mutations limit bone yet expand cortical size via an ERK negative feedback loop, revealing a unified disease mechanism and novel therapeutic targets.

developmental biology↗

Detection of Somatic Point Mutations Directly from Spatial Transcriptomics Enables in vivo Spatiotemporal Lineage Tracing

Spatial transcriptomics reveals tissue organization but lacks in vivo lineage-tracing methods applicable to humans. We introduce SpaceTracer, a computational framework that accurately detects somatic single-nucleotide variants (SNVs) directly from spatial transcriptomics data. By leveraging naturally occurring somatic SNVs, SpaceTracer reconstructs cellular phylogenies within native tissue architecture, enabling the mapping of lineage spread, migration, lineage-coupled expression changes and lineage-aware local interactions. Applied to human cutaneous squamous cell carcinoma, it traced tumor initiation and progressions, uncovered widespread pre-invasive migration of dedifferentiated epithelial cells and characterized mutant B cells migrating from tertiary lymphoid structures (TLS) into the tumor boundary. The framework also reconstructed developmental lineages across multiple tissues and identified tissue-resident mutant immune cells. SpaceTracer thus provides a perturbation-free platform for high-resolution spatiotemporal lineage tracing, offering a transformative tool for elucidating complex biological systems--especially tumor-immune ecosystems--with direct implications for advancing cancer immunotherapy.

bioinformatics↗

PhyloSOLID: Robust phylogeny reconstruction from single-cell data despite inherent error and sparsity

While lineage tracing based on somatic mutations in single-cell sequencing data offers a powerful approach to reconstructing cellular histories in vivo, its reliability is fundamentally limited by pervasive technical artifacts--specifically, high error rates and data sparsity. These issues introduce false phylogenetic signals that corrupt tree topology and lead to spurious evolutionary conclusions. To overcome these limitations, we present PhyloSOLID, a phylogenetic algorithm designed to be inherently robust to these data imperfections. PhyloSOLID employs a progressive scaffolding strategy that begins with graph-based construction of a low-resolution, high-confidence backbone tree from reliable and uniformly covered mutations. This scaffold is then refined through the iterative integration of remaining data, guided by a Bayesian statistical model that penalizes phylogenetic inconsistencies to effectively separate the true evolutionary signal from technical artifacts. Benchmarking on both simulated datasets and multiple ground-truth datasets demonstrates that PhyloSOLID achieves superior lineage reconstruction accuracy over existing methods, for both single-cell RNA-seq and DNA-seq data. Additionally, a user-friendly web interface enables customized quality assessment, artifact removal, and interpretation of lineage structures. PhyloSOLID provides a powerful solution for decoding cellular evolution in developmental and disease contexts.

bioinformatics↗

ImmunoPheno: A Computational Framework for Data-Driven Design and Analysis of Immunophenotyping Experiments

Immunophenotyping is fundamental to characterizing tissue cellular composition, pathogenic processes, and immune infiltration, yet its accuracy and reproducibility remain constrained by heuristic antibody panel design and manual gating. Here, we present ImmunoPheno, an open-source computational platform that repurposes large-scale single-cell proteo-transcriptomic data to guide immunophenotyping experimental design and analysis. ImmunoPheno integrates existing datasets to automate the design of optimal antibody panels, gating strategies, and cell identity annotation. We used ImmunoPheno to construct a harmonized reference (HICAR) comprising 390 monoclonal antibodies and 93 human immune cell populations. Leveraging this resource, we algorithmically designed minimal panels to isolate rare populations, such as MAIT cells and pDCs, which we validated experimentally. We further demonstrate accurate cell identity annotation across publicly available and newly generated cytometry datasets spanning diverse technologies, including spatial platforms like CODEX. ImmunoPheno complements expert curation and supports continual expansion, providing a scalable framework to enhance the accuracy, reproducibility, and resolution of immunophenotyping.

bioinformatics↗

Ultra-flexible PINE arrays for month-long, continuous intracellular ion flux monitoring in plants with nanomolar accuracy

High-precision in vivo monitoring of ion fluxes is essential yet challenging studying plant electrophysiology such as growth regulation, signal transduction and stress responses. Existing methods for probing ion dynamics are limited by low sensitivity, high invasiveness that interferes physiological processes, and the inability to accurately resolve ion homeostasis with required spatial and temporal resolution. Here, we introduce ultraflexible, plant implantable nanoelectrode (PINE) arrays manufactured on 1.2-m-thick polymer substrates, which enable ultrasensitive and selective measurement of ionic current for month-long via scalable nanofabrication techniques. The fabricated PINE arrays have a smaller dimension than typical plant cells as well as less stiffness, facilitating minimally invasive integration with living plant cells. This subcellular-scale plant-electronic interface allows for reliable, selective detection of K+ flux with a detection limit of [~]10- M, and thus allows continuous, stable monitoring of tomato stem cells over six weeks, capturing dynamic potassium fluctuations during all key growth stages. More importantly, the method permits long-term, real-time tracking of ion-specific dynamics without disrupting plant cellular structure or altering endogenous ion concentrations. Therefore, PINE provides unprecedented access to ion homeostasis and signaling networks, making it an excellent platform for precision agriculture and a foundational tool for future digital plant engineering.

plant biology↗

Optical metabolic imaging of the tricarboxylic acid cycle

The tricarboxylic acid (TCA) cycle lies at the core of cellular metabolism, integrating energy production, biosynthesis and redox homeostasis, yet direct quantitative imaging of its activity in living systems remains challenging. Here we introduce MATRIX-SRS (Metabolic Activity TRacing of the trIcarboXylic acid cycle by Stimulated Raman Scattering microscopy), a platform enabling spatially resolved quantification of TCA-linked metabolism in live cells. Using emerging deuterium-labeled probes, MATRIX-SRS visualizes subcellular TCA-associated carbon-deuterium bonds in live cancer cells and neurons. We then integrate density functional theory, reaction network mapping, and hyperspectral MATRIX-SRS to construct a robust in situ metabolic quantification pipeline. Integrating MATRIX-SRS with isotope-tracing mass spectrometry, we reveal a global attenuation of TCA activity during epithelial-to-mesenchymal transition, providing deep molecular insights. Applying this framework, we further quantify changes in deuterium-labeled biomass in absolute concentrations for the first time, under native and drug-treated conditions, establishing a generalizable foundation for live quantitative spatial metabolomics.

biochemistry↗

Functional In-Context Learning in Genomic Language Models with Nucleotide-Level Supervision and Genome Compression

AO_SCPLOWBSTRACTC_SCPLOWGenomic foundation models aim to learn general-purpose representations directly from DNA sequence, enabling sequence understanding, generation, and probabilistic reasoning across a wide range of biological tasks. Scaling such models to genomic lengths, however, remains challenging due to the tension between long-range context, nucleotide-level resolution, and practical computational efficiency. Architectural innovations have enabled increasingly long nominal inputs, but often struggle to translate additional context into meaningful performance gains, particularly in the presence of sparse functional signal along eukaryotic genomes. In this work, we revisit the design of long-context genomic foundation models from the perspective of training objective and data construction. We introduce Factorized Nucleotide Supervision (FNS), which reconciles efficient k-mer tokenization with single-nucleotide likelihoods through probability marginalization, and Genome Compression Pretraining (GCP), which reshapes the training distribution by concentrating on gene-centric and regulatory regions. Together, these techniques enable standard transformer-based models to perform functional in-context learning without sacrificing nucleotide-level fidelity or computational efficiency. Building on these ideas, we present a family of autoregressive genomic foundation models supporting contexts of up to 98k base pairs across eukaryotic and prokaryotic genomes. Across training-free evaluations and downstream fine-tuning benchmarks, our models consistently improve over prior approaches and match or exceed state-of-the-art baselines while enabling substantially more efficient inference. Together, these results demonstrate that aligning supervision and data regimes with the biological structure of genomic sequence provides a principled and effective path toward scalable and biologically faithful genomic language modeling. Models, data, and scripts for downstream analyses are publicly available at https://huggingface.co/GenerTeam.

genomics↗

A brain dynamic model based on graph neural network reflect the inter-region interaction of cortical areas

A central objective in neuroscience is to elucidate how the brain generates complex dynamic activity through the interactions of brain areas. In this study, we utilized Interaction Network, a graph neural network model, to develop a computational framework for predicting whole-brain cortical blood oxygenation level dependent (BOLD) signals. We derived an Inter-Regional Interaction (IRI) metric to quantify information exchange among brain areas probing the underlying dynamical mechanisms. In addition, the total IRI emitted from each brain region was calculated and defined as the IRI sent by region (RS-IRI). Our model predicted the following 10 time points BOLD activity from initial BOLD signals, and achieved a mean absolute error of 0.04. The predicted functional connectivity (FC) achieves a correlation coefficient of 0.97 compared to the empirical FC. The fluctuation amplitude of the IRI increases with the length of the connection and the largest RS-IRI oscillation amplitude is observed in visual areas. The RS-IRI demonstrates a hierarchical organization, characterized by more concentrated distributions in association regions and larger fluctuation amplitudes in unimodal regions. Applying our approach to Alzheimers disease (AD), we demonstrate that the frequency-specific amplitudes of IRI oscillations discriminate AD patients from healthy controls and correlate with Mini-Mental State Examination scores. Together, this work presents a deep learning-based framework for modeling brain dynamics as well a quantitative index of inter-areal interactions, and offers a new perspective for disease characterization. Author SummaryThe human brain comprises distinct regions that interact through complex fiber tracts, forming the functional dynamics for diverse cognitive processes. We employed fMRI to assess functional activity and DTI to reconstruct fiber tract connectivity. To elucidate how brain function emerges from these inter-regional interactions, we developed a novel computational framework based on Graph Neural Network (GNN) to model the brains interactive dynamics for its capacity to uncover hidden and intricate patterns within data. From this model, we derived a quantitative metric termed Inter-Regional Interaction (IRI), which characterized the fine-grained, dynamic fluctuations in communication between brain areas. Our results suggest that this GNN-based model can accurately simulate brain functional activity and provide a quantitative description of neural interaction patterns. Applying this model to a cohort of Alzheimers disease patients, we demonstrated that the IRI metric not only effectively distinguished patients from healthy controls but also significantly correlated with clinical cognitive performance (MMSE scores). This approach advances our understanding of the fundamental principles of brain function and offers a promising tool for identifying the underlying mechanisms of neurological disorders.

neuroscience↗

The amplitude and latency of the earliest signal in V1 encode bottom-up saliency by feature conjunction

The neural origin of bottom-up saliency for exogenous attention remains highly controversial. In this study, we investigated whether the earliest activity in the primary visual cortex (V1) encodes saliency signals defined by the eye-of-origin and feature-conjunction information. Electroencephalography (EEG) recordings from the human occipital cortex revealed early responses to eye-of-origin (E) and/or orientation (O) singletons, with larger response amplitudes to the double-feature (EO) singletons. The short onset latency (58-70 ms) and polarity reversal of the responses indicate a V1 origin. Importantly, the latency and amplitude of these responses predicted behavioral detection performance. Together, these findings suggest that the timing and amplitude of the earliest signals in V1 represent the saliency of combined feature contrasts for bottom-up attention. These signals unlikely originate from projections of other proposed source areas of saliency, due to the scarcity of necessary monocular neurons to process eye-of-origin information. HighlightsO_LIEye-of-origin information, invisible to the SC, elicits an early saliency signal in V1 within 50-100 ms. C_LIO_LICombined feature contrast enhances V1 saliency responses in a nonlinear fashion. C_LIO_LIThe latency and amplitude of V1 saliency responses predict behavioral detection performance. C_LI

neuroscience↗

Joint Segmental Duplication Co-option Drives Human-specific Transcriptional Readthrough and Expression Fine-tuning of NPEPPS-TBC1D3

Segmental duplication (SD) is a major driver of functional changes in evolution and disease. Many genes embedded within SDs, such as NPEPPS and TBC1D3, display substantial copy number variation (CNV) across individuals. Yet, the precise identification of the functional copies and their transcriptional outputs remains largely unstudied. Focusing on NPEPPS and TBC1D3, we illustrate human-specific expression fine-tuning mechanisms associated with readthrough transcripts. We identified a human-specific NPEPPS-TBC1D3 digenic genomic structure that originated from a joint SD pair and became fixed across populations. Experiments demonstrate that this structure generates NPEPPS-TBC1D3 readthrough transcripts, which are the predominant isoforms of TBC1D3 expression in various cell types, fine-tuning its protein level. Furthermore, a human-specific hypomethylation signal within an upstream CpG island of NPEPPS precisely pinpoints the expressed TBC1D3 paralog. Moreover, we reveal transcriptional readthrough events are [~]3-fold enriched for joint-SD-associated transcriptional readthrough (JSDTR) and identify 109 JSDTR gene pairs, including neurodevelopmentally important pairs and clinically interesting SERF1A/B-SMN1/2. Taken together, our findings comprehensively describe an example of how a joint SD event shaped evolution and suggest that JSDTR is a broad mechanism for the emergence of new functions.

genetics↗