Biology subjects

Cardente, N.

Publications and source records attributed to Cardente, N..

3 recordsLinked to original sources

bioRxiv2026

MS-BCR-DB: an integrated BCR repertoire database to mine humoral multiple sclerosis signatures

Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system (CNS) in which B cells play a critical role. While B-cell receptor (BCR) sequencing studies in MS are increasing, progress in understanding MS-associated BCR repertoire features and convergent patterns across patients has been limited by small cohorts, heterogeneous experimental methodologies, and fragmented data storage. To overcome these challenges, we developed the MS-BCR-Database, the first publicly accessible and uniformly processed collection of human MS BCR sequencing datasets. We harmonized raw BCR-sequencing data into an AIRR-compliant database incorporating clinical and technical metadata, enabling coherent cross-study analyses. Using this resource, we identified putative disease-associated BCR-sequence features, including CNS-biased V-gene usage, marked oligoclonal expansion in cerebrospinal fluid, and convergent clonotype clusters shared exclusively among MS patients. Integration with antigen-annotated BCR databases revealed matches to antibodies recognizing both viral antigens, including Epstein-Barr virus, and CNS self-proteins. The MS-BCR-Database provides a scalable foundation for mechanistic discovery and biomarker development in MS, while establishing a broadly applicable resource for integrative analyses of BCR repertoires.

bioinformatics↗

bioRxiv2025

Quantitative mapping of antigen specificity in adaptive immune repertoire embedding spaces

The adaptive immune receptor repertoire (AIRR) encompasses an immense diversity of antibody and T-cell receptor sequences, whose collective organization - how receptors are distributed, clustered, and interrelated across sequence and functional (e.g., antigen-binding) dimensions - remains poorly characterized. Representing AIRRs in continuous representation spaces that capture sequence, biochemical, and structural similarity between receptors may enable comparisons beyond discrete sequence features. Using both one-hot encodings and protein language model (PLM) embeddings, we developed a quantitative framework to map immune receptor organization at global (sequence-set-level) and local (single-sequence-level) scales. Applying the geometry-aware Wasserstein-2 distance, we show that the global structure of the AIRR space can be recovered from as few as [~]105 sequence embeddings, at least 10 orders of magnitude smaller than the theoretical immune receptor diversity. We found that immune receptor sequences annotated with different antigen specificities occupy distinct regions of representation space. To resolve local relationships, we introduce a spatial homogeneity metric that quantifies the extent of functional clustering. We found higher spatial homogeneity in embedding spaces than in sequence space for diverse antigen-specific datasets. Our framework establishes a foundation for quantitative mapping of adaptive immune repertoire organization.

immunology↗

bioRxiv2025

PEPE: Scalable extraction of multi-modal protein language model representations

MotivationProtein language models (PLMs) capture intricate amino-acid dependencies, producing embeddings that encode rich structural, functional, and evolutionary information. Despite their potential, current extraction workflows rely on arbitrary choices, with respect to embedding layer, pooling, and padding, that frequently yield suboptimal representations for feature extraction and downstream analyses. Large-scale embedding generation is further limited by inefficiencies in computation and memory: (i) accumulating all model outputs in memory before writing to disk causes severe bottlenecks, and (ii) repeatedly embedding identical sequences to extract different modes introduces redundant computation and drastically reduces throughput and scalability. ResultsWe introduce PEPE (Parallel Extraction for Protein Embeddings), a command-line tool and Python library that enables efficient, high-throughput, and multimodal extraction from protein language models. PEPEs parallelized and streaming-based architecture achieves runtimes several orders of magnitude faster than sequential approaches. Unlike conventional methods--whose peak memory usage scales linearly with output size and fails when memory capacity is exceeded--PEPE maintains stable, low memory consumption, enabling multimodal embedding extraction even beyond available RAM. PEPE supports a wide range of state-of-the-art and custom PLMs through a simple, flexible interface. By combining scalability, robustness, and ease of use, PEPE allows researchers to generate massive, information-rich embedding datasets efficiently, and facilitate the discovery of optimal representations for structural, functional, and evolutionary downstream tasks. By streamlining the generation of diverse embedding configurations, PEPE provides researchers with the necessary data to identify high-performing latent states for specific biological contexts without requiring additional computational resources. Availability and ImplementationPEPE is a command-line tool written in Python and published under MIT license. The source code and documentation are available at https://github.com/csi-greifflab/pepe-cli. PEPE is also available for installation from PyPI under https://pypi.org/project/pepe-cli and deposited on Zenodo at https://zenodo.org/records/15912054.

bioinformatics↗