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Greenig, M.

Publications and source records attributed to Greenig, M..

6 recordsLinked to original sources

BioML-bench: Evaluation of AI Agents for End-to-End Biomedical ML

Large language model (LLM) agents hold promise for accelerating biomedical research and development (R&D). Several biomedical agents have recently been proposed, but their evaluation has largely been restricted to question answering (e.g., LAB-Bench) or narrow bioinformatics tasks. Presently, there remains a lack of benchmarks evaluating agent capability in multi-step data analysis workflows or in solving the machine learning (ML) challenges central to AI-driven therapeutics development, such as perturbation response modeling or drug toxicity prediction. We introduce BioML-bench, the first benchmarking suite for evaluating AI agents on end-to-end biomedical ML tasks. BioML-bench spans four domains (protein engineering, single-cell omics, biomedical imaging, and drug discovery) with tasks that require agents to parse a task description, build a pipeline, implement models, and submit predictions graded by established metrics (e.g., AUROC, Spearman). We evaluate four open-source agents: two biomedical specialists (STELLA, Biomni) and two generalists (AIDE, MLAgentBench). On average, agents underperform relative to human baselines, and biomedical specialization does not confer a consistent advantage. We also found that agents which employed more diverse ML strategies more often tended to score highest, suggesting that architecture and scaffolding may be stronger determinants of performance. These findings underscore both the potential and current limits of agentic systems for biomedical ML, and highlight the need for systematic, reproducible evaluations. BioML-bench is provided open-source at github.com/science-machine/biomlbench.

bioinformatics↗

Development of potent humanized TNFα inhibitory nanobodies for therapeutic applications in TNFα-mediated diseases

Tumor necrosis factor-alpha (TNF) is a key pro-inflammatory cytokine implicated in the pathogenesis of numerous inflammatory and autoimmune diseases, including rheumatoid arthritis, inflammatory bowel disease, and neurodegenerative disorders such as Alzheimers Disease. Effective inhibition of TNF is essential for mitigating disease progression and improving patient outcomes. In this study, we present the development and comprehensive characterization of potent humanized TNF inhibitory nanobodies (TNFINbs) derived from camelid single-domain antibodies. In silico analysis of the original camelid nanobodies revealed low immunogenicity, which was further reduced through machine-learning-guided humanization and developability optimization. The two humanized TNFI-Nb variants we developed demonstrated exceptional anti-TNF activity, achieving IC50 values in the picomolar range. Binding assays confirmed their high affinity for TNF, underscoring robust neutralization capabilities. These TNFI-Nbs present valid alternatives to conventional monoclonal antibodies currently used in human therapy, offering potential advantages in potency, specificity, and reduced immunogenicity. Our findings establish a solid foundation for further preclinical development and clinical translation of TNF-targeted nanobody therapies in TNF-mediated diseases.

biochemistry↗

Highly potent novel multi-armoured IL13Rα2 CAR-T subverts the immunosuppressive microenvironment of Glioblastoma

Glioblastoma remains one of the most challenging and lethal brain cancers, with limited treatment options. While CAR-T cells have shown promise in some patients, sustaining T-cell activity and overcoming the immunosuppressive tumour microenvironment remain significant hurdles. Here, we present an armoured CAR-T cell design to address these challenges and enhance persistence in GBM tumours. We developed a highly specific humanised single-domain antibody targeting IL13R2 and included it alongside four additional modular elements in a single retroviral vector for CAR-T generation. Our results demonstrate that this single-cassette CAR-T cell design possesses high resilience against TGF-{beta}-mediated immunosuppression, enhanced tumour-killing capacity through IL-12 secretion while maintaining a favourable safety profile, extended persistence in the host, and an additional layer of safety control through the incorporation of a suicide switch. Importantly, despite its complexity, the construct can still be manufactured efficiently. These advancements represent a significant step forward in addressing key challenges associated with CAR-T cell therapy in solid tumours.

cancer biology↗

Protein Sequence Modelling with Bayesian Flow Networks

Exploring the vast and largely uncharted territory of amino acid sequences is crucial for understanding complex protein functions and the engineering of novel therapeutic proteins. Whilst generative machine learning has advanced protein sequence modelling, no existing approach is proficient for both unconditional and conditional generation. In this work, we propose that Bayesian Flow Networks (BFNs), a recently introduced framework for generative modelling, can address these challenges. We present ProtBFN, a 650M parameter model trained on protein sequences curated from UniProtKB, which generates natural-like, diverse, structurally coherent, and novel protein sequences, significantly outperforming leading autoregressive and discrete diffusion models. Further, we fine-tune ProtBFN on heavy chains from the Observed Antibody Space (OAS) to obtain an antibody-specific model, AbBFN, which we use to evaluate zero-shot conditional generation capabilities. AbBFN is found to be competitive with, or better than, antibody-specific BERT-style models, when applied to predicting individual framework or complimentary determining regions (CDR).

bioinformatics↗

A single-cell transposable element atlas of human cell identity

Single cell RNA sequencing (scRNA-seq) is revolutionizing the study of complex biological systems. However, most sequencing studies overlook the contribution of transposable element (TE) expression to the transcriptome. In both scRNA-seq and bulk tissue RNA sequencing (RNA-seq), quantification of TE expression is challenging due to repetitive sequence content and poorly characterized TE gene models. Here, we developed a tool and analysis pipeline for Single cell Transposable Element Locus Level Analysis of scRNA Sequencing (Stellarscope) that reassigns multi-mapped reads to specific genomic loci using an expectation-maximization algorithm. Using Stellarscope, we built an atlas of TE expression in human PBMCs. We found that locus-specific TEs delineate cell types and define new cell subsets not identified by standard mRNA expression profiles. Altogether, this study provides comprehensive insights into the influence of transposable elements in human biology.

genomics↗

AbNatiV: VQ-VAE-based assessment of antibody and nanobody nativeness for engineering, selection, and computational design

Monoclonal antibodies have emerged as key therapeutics, and nanobodies are rapidly gaining momentum following the approval of the first nanobody drug in 2019. Nonetheless, the development of these biologics as therapeutics remains a challenge. Despite the availability of established in vitro directed evolution technologies that are relatively fast and cheap to deploy, the gold standard for generating therapeutic antibodies remains discovery from animal immunization or patients. Immune-system derived antibodies tend to have favourable properties in vivo, including long half-life, low reactivity with self-antigens, and low toxicity. Here, we present AbNatiV, a deep-learning tool for assessing the nativeness of antibodies and nanobodies, i.e., their likelihood of belonging to the distribution of immune-system derived human antibodies or camelid nanobodies. AbNatiV is a multi-purpose tool that accurately predicts the nativeness of Fv sequences from any source, including synthetic libraries and computational design. It provides an interpretable score that predicts the likelihood of immunogenicity, and a residue-level profile that can guide the engineering of antibodies and nanobodies indistinguishable from immune-system-derived ones. We further introduce an automated humanisation pipeline, which we applied to two nanobodies. Wet-lab experiments show that AbNatiV-humanized nanobodies retain binding and stability at par or better than their wild type, unlike nanobodies humanised relying on conventional structural and residue-frequency analysis. We make AbNatiV available as downloadable software and as a webserver.

bioengineering↗