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Biology subjects

Rumbelow, J.

Publications and source records attributed to Rumbelow, J..

2 recordsLinked to original sources

Growth Cost and Transport Efficiency Tradeoffs Define Root System Optimization Across Varying Developmental Stages and Environments in Arabidopsis

Root system architecture (RSA) is central to plant adaptation and fitness, yet the design principles and regulatory mechanisms connecting RSA to environmental adaptation are not well understood. We developed Ariadne, a semi-automated software for quantifying cost-efficiency tradeoffs of RSA by mapping root networks onto a Pareto-optimality framework, which describes the balance between resource transport efficiency and construction cost. Applying Ariadne to Arabidopsis thaliana, we found that root architectures consistently assume Pareto-optimal forms across developmental stages, genotypes, and environmental conditions. Using the Discovery Engine, an engine that combines machine learning together with interpretability techniques, we found developmental stage, the hy5/chl1-5 genotype, and manganese availability as important determinants of the cost-efficiency tradeoff, with manganese exerting a unique influence not observed for other nutrients. These results reveal that RSA plasticity is genetically constrained to cost-efficiency optimal configurations and that developmental and environmental factors shift RSA on the pareto front, with manganese acting as a strong modulator of the transport efficiency and construction cost balance.

plant biology↗

Automated Discovery of Patterns in T-Cell Receptor Physicochemical Signatures

Accurately distinguishing antigen-reactive from non-reactive T-cell receptors (TCRs) is critical for advancing TCR-based immunotherapies and vaccines. Predicting antigen reactivity from physicochemical properties of the TCR sequence alone could enable rapid, low-cost identification of TCRs of interest, accelerating therapeutic discovery. In this paper, we use the Discovery Engine, a novel system for automated knowledge discovery from data, to classify published tumour antigen-reactive and non-reactive TCRs collected from cancer patients. Beyond classification, the Discovery Engine extracts interpretable combinatorial patterns (e.g., combinations of CDR3 length, net charge, and hydrophobicity) that predict whether a TCR is antigen-reactive. These patterns point to biologically meaningful features linked to tumour antigen recognition and could inform rational TCR design and prioritization. Notably, over half of the predictive patterns involve features from both the alpha and beta chains, highlighting the importance of considering both in assessing antigen specificity.

bioinformatics↗