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Satani, S.

Publications and source records attributed to Satani, S..

2 recordsLinked to original sources

Systematic functional annotation of thousands of BAHD acyltransferases in plant genomes using Protein Language Model and phylogenomic tools

The functional annotation of plant genes lags significantly behind their genomic annotation. Closing this gap requires thorough cataloging of reported protein activities alongside predictive methods that scale beyond sequence-similarity inference. Focusing on the BAHD acyltransferase enzyme family as a model, we assembled FuncZymeDB-BAHD, a large database of 2,705 LLM-retrieved and curated enzyme-acceptor-donor activities covering 336 BAHDs from 156 plant species, a 2-to-6-fold expansion over Swiss-Prot and prior compilations. We further developed FuncPred-OG, which maps queries to orthologous groups and previously characterized enzymes in FuncZymeDB-BAHD, returning hits with high evidence provenance. FuncPred-OG enabled functional prediction of over half of BAHDs across 85 plant proteomes, of which five novel predictions were validated via in vitro assays and recent studies. For the remaining BAHDs without FuncPred-OG annotation, we developed FuncPred-AI, where logistic-regression classifiers trained on protein language model embeddings achieved high Area-Under-the-Precision-Recall-curve (AUPR) scores and correct-hit rates up to 93%. FuncPred-AI yielded [≥]1 probable donor/acceptor annotation for 99.9% (8894/8897) of BAHDs in our pan-plant dataset. Finally, the FuncPred workflow and datasets were deployed on a web portal for broader utilization, potentially reducing experimentalists efforts for selecting candidates from days to minutes. Overall, this framework provides a generalizable template for functional annotation of entire enzyme families.

bioinformatics↗

Modeling Oncolytic Vaccinia Virus Therapy Highlights Neutrophil Impact on Tumor Suppression

AO_SCPLOWBSTRACTC_SCPLOWOncolytic vaccinia viruses (OVVs) present a promising approach for melanoma treatment due to their ability to selectively infect and lyse tumor cells. In this study, we use an ordinary differential equation (ODE) model of tumor growth inhibited by OVV activity to parameterize previous research on the effect of neutrophil depletion in B16-F10 melanoma tumors in mice. We find that the data are best fit by a model that accounts for neutrophil-mediated viral clearance, and that neutrophil depletion provides a mechanism for enhanced OVV efficacy and tumor reduction. We also find that parameter estimates for the most effective OVV regime share characteristics, most notably a low viral clearance rate by neutrophils, that might explain the improved outcomes. Further studies examining the impact of neutrophil modulation across different tumor models may help elucidate the extent to which these findings generalize and inform the design of novel OVV-based cancer therapies.

cancer biology↗