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Biology subjects

Pereira, L. S.

Publications and source records attributed to Pereira, L. S..

2 recordsLinked to original sources

Bacterial proteome foundation model enhances functional prediction from enzymes to ecological interactions

Bacteria play fundamental roles in ecosystems, human health, and biotechnology. Although bacterial genome sequencing data have accumulated rapidly over the past decade, the metabolic and ecological functions carried out by most sequenced bacteria remain poorly understood, apart from a few well-studied taxa and traits. Establishing a general framework that comprehensively captures the relationship between bacterial genomes and the diverse biological functions they encode remains a major challenge, as it requires embedding individual genes within their broader genomic context and modeling their combined effects across complex biological pathways and networks. The difficulty is further compounded by the limited functional annotations available for most bacterial genomes. Here, we introduce BacPT, a proteome foundation model trained on tens of thousands of complete genomes spanning diverse bacterial taxa. BacPT captures both local and genome-wide information, enabling the generation of contextualized gene embeddings and functionally rich representations of the whole genome. We demonstrate the utility of BacPT across diverse prediction tasks spanning multiple biological scales. BacPT embeddings improve the prediction of enzyme activities, biosynthetic gene clusters, metabolic traits, and ecological interaction outcomes. Our results highlight that unsupervised deep learning applied at the scale of entire proteomes provides a powerful approach for characterizing gene interactions and mapping functional landscapes for bacteria.

genomics↗

The light chain of the L9 antibody is critical for binding circumsporozoite protein minor repeats and preventing malaria

L9 is a potent human monoclonal antibody (mAb) that preferentially binds two adjacent NVDP minor repeats and cross-reacts with NANP major repeats of the Plasmodium falciparum circumsporozoite protein (PfCSP) on malaria-infective sporozoites. Understanding this mAbs ontogeny and mechanisms of binding PfCSP to neutralize sporozoites will facilitate vaccine development. Here, we isolated mAbs clonally related to L9 and showed that this B-cell lineage has baseline NVDP affinity and evolves to acquire NANP reactivity. Pairing the L9 kappa light chain (L9{kappa}) with clonally-related heavy chains resulted in chimeric mAbs that cross-linked two NVDP, cross-reacted with NANP, and more potently neutralized sporozoites compared to their original light chain. Structural analyses revealed that chimeric mAbs bound the minor repeat motif in a type-1 {beta}-turn seen in other repeat-specific antibodies. These data highlight the importance of L9{kappa} in binding NVDP on PfCSP to neutralize SPZ and suggest that PfCSP-based immunogens might be improved by presenting [≥]2 NVDP.

immunology↗