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Bianchin de Oliveira, G.

Publications and source records attributed to Bianchin de Oliveira, G..

2 recordsLinked to original sources

ProtEnrich: Residual Multimodal Enrichment of Protein Sequence Embeddings

Protein language models effectively capture evolutionary and functional signals from sequence data but lack explicit representation of the biophysical properties that govern protein structure and dynamics. Existing multimodal approaches attempt to integrate such physical information through direct fusion, often requiring multimodal inputs at inference time and distorting the geometry of the sequence embedding space, which can disrupt the semantic organization learned from evolutionary information. Consequently, a fundamental challenge of how to incorporate structural and dynamical knowledge into sequence representations without disrupting their semantic organization, enabling sequence-based models to better capture the biophysical properties governing protein structure and function. We introduce ProtEnrich, a representation learning framework based on a residual multimodal enrichment paradigm. ProtEnrich decomposes sequence embeddings into two complementary latent subspaces, an anchor subspace that preserves sequence semantics, and an alignment subspace that encodes biophysical relationships. By converting multimodal information derived from ProstT5 and RocketSHP to a low-energy residual component, our approach injects physical representation while maintaining the original sequence embedding while preserving their original semantic geometry, avoiding the need for multimodal inputs at inference time. Across eight diverse protein foundational models trained on 550,120 SwissProt proteins with AlphaFold structures, enriched embeddings improved zero-shot remote homology retrieval, increasing Precision@10 and MRR by up to 0.13 and 0.11, respectively. Downstream performance also improved on structure-dependent tasks, reducing fluorescence prediction error by up to 16% and increasing metal ion binding AUCROC by up to 2.4 points, while requiring only sequence input at inference. Source code is available at https://github.com/pcdslab/ProtEnrich, pretrained models and datasets are available at https://huggingface.co/collections/SaeedLab/protenrich.

bioinformatics↗

BindScreen: Protein-Centric Contrastive Learning for Sequence-Based Virtual Screening

Virtual screening ranks candidate molecules against a protein target. Sequence-based deep learning avoids dockings structural requirements, but pair-based models need one forward pass per protein-molecule pair and scale poorly to large libraries. Dual-encoder contrastive models remove that bottleneck, yet standard CLIP training assumes a symmetric, one-to-one correspondence, whereas protein-molecule binding is asymmetric and many-to-many. We present Bind-Screen, a sequence-only dual-encoder screening model, and show that the decisive design choice is not the contrastive loss but how the batch is built. BindScreen combines a protein-centric batch construction and an asymmetric multi-positive InfoNCE loss. A factorial ablation separates the two contributions: the loss alone degrades performance under standard CLIP batching, the protein-centric batch alone recovers most of the gain, and the combination performs best. The effect is encoder-agnostic across eight protein language models spanning four architectural families. By decoupling protein count from molecule count per batch, BindScreen reaches higher validation BEDROC in 86 hours than standard CLIP reaches in 460 hours, and needs about seven times fewer forward passes to screen LIT-PCBA than pair-based models. The source code, pretrained checkpoints, and datasets are publicly available at https://github.com/pcdslab/BindScreen and https://huggingface.co/collections/SaeedLab/bindscreen

bioinformatics↗