Linear-time prediction of proteome-scale microbial protein interactions

Protein-protein interactions (PPIs) underpin biological function, yet proteome-scale interaction prediction remains bottlenecked by the quadratic computational complexity of all-vs.-all pairwise comparisons. Here, we present FlashPPI, a contrastive learning framework, grounded in residue-level interactions, that enables linear-time prediction of physical protein interfaces across a microbial proteome. By leveraging a genomic language model that captures cross-protein coevolutionary signals from metagenomic sequences, FlashPPI aligns interacting partners in a shared latent space. We demonstrate a four-fold performance increase over existing sequence-based methods, while reducing proteome-wide screening time from days to minutes. Crucially, FlashPPI achieves comparable screening performance to state-of-the-art structure-folding models at a fraction of the computational cost. Finally, we integrate FlashPPI into an interactive web platform that combines predicted networks with functional annotations and genomic context, making proteome-wide network analysis rapid and accessible for microbial discovery.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-06-17
DOI
https://doi.org/10.1073/pnas.2610619123
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
0.00

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article

Linear-time prediction of proteome-scale microbial protein interactions

Yunha Hwang, Nicolo G. Zulaybar, Imane Bouzit, Matt Tranzillo et al.
Proceedings of the National Academy of Sciences
Bioinformatics and Genomic Networks
article

Linear-time prediction of proteome-scale microbial protein interactions

Yunha Hwang, Nicolo G. Zulaybar, Imane Bouzit, Matt Tranzillo, Andre Cornman
article en

Abstract

Protein-protein interactions (PPIs) underpin biological function, yet proteome-scale interaction prediction remains bottlenecked by the quadratic computational complexity of all-vs.-all pairwise comparisons. Here, we present FlashPPI, a contrastive learning framework, grounded in residue-level interactions, that enables linear-time prediction of physical protein interfaces across a microbial proteome. By leveraging a genomic language model that captures cross-protein coevolutionary signals from metagenomic sequences, FlashPPI aligns interacting partners in a shared latent space. We demonstrate a four-fold performance increase over existing sequence-based methods, while reducing proteome-wide screening time from days to minutes. Crucially, FlashPPI achieves comparable screening performance to state-of-the-art structure-folding models at a fraction of the computational cost. Finally, we integrate FlashPPI into an interactive web platform that combines predicted networks with functional annotations and genomic context, making proteome-wide network analysis rapid and accessible for microbial discovery.

Proceedings of the National Academy of SciencesVol. 123(25)
Institute of Computing Technology (CN), Massachusetts Institute of Technology (US)
Schmidt Futures, Gordon and Betty Moore Foundation
Openalex Percentile: Top 11%
Bioinformatics and Genomic Networks
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