Quantitative machine learning of protein interactions reveals the multiscale organization and molecular syntax of signaling networks
- 1Columbia University
Abstract
Cells employ dense networks of transient protein-protein interactions mediated by modular peptide-binding domains and unstructured peptidic motifs for high-fidelity information processing. How these networks physically execute computations through protein interactions governed by complex intra- and intermolecular mechanisms remains indiscernible from current, sparse and non-quantitative, maps of the human interactome. Here, we introduce a quantitative statistical mechanical modeling (QSM) approach for machine learning domain-peptide affinities with experimental-level accuracy. Leveraging a new, principled algorithm for data harmonization and a biophysically informed neural network architecture, QSM learns to predict dissociation constants directly from amino acid sequences with calibrated confidence. We use QSM to construct the first quantitative drafts of human signaling networks and study these networks across three physical scales--recognition mechanisms of modular binding domains, combinatorial logic of multi-dentate proteins, and pathways inferred from de novo inference of protein interaction networks. We find that (i) modular domains, based on their binding preferences, selectivities, and strengths, fall into a limited number of biophysical equivalence groups, (ii) those domains, along with peptidic motifs, are "syntactically" combined within proteins to yield multivalent recognition mechanisms, and (iii) the organization of cellular function can be traced back to algorithmically detectable modules induced by domain-mediated interactions. In aggregate, these analyses instantiate a tractable roadmap towards a comprehensive, mechanistic, and simulatable articulation of the systems biology of signaling.
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BibTeX
@misc{rogers2026quantitative,
title = {{Quantitative machine learning of protein interactions reveals the multiscale organization and molecular syntax of signaling networks}},
author = {J. R. Rogers and L. P. Cardani and N. H. Shah and M. AlQuraishi},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.25.754499},
url = {https://www.biorxiv.org/content/10.64898/2026.09.25.754499v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Quantitative machine learning of protein interactions reveals the multiscale organization and molecular syntax of signaling networks
AU - J. R. Rogers
AU - L. P. Cardani
AU - N. H. Shah
AU - M. AlQuraishi
PY - 2026
DA - 2026/09/25
PB - bioRxiv
DO - 10.64898/2026.09.25.754499
UR - https://www.biorxiv.org/content/10.64898/2026.09.25.754499v1
AB - Cells employ dense networks of transient protein-protein interactions mediated by modular peptide-binding domains and unstructured peptidic motifs for high-fidelity information processing. How these networks physically execute computations through protein interactions governed by complex intra- and intermolecular mechanisms remains indiscernible from current, sparse and non-quantitative, maps of the human interactome. Here, we introduce a quantitative statistical mechanical modeling (QSM) approach for machine learning domain-peptide affinities with experimental-level accuracy. Leveraging a new, principled algorithm for data harmonization and a biophysically informed neural network architecture, QSM learns to predict dissociation constants directly from amino acid sequences with calibrated confidence. We use QSM to construct the first quantitative drafts of human signaling networks and study these networks across three physical scales--recognition mechanisms of modular binding domains, combinatorial logic of multi-dentate proteins, and pathways inferred from de novo inference of protein interaction networks. We find that (i) modular domains, based on their binding preferences, selectivities, and strengths, fall into a limited number of biophysical equivalence groups, (ii) those domains, along with peptidic motifs, are "syntactically" combined within proteins to yield multivalent recognition mechanisms, and (iii) the organization of cellular function can be traced back to algorithmically detectable modules induced by domain-mediated interactions. In aggregate, these analyses instantiate a tractable roadmap towards a comprehensive, mechanistic, and simulatable articulation of the systems biology of signaling.
ER -