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Cited by 276Protein Structure and DynamicsMachine Learning in BioinformaticsComputational Drug Discovery Methods

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ScanNet: an interpretable geometric deep learning model for structure-based protein binding site prediction

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Tubiana, Jérôme, Schneidman-Duhovny, Dina, Wolfson, Haim J.·2022·Nature Methods
DOI 10.1038/s41592-022-01490-7

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Abstract

Predicting the functional sites of a protein from its structure, such as the binding sites of small molecules, other proteins or antibodies, sheds light on its function in vivo. Currently, two classes of methods prevail: machine learning models built on top of handcrafted features and comparative modeling. They are, respectively, limited by the expressivity of the handcrafted features and the availability of similar proteins. Here, we introduce ScanNet, an end-to-end, interpretable geometric deep learning model that learns features directly from 3D structures. ScanNet builds representations of atoms and amino acids based on the spatio-chemical arrangement of their neighbors. We train ScanNet for detecting protein-protein and protein-antibody binding sites, demonstrate its accuracy-including for unseen protein folds-and interpret the filters learned. Finally, we predict epitopes of the SARS-CoV-2 spike protein, validating known antigenic regions and predicting previously uncharacterized ones. Overall, ScanNet is a versatile, powerful and interpretable model suitable for functional site prediction tasks. A webserver for ScanNet is available from http://bioinfo3d.cs.tau.ac.il/ScanNet/ .

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Research works printed but not linked: 14

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Metadata

Authors
Tubiana, J., Schneidman-Duhovny, D., & Wolfson, H. J.
Affiliations
Tel Aviv University (IL)
Corresponding author
  • Tubiana, Jérôme
  • Wolfson, Haim J.
ORCID
Venue
Nature Methods
Publisher
Springer Science and Business Media LLC
Published
2022-05-30
Volume
19
Issue
6
Pages
730-739
ISSN
  • 1548-7091 (ISSN-L)
  • 1548-7105
DOI
10.1038/s41592-022-01490-7
OpenAlex
W4229031603
Cited by
274
References
104
Citations by year
2026: 70 · 2025: 75 · 2024: 69 · 2023: 48 · 2022: 11
FWCI
16.82
Type
journal article
Language
en
Open access
Licence
Locations
  • Nature Methods (publishedVersion)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • Research Square (acceptedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
Human Frontier Science Program (LT001058/2019-C)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Drug Discovery › Computational Drug Discovery Methods
Keywords
protein binding site prediction, geometric deep learning, model interpretability, protein structure, protein-protein binding, epitope prediction, SARS-CoV-2 spike protein
MeSH terms
Deep Learning, COVID-19, SARS-CoV-2, Binding Sites, Humans, Protein Binding, Proteins, Spike Glycoprotein, Coronavirus

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