Combining AI Structure Prediction and Integrative Modeling for Nanobody-Antigen Complexes.

Authors

Miguel Sánchez-Marín, Marco Giulini, Alexandre M J J Bonvin

Published in

Journal of chemical information and modeling. Volume 66. Issue 17. Pages 11445-11458. Sep 14, 2026.

Abstract

Nanobodies exhibit antigen-binding affinities of the same order as those of antibodies, which, along with their small size and unique structural characteristics, makes them well-suited for therapeutic and diagnostic applications. The lack of coevolutionary signals in nanobody-antigen complexes, together with the broad complementarity determining region 3 loop (CDR3) conformational space, poses a challenge for predicting the 3D structure of those complexes with computational modeling and artificial intelligence-based methods. In this context, physics-based information-driven docking can provide an alternative solution. This study evaluates the state-of-the-art machine-learning-based methods for nanobody structure prediction and benchmarks various HADDOCK workflows to model their interaction with antigens using different input nanobody ensembles and information scenarios. We propose an ensemble docking pipeline that achieves high success rates starting from nanobody structural models predicted by AlphaFold2 and ImmuneBuilder. Provided that some information on the epitope is available, our pipeline achieves higher success rates than the AlphaFold baseline on all generated models.

PMID:
42734515
Bibliographic data and abstract were imported from PubMed on 14 Sep 2026.

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