Interpreting chemical crosslinks: Score-based approaches and deep neural networks
Chemical cross-linking coupled with mass spectrometry (XL-MS) has become a powerful tool for probing residue-level proximities within macromolecular assemblies. By providing sparse but informative distance restraints, XL-MS can be integrated with electron microscopy and domain-level high-resolution structures to model the architecture of protein complexes. Unlike X-ray crystallography, electron microscopy, or solid-state Nuclear Magnetic Resonance (NMR), XL-MS can be applied under near-physiological conditions, scaled to large modular systems, and performed at higher throughput. In this review, we highlight recent advances in the field, with particular emphasis on the impact of AI-driven structure prediction. As an illustration, we describe a hybrid protocol that combines the Integrative Modeling Platform (IMP) with the deep neural network Chai-1 to dock and refine the helicase Dbp10 on a transient ribosome biogenesis intermediate using XL-MS restraints.
Authors
- Riccardo Pellarin
- Florian Stengel (ORCID: https://orcid.org/0000-0003-1447-4509)
- Jan P. Erzberger (ORCID: https://orcid.org/0000-0002-0266-8835)
- Kai Steffen Stroh (ORCID: https://orcid.org/0000-0001-5239-7124)
- Xingyu Chen
Institutions
- Université Claude Bernard Lyon 1 (FR)
- École Normale Supérieure de Lyon (FR)
- Centre National de la Recherche Scientifique (FR)
- Inserm (FR)
- University of Konstanz (DE)
- Southwestern Medical Center (US)
- The University of Texas Southwestern Medical Center (US)
Publication Details
- Journal
- Current Opinion in Structural Biology
- Published
- 2026-03-02
- DOI
- https://doi.org/10.1016/j.sbi.2026.103237
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00