Published August 7, 2025 | Version v1
Poster Open

AI modelling of protein structures can distinguish between sensor and helper NLR immune receptors

  • 1. ROR icon Sainsbury Laboratory
  • 2. ROR icon Rijk Zwaan (Netherlands)
  • 3. ROR icon Imperial College London
  • 4. Kyoto University
  • 5. ROR icon Iwate Biotechnology Research Center

Description

NLR proteins are intracellular immune receptors present across all kingdoms of life, with exceptional diversification in plants. NLRs can function in diverse configurations, including singletons, pairs, and intricate hierarchical networks, to effectively recognize and combat invading threats¹. In NLR pairs and networks, sensor NLRs detect pathogen secreted effectors but require helper NLRs for immune signaling. Upon activation, singleton and helper NLRs oligomerize, insert into the plasma membrane, and act as calcium channels. Here, we propose that the AI system AlphaFold 3 can classify NLR pairs and networks proteins into sensor or helper categories based on predicted structural characteristics. Helper NLRs showed higher AlphaFold 3 confidence scores than sensors when modeled in oligomeric configurations. Furthermore, we could predict funnel-shaped structures—essential for activating immune responses—in helpers but not in sensors. These approaches could overcome the limitations of sequence-based annotation methods and provide new insights into the structural and functional organization of immune receptors.

Files

NP_NGS_v1.pdf

Files (34.0 MB)

Name Size Download all
md5:5ac3347fae21fc66ac5a2affbe98bf8d
10.2 MB Preview Download
md5:757a4b9098c9f90ab204b2dc4d28d8e3
23.8 MB Preview Download

Additional details

Related works

Is described by
Publication: 10.1111/nph.70391 (DOI)
Preprint: 10.1101/2025.02.25.639832 (DOI)

References

  • Contreras et al., 2023, PMID: 37602936
  • Toghani et al., 2024, Zenodo
  • Contreras et al., 2023, PMID: 36579501
  • Toghani et al., 2024, bioRxiv
  • Białas et al., 2018, PMID: 29144205
  • Brabham et., 2018, bioRxiv
  • Pai et al., 2025, bioRxiv