8UQF
Crystal structure of designed cortisol-binding protein hcy129_mpnn5
Summary for 8UQF
| Entry DOI | 10.2210/pdb8uqf/pdb |
| Descriptor | designed cortisol-binding protein hcy129_mpnn5, (11alpha,14beta)-11,17,21-trihydroxypregn-4-ene-3,20-dione, SULFATE ION, ... (4 entities in total) |
| Functional Keywords | ntf2, cortisol binding, de novo protein |
| Biological source | synthetic construct |
| Total number of polymer chains | 2 |
| Total formula weight | 31633.83 |
| Authors | Pellock, S.J.,Bera, A. (deposition date: 2023-10-23, release date: 2024-11-20, Last modification date: 2026-07-08) |
| Primary citation | Lee, G.R.,Pellock, S.J.,Norn, C.,Tischer, D.,Dauparas, J.,Anishchenko, I.,Mercer, J.A.M.,Kang, A.,Bera, A.K.,Nguyen, H.,Brackenbrough, E.,Sankaran, B.,Goreshnik, I.,Vafeados, D.,Roullier, N.,Han, H.L.,Coventry, B.,Haddox, H.K.,Liu, D.R.,Yeh, A.H.,Baker, D. Small-molecule binding and sensing with a designed protein family. Nat Commun, 17:-, 2026 Cited by PubMed Abstract: The de novo design of small-molecule-binding proteins holds great promise as a potential tool to develop sensors on-demand for arbitrary small molecules. Here we combine deep learning and physics-based methods to generate a family of proteins with diverse and designable pocket geometries, which we employ to computationally design binders for six small-molecule targets. Biophysical characterization of the designed binders reveals nanomolar to low micromolar binding affinities and atomic-level design accuracy. Additionally, we use a cortisol binder to design a chemically induced dimerization (CID) system that enables the construction of a biosensor for cortisol detection. The approach described here demonstrates the potential of the NTF2 fold and deep learning-based protein design in sensor development, paving the way for future platforms to design binders and sensors for small molecules across analytical, environmental, and biomedical applications. PubMed: 41904144DOI: 10.1038/s41467-026-70953-8 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.52 Å) |
Structure validation
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