8OYY

De novo designed soluble GPCR-like fold GLF_32

Summary for 8OYY

• Entry DOI: 10.2210/pdb8oyy/pdb
• Descriptor: De novo designed soluble GPCR-like protein, POTASSIUM ION, CHLORIDE ION, ... (4 entities in total)
• Functional Keywords: gpcr, solubilized, de novo designed, de novo protein
• Biological source: synthetic construct
• Total number of polymer chains: 2
• Total formula weight: 55729.20

Authors

Pacesa, M.,Correia, B.E. (deposition date: 2023-05-05, release date: 2023-10-18, Last modification date: 2024-08-14)

Primary citation

Goverde, C.A.,Pacesa, M.,Goldbach, N.,Dornfeld, L.J.,Balbi, P.E.M.,Georgeon, S.,Rosset, S.,Kapoor, S.,Choudhury, J.,Dauparas, J.,Schellhaas, C.,Kozlov, S.,Baker, D.,Ovchinnikov, S.,Vecchio, A.J.,Correia, B.E.
Computational design of soluble and functional membrane protein analogues.
Nature, 631:449-458, 2024

PubMed Abstract: De novo design of complex protein folds using solely computational means remains a substantial challenge. Here we use a robust deep learning pipeline to design complex folds and soluble analogues of integral membrane proteins. Unique membrane topologies, such as those from G-protein-coupled receptors, are not found in the soluble proteome, and we demonstrate that their structural features can be recapitulated in solution. Biophysical analyses demonstrate the high thermal stability of the designs, and experimental structures show remarkable design accuracy. The soluble analogues were functionalized with native structural motifs, as a proof of concept for bringing membrane protein functions to the soluble proteome, potentially enabling new approaches in drug discovery. In summary, we have designed complex protein topologies and enriched them with functionalities from membrane proteins, with high experimental success rates, leading to a de facto expansion of the functional soluble fold space.

PubMed: 38898281
DOI: 10.1038/s41586-024-07601-y

Experimental method

X-RAY DIFFRACTION (1.85 Å)