8BL6
De novo single-chain immunoglobulin dimer scIg12+EF3a
Summary for 8BL6
| Entry DOI | 10.2210/pdb8bl6/pdb |
| Related | 8BL3 |
| Descriptor | dIG14-scdim-EF62, GLYCEROL, TERBIUM(III) ION (3 entities in total) |
| Functional Keywords | de novo, immunoglobulin, single-chain dimer, sandwich, beta, ef-hand, de novo protein |
| Biological source | synthetic construct |
| Total number of polymer chains | 1 |
| Total formula weight | 20710.08 |
| Authors | |
| Primary citation | Roel-Touris, J.,Nadal, M.,Marcos, E. Single-chain dimers from de novo immunoglobulins as robust scaffolds for multiple binding loops. Nat Commun, 14:5939-5939, 2023 Cited by PubMed Abstract: Antibody derivatives have sought to recapitulate the antigen binding properties of antibodies, but with improved biophysical attributes convenient for therapeutic, diagnostic and research applications. However, their success has been limited by the naturally occurring structure of the immunoglobulin dimer displaying hypervariable binding loops, which is hard to modify by traditional engineering approaches. Here, we devise geometrical principles for de novo designing single-chain immunoglobulin dimers, as a tunable two-domain architecture that optimizes biophysical properties through more favorable dimer interfaces. Guided by these principles, we computationally designed protein scaffolds that were hyperstable, structurally accurate and robust for accommodating multiple functional loops, both individually and in combination, as confirmed through biochemical assays and X-ray crystallography. We showcase the modularity of this architecture by deep-learning-based diversification, opening up the possibility for tailoring the number, positioning, and relative orientation of ligand-binding loops targeting one or two distal epitopes. Our results provide a route to custom-design robust protein scaffolds for harboring multiple functional loops. PubMed: 37741853DOI: 10.1038/s41467-023-41717-5 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.8 Å) |
Structure validation
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