Modular repeat protein sculpting using rigid helical junctions
By T. Brunette, M. J. Bick, J. Hansen, C. Chow, J. Kollman, David Baker. 2020
42 citations recorded by the source corpus.
Significance The ability to robustly control macromolecular shape on the nanometer length scale is important for a wide range of biomedical and materials applications. DNA nanotechnology has achieved considerable success in building up complex structures from a small number of types of building blocks. We describe a large library of protein building blocks and junctions between them that enable the design of proteins with a wide range of shapes through modular combination of blocks rather than traditional and more complex design at the level of amino acid residues. The ability to precisely design large proteins with diverse shapes would enable applications ranging from the design of protein binders that wrap around their target to the positioning of multiple functional sites in specified orientations. We describe a protein backbone design method for generating a wide range of rigid fusions between helix-containing proteins and use it to design 75,000 structurally unique junctions between monomeric and homo-oligomeric de novo designed and ankyrin repeat proteins (RPs). Of the junction designs that were experimentally characterized, 82% have circular dichroism and solution small-angle X-ray scattering profiles consistent with the design models and are stable at 95 °C. Crystal structures of four designed junctions were in close agreement with the design models with rmsds ranging from 0.9 to 1.6 Å. Electron microscopic images of extended tetrameric structures and ∼10-nm-diameter “L” and “V” shapes generated using the junctions are close to the design models, demonstrating the control the rigid junctions provide for protein shape sculpting over multiple nanometer length scales.
Subfields: Ecology, Molecular Biology
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In Ecology
In Molecular Biology
- David Baker
- Xingjie Pan
- Sergey Ovchinnikov
- Tanja Kortemme
- David E. Kim
- Ivan V. Anishchenko
- Yang Zhang
- Jeffrey J. Gray
Citations in the corpus
- Protein sequence design by conformational landscape optimization (2021, background): “S11): LayerDesign, which disallows amino acids based on their surface exposure (21), and fragment-based PSSMs, which favor local sequence–structure relationships (22).”
- Recent advances in de novo protein design: Principles, methods, and applications (2021, background): “A large number of proteins with diverse shapes can be generated by designing rigid junctions to connect helical repeat proteins (69).”
- Reconfigurable asymmetric protein assemblies through implicit negative design (2021, unknown): “1E) ( 23 ).”