Precise assembly of complex beta sheet topologies from de novo designed building blocks
- University of Washington, United States
- Fred Hutchinson Cancer Research Center, United States
- Columbia University, United States
- Rutgers, The State University of New Jersey, United States
Figures
Figure 1
Generation of protein domains with single extended beta sheets by inserting one beta sheet containing protein into another.
(A) Insertion of a ferrrodoxin domain (purple) into TOP7 (red). (B) Insertion of one ferrodoxin domain into another. In both cases, two beta strands from each partner (red and purple) are …
Figure 2 with 1 supplement
Comparison of the crystal structure of ferredoxin-TOP7 fusion to design model.
(A) Backbone superposition of the crystal structure of ferredoxin-TOP7 (4KYZ, chain A) with the design model. The backbones of the two proteins are nearly identical. (B, C) The core sidechain …
Figure 2—figure supplement 1
The circular dichroism spectrum of ferrodoxin-TOP7 has the shape expected for an alpha/beta protein.
https://doi.org/10.7554/eLife.11012.005
Figure 3 with 2 supplements
Comparison of the crystal structure of the ferredoxin-ferredoxin fusion to the design model.
The crystal structure (5CW9) aligns well with the design model over both the helices (A) and the fused beta sheet (B).
Figure 3—figure supplement 1
Circular dichroism spectra of ferrrodoxin-ferrodoxin at 25°C.
https://doi.org/10.7554/eLife.11012.007
Figure 3—figure supplement 2
Ferredoxin-Ferredoxin 2Fo-Fc omit map superimposed with crystal structure shows core packing of host (A) and insert (B) domains.
https://doi.org/10.7554/eLife.11012.008
Figure 4 with 2 supplements
Top two SCOP domain structural homologues for Fd-Top7 (A) and Fd-Fd (B) designed domain found in TM-align searches.
Ribbon diagrams are shown on left, the strand connectivity, at the right. The beta strand connectivity is quite different in the designs than in these closest structural matches.
Figure 4—figure supplement 1
Parent domain PDB structures (2KL8, 1QYS) and daughter designed folds (5CW9,4KYZ) (pink) mapped into the α+β region of the SCOP domains network of Nepomnyachi et al. (A) and zoomed region (B) highlighting parent, designed, and first neighbor folds.
https://doi.org/10.7554/eLife.11012.010
Figure 4—figure supplement 2
Neutral drift mutant models, relative changes to predicted free energy of folding in REU (Rosetta Energy Units), and multiple sequence alignment of parent and designed sequences, showing mutations in ferredoxin-top7 (A) and ferredoxin-ferredoxin (B).
https://doi.org/10.7554/eLife.11012.011Additional files
-
Supplementary file 1
Crystallographic data.
- https://doi.org/10.7554/eLife.11012.012
