Abstract
Supramolecular receptors such as water-soluble calixarenes are in development as ‘molecular glues’ for protein assembly. Here, we obtained cocrystals of sulfonato-calix[6]arene (sclx6) and yeast cytochrome c (cytc) in the presence of imidazole. A crystal structure at 2.65 Å resolution reveals major structural rearrangement and disorder in imidazole-bound cytc. The largest protein-calixarene interface involves 440 Å2 of the protein surface with key contacts at Arg13, Lys73, and Lys79. These lysines participate in alkaline transitions of cytc and are part of Ω-loop D, which is substantially restructured in the complex with sclx6. The structural modification also includes Ω-loop C, which is disordered (residues 41–55 inclusive). These results suggest the possibility of using supramolecular scaffolds to trap partially disordered proteins.
| Original language | English |
|---|---|
| Pages (from-to) | 2112-2117 |
| Number of pages | 6 |
| Journal | FEBS Letters |
| Volume | 593 |
| Issue number | 16 |
| DOIs | |
| Publication status | Published - Aug 2019 |
Keywords
- disordered
- imidazole
- lysine
- omega loop
- supramolecular