Calixarene capture of partially unfolded cytochrome c

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15 Citations (Scopus)

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 languageEnglish
Pages (from-to)2112-2117
Number of pages6
JournalFEBS Letters
Volume593
Issue number16
DOIs
Publication statusPublished - Aug 2019

Keywords

  • disordered
  • imidazole
  • lysine
  • omega loop
  • supramolecular

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