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Unconventional Secondary Structure Mimics: Ladder-Rungs.

Chen-Ming LinMaritess ArancilloJonathan WhisenantKevin Burgess
Published in: Angewandte Chemie (International ed. in English) (2020)
Secondary structures tend to be recognizable because they have repeating structural motifs, but mimicry of these does not have to follow such well-defined patterns. Bioinformatics studies to match side-chain orientations of a novel hydantoin triazole chemotype (1) to protein-protein interfaces revealed it tends to align well across parallel and antiparallel sheets, like rungs on a ladder. One set of these overlays was observed for the protein-protein interaction uPA⋅uPAR. Consequently, chemotype 1 was made with appropriate side-chains to mimic uPA at this interface. Biophysical assays indicate these compounds did in fact bind uPAR, and elicit cellular responses that affected invasion, migration, and wound healing.
Keyphrases
  • protein protein
  • small molecule
  • wound healing
  • high resolution
  • cell migration
  • single cell
  • case control
  • mass spectrometry