| Literature DB >> 32176815 |
Chen-Ming Lin1, Maritess Arancillo1, Jonathan Whisenant1, Kevin Burgess1.
Abstract
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.Entities:
Keywords: cancer; peptide; peptidomimetics; protein-protein interactions; uPAR
Mesh:
Substances:
Year: 2020 PMID: 32176815 PMCID: PMC7717619 DOI: 10.1002/anie.202002639
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336