Literature DB >> 32176815

Unconventional Secondary Structure Mimics: Ladder-Rungs.

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 uPAuPAR. 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.
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  cancer; peptide; peptidomimetics; protein-protein interactions; uPAR

Mesh:

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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


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