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Unconventional Secondary Structure Mimics: Ladder‐Rungs
Author(s) -
Lin ChenMing,
Arancillo Maritess,
Whisenant Jonathan,
Burgess Kevin
Publication year - 2020
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202002639
Subject(s) - antiparallel (mathematics) , chemotype , chemistry , protein secondary structure , urokinase receptor , oligopeptide , stereochemistry , structural motif , biophysics , peptide , biochemistry , biology , receptor , physics , chromatography , quantum mechanics , magnetic field , essential oil
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.