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Streamlined Protein-Protein Interface Loop Mimicry
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DOI：10.1002/anie.202307092.png)
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Abstract
En 中文
Cyclic peptides comprising endocyclic organic fragments, cyclo-organopeptides, can be probes for perturbing protein-protein interactions (PPIs). Finding loop mimics is difficult because of high conformational variability amongst targets. Backbone Matching (BM), introduced here, helps solve this problem in the illustrative cases by facilitating efficient evaluation of virtual cyclo-organopeptide core-structure libraries. Thus, 86 rigid organic fragments were selected to build a library of 602 cyclo-organopeptides comprising Ala and organic parts: cyclo-{-(Ala)n-organo-}. The central hypothesis is hit library members have accessible low energy conformers corresponding to backbone structures of target protein loops, while library members which cannot attain this conformation are probably unworthy of further evaluation. BM thereby prioritizes candidate loop mimics, so that less than 10 cyclo-organopeptides are needed to be prepared to find leads for two illustrative PPIs: iNOS & sdot; SPSB2, and uPA & sdot; uPAR. Backbone Matching (BM) evaluates virtual libraries of cyclic peptidomimetics containing an organic fragment, for interface loop mimicry in protein-protein interactions. It does so by comparing their backbone conformers with interface loops on the protein ligand. Hits for iNOS & sdot; SPSB2 and uPA & sdot; uPAR were validated experimentally.image
Keywords:
Loop Mimicry
Macrocycles
Protein-Protein Interactions
Virtual Screening
Journal
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16.9
Papers:
5.7W
Citations:
53.0W
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Cited Papers
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