Abstract
Incorporation of unnatural amino acids and peptidomimetic residues into therapeutic peptides is highly efficacious and commonly employed, but generally requires laborious trial-and-error approaches. Previously, we demonstrated that C20 peptide has the potential to be a potential antiviral agent. Herein we report our attempt to improve the biological properties of this peptide by introducing peptidomimetics. Through combined alanine, proline, and sarcosine scans coupled with a competitive fluorescence polarization assay developed for identifying antiviral peptides, we enabled to pinpoint peptoid-tolerant peptide residues within C20 peptide. The synergistic benefits of combining these (and other) commonly employed methods could lead to a easily applicable strategy for designing and refining therapeutically-attractive peptidomimetics. © 2013 Park et al.
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CITATION STYLE
Park, M., Wetzler, M., Jardetzky, T. S., & Barron, A. E. (2013). A Readily Applicable Strategy to Convert Peptides to Peptoid-based Therapeutics. PLoS ONE, 8(3). https://doi.org/10.1371/journal.pone.0058874
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