Discovery of peptidic miR-21 processing inhibitor by mirror image phage display: A novel method to generate RNA binding D-peptides

[Display omitted] A novel method to generate RNA binding D-peptide has been developed. To achieve the screening method, phage display was applied to “Mirrored” RNA (L-enantiomer of RNA). We have selected pre-miR21 as an initial screening target to demonstrate the method. The mirrored pre-miR-21 bind...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2017-02, Vol.27 (4), p.826-828
Hauptverfasser: Sakamoto, Kotaro, Otake, Kentaro, Umemoto, Tadashi
Format: Artikel
Sprache:eng
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Zusammenfassung:[Display omitted] A novel method to generate RNA binding D-peptide has been developed. To achieve the screening method, phage display was applied to “Mirrored” RNA (L-enantiomer of RNA). We have selected pre-miR21 as an initial screening target to demonstrate the method. The mirrored pre-miR-21 binding peptide sequences were successfully obtained, and were chemically synthesized using D-amino acids. D-peptide is expected to have favorable properties as a drug candidate such as protease resistance and low immunogenicity. As a result of binding evaluation of the D-peptide to pre-miR-21, the EC50 value was 440nM. In addition, the D-peptide possessed inhibition activity to miR-21 processing.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2017.01.023