| Literature DB >> 26663660 |
Oleg V Maltsev1, Udaya Kiran Marelli1, Tobias G Kapp1, Francesco Saverio Di Leva2, Salvatore Di Maro3, Markus Nieberler4, Ute Reuning5, Markus Schwaiger6, Ettore Novellino2, Luciana Marinelli2, Horst Kessler7.
Abstract
The αvβ6 integrin binds the RGD-containing peptide of the foot and mouth disease virus with high selectivity. In this study, the long binding helix of this ligand was downsized to an enzymatically stable cyclic peptide endowed with sub-nanomolar binding affinity toward the αvβ6 receptor and remarkable selectivity against other integrins. Computational studies were performed to disclose the molecular bases underlying the high binding affinity and receptor subtype selectivity of this peptide. Finally, the utility of the ligand for use in biomedical studies was also demonstrated here.Entities:
Keywords: cyclic peptides; integrin inhibitors; molecular imaging; subtype selectivity; αvβ6 integrin
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Year: 2015 PMID: 26663660 DOI: 10.1002/anie.201508709
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336