Organic & Biomolecular Chemistry · 2013 · 11 citations · 29 references
PharmacyBiochemistryMedicinal ChemistryDrug DesignDrug DiscoveryStructural BiologyMacromolecular AssemblyPeptide ChemistryPeptide Drug DiscoveryPeptidomimetic DesignProtein StructureProteolytic ProcessingAmide LinkersBeta-sheet MimicsBiomedical ApplicationsProteolytic StabilityProteolytic Stability ControlSelf-assembling MaterialsStructure-based Peptidomimetics
In this study we present the design and synthesis of a novel class of peptidomimetics, the β(3R3)-peptides. Via alternating directions of the amide bonds along β-peptide sequences, β(3R3)-peptides can potentially extend the structural space available to β-peptidic foldamers. Detailed analysis at the air-water interface shows strand conformations and the formation of sheet assemblies with different degrees of crystallinity. Furthermore β(3R3)-peptides exhibit a high proteolytic stability thus making them an interesting new class of peptidomimetics for biomedical applications.
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Samuel H. Gellman · Accounts of Chemical Research · 1998 · 2.5K citations
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Ivan Huc · European Journal of Organic Chemistry · 2003 · 698 citations
Foldamers with Heterogeneous Backbones
W. Seth Horne, Samuel H. Gellman · Accounts of Chemical Research · 2008 · 682 citations · Full text