Journal of Medicinal Chemistry · 2017 · 101 citations · 41 references
PharmacyBiochemistryMedicinal ChemistryDrug DesignDrug DiscoveryStructural BiologyG Protein-coupled Receptor SignalingGlucagon-like Peptide-1 Receptor AgonistsLigand BindingPancreatic HormonesPeptide ChemistryPeptide Drug DiscoveryAmino AcidsBlood Glucose RegulationGlucagon Receptor AgonismGlucagon Receptor AgonistsGlucagon-like Peptide 1 Receptor AgonismGlucagon-like PeptidesRational DesignTherapeutic Peptides
Dual activation of the glucagon-like peptide 1 (GLP-1) and glucagon receptor has the potential to lead to a novel therapy principle for the treatment of diabesity. Here, we report a series of novel peptides with dual activity on these receptors that were discovered by rational design. On the basis of sequence analysis and structure-based design, structural elements of glucagon were engineered into the selective GLP-1 receptor agonist exendin-4, resulting in hybrid peptides with potent dual GLP-1/glucagon receptor activity. Detailed structure-activity relationship data are shown. Further modifications with unnatural and modified amino acids resulted in novel metabolically stable peptides that demonstrated a significant dose-dependent decrease in blood glucose in chronic studies in diabetic db/db mice and reduced body weight in diet-induced obese (DIO) mice. Structural analysis by NMR spectroscopy confirmed that the peptides maintain an exendin-4-like structure with its characteristic tryptophan-cage fold motif that is responsible for favorable chemical and physical stability.
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A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management
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