De novo design and synthesis of cyclic and linear peptides to mimic the binding cassette of human relaxin

Abstract

A synthetic cyclic regioselectively addressable functionalized template was used to prepare six analogs that presented the side chains of the key receptor-binding residues of each of H2 and H3 relaxins and insulin-like peptide 3. None showed any binding affinity for RXFP1, RXFP2, or RXFP3, indicating that the key residues were either incorrectly oriented or that additional residues are required for receptor binding. © 2009 New York Academy of Sciences.