AUTHOR=Chan Linda , Smith Craig , Chua Berenice , Lin Feng , Bathgate Ross , Separovic Frances , Gundlach Andrew , Hossain M. Akhter , Wade John TITLE=Synthesis of fluorescent analogs of relaxin family peptides and their preliminary in vitro and in vivo characterization JOURNAL=Frontiers in Chemistry VOLUME=1 YEAR=2013 URL=https://www.frontiersin.org/journals/chemistry/articles/10.3389/fchem.2013.00030 DOI=10.3389/fchem.2013.00030 ISSN=2296-2646 ABSTRACT=
Relaxin, a heterodimeric polypeptide hormone, is a key regulator of collagen metabolism and multiple vascular control pathways in humans and rodents. Its actions are mediated via its cognate G-protein-coupled receptor, RXFP1 although it also “pharmacologically” activates RXFP2, the receptor for the related, insulin-like peptide 3 (INSL3), which has specific actions on reproduction and bone metabolism. Therefore, experimental tools to facilitate insights into the distinct biological actions of relaxin and INSL3 are required, particularly for studies of tissues containing both RXFP1 and RXFP2. Here, we chemically functionalized human (H2) relaxin, the RXFP1-selective relaxin analog H2:A(4-24)(F23A), and INSL3 to accommodate a fluorophore without marked reduction in binding or activation propensity. Chemical synthesis of the two chains for each peptide was followed by sequential regioselective formation of their three disulfide bonds. Click chemistry conjugation of Cy5.5 at the B-chain N-terminus, with conservation of the disulfide bonds, yielded analogs displaying appropriate selective binding affinity and ability to activate RXFP1 and/or RXFP2