Conference Proceedings
Resolving the unconventional mechanisms underlying RXFP1 and RXFP2 receptor function
BJ Hartley, DJ Scott, GE Callander, TN Wilkinson, DE Ganella, CK Kong, S Layfield, T Ferraro, EJ Petrie, RAD Bathgate
Annals of the New York Academy of Sciences | WILEY-BLACKWELL | Published : 2009
Abstract
The receptors for relaxin and insulin-like peptide 3 (INSL3) are now well-characterized as the relaxin family peptide (RXFP) receptors RXFP1 and RXFP2, respectively. They are G-protein-coupled receptors (GPCRs) with closest similarity to the glycoprotein hormone receptors, with both containing large ectodomains with 10 leucine-rich repeats (LRRs). Additionally, RXFP1 and RXFP2 are unique in the LGR family in that they contain a low-density lipoprotein class A (LDL-A) module at their N-terminus. Ligand-mediated activation of RXFP1 and RXFP2 is a complex process involving various domains of the receptors. Primary ligand binding occurs via interactions between B-chain residues of the peptides w..
View full abstractRelated Projects (3)
Grants
Awarded by National Health and Medical Research Council of Australia
Funding Acknowledgements
Ross Bathgate is the recipient of a Senior Research Fellowship from the National Health and Medical Research Council of Australia (NHMRC 509011). This work was Supported by project grants 300012 and 454375 from the NHMRC.