Journal article
Distinct activation modes of the Relaxin Family Peptide Receptor 2 in response to insulin-like peptide 3 and relaxin
S Bruell, A Sethi, N Smith, DJ Scott, MA Hossain, QP Wu, ZY Guo, EJ Petrie, PR Gooley, RAD Bathgate
Scientific Reports | NATURE PORTFOLIO | Published : 2017
Abstract
Relaxin family peptide receptor 2 (RXFP2) is a GPCR known for its role in reproductive function. It is structurally related to the human relaxin receptor RXFP1 and can be activated by human gene-2 (H2) relaxin as well as its cognate ligand insulin-like peptide 3 (INSL3). Both receptors possess an N-terminal low-density lipoprotein type a (LDLa) module that is necessary for activation and is joined to a leucine-rich repeat domain by a linker. This linker has been shown to be important for H2 relaxin binding and activation of RXFP1 and herein we investigate the role of the equivalent region of RXFP2. We demonstrate that the linker's highly-conserved N-terminal region is essential for activatio..
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Grants
Awarded by National Science Foundation
Funding Acknowledgements
The authors thank Tania Ferraro and Sharon Layfield for technical assistance. This research was supported by National Health and Medical Research Council of Australia project grants [1043750] and [1100676] (RADB and PRG), the Victorian Government Operational Infrastructure Support Program and equipment grants from the Australian Research Council [LE120100022]. RADB is supported by an NHMRC Research Fellowship.