Engineering and Characterization of a Long-Half-Life Relaxin Receptor RXFP1 Agonist

Relaxin-2 is a peptide hormone with important roles in human cardiovascular and reproductive biology. Its ability to activate cellular responses such as vasodilation, angiogenesis, and anti-inflammatory and antifibrotic effects has led to significant interest in using relaxin-2 as a therapeutic for heart failure and several fibrotic conditions. However, recombinant relaxin-2 has a very short serum half-life, limiting its clinical applications. Here, we present protein engineering efforts targeting the relaxin-2 hormone in order to increase its serum half-life while maintaining its ability to activate the G protein-coupled receptor RXFP1. To achieve this, we optimized a fusion between relaxin-2 and an antibody Fc fragment, generating a version of the hormone with a circulating half-life of around 3 to 5 days in mice while retaining potent agonist activity at the RXFP1 receptor both in vitro and in vivo.

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Publication Details

Journal
Molecular Pharmaceutics
Published
2024-08-12
DOI
https://doi.org/10.1021/acs.molpharmaceut.4c00368
Citations
7
Primary Topic
Pregnancy-related medical research
Type
article
Field-Weighted Citation Impact
3.26

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article

Engineering and Characterization of a Long-Half-Life Relaxin Receptor RXFP1 Agonist

James Osei‐Owusu, Sarah C. Erlandson, Howard A. Rockman, Andrew C. Kruse et al.
7 citations
Molecular Pharmaceutics
Pregnancy-related medical research
3.26
article

Engineering and Characterization of a Long-Half-Life Relaxin Receptor RXFP1 Agonist

James Osei‐Owusu, Sarah C. Erlandson, Howard A. Rockman, Andrew C. Kruse, Haoran Jiang, Jialu Wang
article en
7 citations

Abstract

Relaxin-2 is a peptide hormone with important roles in human cardiovascular and reproductive biology. Its ability to activate cellular responses such as vasodilation, angiogenesis, and anti-inflammatory and antifibrotic effects has led to significant interest in using relaxin-2 as a therapeutic for heart failure and several fibrotic conditions. However, recombinant relaxin-2 has a very short serum half-life, limiting its clinical applications. Here, we present protein engineering efforts targeting the relaxin-2 hormone in order to increase its serum half-life while maintaining its ability to activate the G protein-coupled receptor RXFP1. To achieve this, we optimized a fusion between relaxin-2 and an antibody Fc fragment, generating a version of the hormone with a circulating half-life of around 3 to 5 days in mice while retaining potent agonist activity at the RXFP1 receptor both in vitro and in vivo.

Molecular PharmaceuticsVol. 21(9)
Harvard University (US), Duke University (US), Boston VA Research Institute (US), Duke Medical Center (US), Duke University Hospital (US)
Damon Runyon Cancer Research Foundation, Harvard Medical School, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences
Openalex Percentile: Top 8%
Pregnancy-related medical research
3.26
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