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.
Authors
- James Osei‐Owusu (ORCID: https://orcid.org/0000-0002-8676-4444)
- Sarah C. Erlandson
- Howard A. Rockman (ORCID: https://orcid.org/0000-0003-2921-1584)
- Andrew C. Kruse (ORCID: https://orcid.org/0000-0002-1467-1222)
- Haoran Jiang (ORCID: https://orcid.org/0000-0001-5916-3072)
- Jialu Wang (ORCID: https://orcid.org/0009-0002-4866-4706)
Institutions
- Harvard University (US)
- Duke University (US)
- Boston VA Research Institute (US)
- Duke Medical Center (US)
- Duke University Hospital (US)
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
Funders
- Damon Runyon Cancer Research Foundation
- Harvard Medical School
- National Institutes of Health
- National Heart, Lung, and Blood Institute
- National Institute of General Medical Sciences