| Literature DB >> 27595986 |
Ying Wang1, Jintang Du1, Huafei Zou1, Yan Liu1, Yuhan Zhang1, Jose Gonzalez1, Elizabeth Chao1, Lucy Lu1, Pengyu Yang1, Holly Parker1, Van Nguyen-Tran1, Weijun Shen1, Danling Wang1, Peter G Schultz2, Feng Wang3.
Abstract
Glucagon-like peptide-1 (GLP-1) receptor (GLP-1R), glucagon (GCG) receptor (GCGR), and glucose-dependent insulinotropic polypeptide (GIP, also known as gastric inhibitory polypeptide) receptor (GIPR), are three metabolically related peptide hormone receptors. A novel approach to the generation of multifunctional antibody agonists that activate these receptors has been developed. Native or engineered peptide agonists for GLP-1R, GCGR, and GIPR were fused to the N-terminus of the heavy chain or light chain of an antibody, either alone or in pairwise combinations. The fusion proteins have similar in vitro biological activities on the cognate receptors as the corresponding peptides, but circa 100-fold longer plasma half-lives. The GLP-1R mono agonist and GLP-1R/GCGR dual agonist antibodies both exhibit potent effects on glucose control and body weight reduction in mice, with the dual agonist antibody showing enhanced activity in the latter.Entities:
Keywords: antibodies; dual agonists; obesity; peptides; protein engineering
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Year: 2016 PMID: 27595986 DOI: 10.1002/anie.201606321
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336