| Literature DB >> 32348108 |
Gregory H Bird1,2, Accalia Fu3,4, Silvia Escudero1,2, Marina Godes1,2, Kwadwo Opoku-Nsiah1,2, Thomas E Wales5, Michael D Cameron6, John R Engen5, Nika N Danial3,7,8, Loren D Walensky1,2,9.
Abstract
Glucagon-like peptide 1 (GLP-1) is a natural peptide agonist of the GLP-1 receptor (GLP-1R) found on pancreatic β-cells. Engagement of the receptor stimulates insulin release in a glucose-dependent fashion and increases β-cell mass, two ideal features for pharmacologic management of type 2 diabetes. Thus, intensive efforts have focused on developing GLP-1-based peptide agonists of GLP-1R for therapeutic application. A primary challenge has been the naturally short half-life of GLP-1 due to its rapid proteolytic degradation in vivo. Whereas mutagenesis and lipidation strategies have yielded clinical agents, we developed an alternative approach to preserving the structure and function of GLP-1 by all-hydrocarbon i, i + 7 stitching. This particular "stitch" is especially well-suited for reinforcing and protecting the structural fidelity of GLP-1. Lead constructs demonstrate striking proteolytic stability and potent biological activity in vivo. Thus, we report a facile approach to generating alternative GLP-1R agonists for glycemic control.Entities:
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Year: 2020 PMID: 32348108 PMCID: PMC7366314 DOI: 10.1021/acschembio.0c00308
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100