Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5506862 | Biochemical and Biophysical Research Communications | 2016 | 6 Pages |
â¢Artificial peptide agonist to FGFR1c/KLB complex is generated.â¢The peptide has no sequence similarity with FGF21.â¢The peptide selectively recognizes the complex interface of FGFR1c/βKlotho and activates the it both in vitro and in vivo.
Fibroblast growth factor receptor-1c (FGFR1c)/βKlotho (KLB) complex is a receptor of fibroblast growth factor 21 (FGF21). Pharmacologically, FGF21 shows anti-obesity and anti-diabetic effects upon peripheral administration. Here, we report the development of an artificial peptide agonist to the FGFR1c/KLB heterodimer complex. The peptide, F91-8A07 (LPGRTCREYPDLWWVRCY), was discovered from random peptide T7 phage display and selectively bound to the FGFR1c/KLB complex, but not to FGFR1c and KLB individually. After subsequent peptide dimerization using a short polyethyleneglycol (PEG) linker, the dimeric F91-8A07 peptide showed higher potent agonist activity than that of FGF21 in cultured primary human adipocytes. Moreover, the dimeric peptide led to an expression of the early growth response protein-1 (Egr-1) mRNA in vivo, which is a target gene of FGFR1c. To the best of our knowledge, this is the first report of a FGFR1c/KLB complex-selective artificial peptide agonist.
Graphical abstractDownload full-size image