| Literature DB >> 27717820 |
Kotaro Sakamoto1, Yayoi Kawata2, Yasushi Masuda2, Tadashi Umemoto2, Takashi Ito2, Taiji Asami2, Shiro Takekawa2, Tetsuya Ohtaki2, Hiroshi Inooka2.
Abstract
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.Entities:
Keywords: Agonist; FGF21; FGFR; Peptide; Phage display; βKlotho
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Year: 2016 PMID: 27717820 DOI: 10.1016/j.bbrc.2016.10.009
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575