| Literature DB >> 26954624 |
Kentaro Takayama1, Akari Nakamura1, Cédric Rentier1, Yusaku Mino1, Tomo Asari1, Yusuke Saga1, Akihiro Taguchi1, Fumika Yakushiji1, Yoshio Hayashi2.
Abstract
Inhibition of myostatin, which negatively regulates skeletal muscle growth, is a promising strategy for the treatment of muscle atrophic disorders, such as muscular dystrophy, cachexia and sarcopenia. Recently, we identified peptide A (H-WRQNTRYSRIEAIKIQILSKLRL-NH2 ), the 23-amino-acid minimum myostatin inhibitory peptide derived from mouse myostatin prodomain, and highlighted the importance of its N-terminal tryptophan residue for the effective inhibition. In this study, we synthesized a series of acylated peptide derivatives focused on the tryptophan residue to develop potent myostatin inhibitors. As a result of the investigation, a more potent derivative of peptide A was successfully identified in which the N-terminal tryptophan residue is replaced with a 2-naphthyloxyacetyl moiety to give an inhibitory peptide three times (1.19±0.11 μm) more potent than parent peptide A (3.53±0.25 μm). This peptide could prove useful as a new starting point for the development of improved inhibitory peptides.Entities:
Keywords: TGF-β superfamily; acylation; inhibitors; muscle atrophic disorders; myostatin
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Year: 2016 PMID: 26954624 DOI: 10.1002/cmdc.201500533
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466