肌生成抑制素
化学
肽
杜氏肌营养不良
负调节器
内分泌学
内科学
骨骼肌
内生
调节器
氨基酸
肌肉团
生物化学
生物
信号转导
基因
医学
作者
Kentaro Takayama,Yuri Noguchi,Shin Aoki,Shota Takayama,Momoko Yoshida,Tomo Asari,Fumika Yakushiji,Shin‐ichiro Nishimatsu,Yutaka Ohsawa,Fumiko Itoh,Yoichi Negishi,Yoshihide Sunada,Yoshio Hayashi
摘要
Myostatin, an endogenous negative regulator of skeletal muscle mass, is a therapeutic target for muscle atrophic disorders. Here, we identified minimum peptides 2 and 7 to effectively inhibit myostatin activity, which consist of 24 and 23 amino acids, respectively, derived from mouse myostatin prodomain. These peptides, which had the propensity to form α-helix structure, interacted to myostatin with KD values of 30-36 nM. Moreover, peptide 2 significantly increased muscle mass in Duchenne muscular dystrophy model mice.
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