Department of Medicinal Chemistry, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo 192-0392, Japan.
Org Biomol Chem. 2021 Jan 6;19(1):199-207. doi: 10.1039/d0ob02042g.
For the inhibition of myostatin, which is an attractive strategy for the treatment of muscle atrophic disorders including muscular dystrophy, myostatin-binding peptides were synthesized with an on/off-switchable photooxygenation catalyst at different positions on the peptide chain. These functionalized peptides oxygenated and inactivated myostatin upon irradiation with near-infrared light. Among the peptides tested, a peptide (5) with the catalyst moiety at the 16 position induced myostatin-selective photooxygenation, and efficiently inhibited myostatin. These peptides exhibited low phototoxicity. Such functionalized peptides would provide a precedented strategy for myostatin-targeting therapy, in which myostatin is irreversibly and catalytically inactivated by photooxygenation.
为了抑制肌肉生长抑制素(myostatin),这是一种治疗包括肌肉萎缩症在内的肌肉萎缩性疾病的有吸引力的策略,研究人员在肽链的不同位置合成了具有开/关可切换光氧化催化剂的肌肉生长抑制素结合肽。这些功能化肽在近红外光照射下发生光氧化反应,使肌肉生长抑制素失活。在测试的肽中,位于 16 位的催化剂部分的肽(5)诱导肌肉生长抑制素选择性光氧化,并有效地抑制肌肉生长抑制素。这些肽表现出低光毒性。这种功能化肽为肌肉生长抑制素靶向治疗提供了一个先例,通过光氧化反应使肌肉生长抑制素不可逆和催化失活。