氧化应激
抗氧化剂
合理设计
氧化损伤
氧化磷酸化
对接(动物)
激进的
肽
体外
氧化还原
生物物理学
体内
生物化学
化学
氨基酸
肽序列
组合化学
材料科学
蛋白质结构
分子动力学
结构-活动关系
活性氧
量子化学
KEAP1型
蛋白质-蛋白质相互作用
分子模型
纳米技术
结构母题
生物活性
谷胱甘肽
分子间力
氨基酸残基
密度泛函理论
作者
Jun Ma,Liang Dong,Yanan Li,Kai Xiang,Jiaxin Zou,Hailin Cong,Bing Yu
标识
DOI:10.1021/acsami.5c16317
摘要
Antioxidant peptides (APs) effectively neutralize free radicals and attenuate oxidative stress-related pathologies. However, the structural and conformational determinants underlying their bioactivity remain underexplored. In this study, six APs (AP1–AP6) with the sequence CKC-X-WM were designed, where X represents amino acid residues with distinct physicochemical properties. Quantum chemical calculations and molecular docking elucidated how residue-specific modulation influences redox activity and intermolecular interactions. AP2 and AP4 exhibited superior in vitro and cellular antioxidant capacities, attributed to their optimized orbital energy gaps (4.894 51 and 4.902 13 eV, respectively). In vivo applications demonstrated their efficacy in alleviating oxidative damage in models of diabetes, aging, UV-induced photodamage, and acute alcoholic hepatotoxicity. Computational methods provided mechanistic insights into conformational dynamics, highlighting the multifunctionality of APs. This study advances the rational design of therapeutic peptides and their potential as functional biomaterials for oxidative stress management.
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