氧化折叠
氧化磷酸化
二硫键
折叠(DSP实现)
化学
蛋白质折叠
计算生物学
组合化学
杠杆(统计)
蛋白质工程
纳米技术
合理设计
生物化学
拟肽
氧化损伤
生物物理学
氧化应激
药物发现
肽
生物信息学
蛋白质结构
作者
Xueting Cheng,Chuanliu Wu
出处
期刊:Chemical Science
[Royal Society of Chemistry]
日期:2025-01-01
卷期号:16 (41): 19012-19025
被引量:8
摘要
, ziconotide for chronic pain and insulin for diabetes). However, DRP functionality critically depends on native oxidative folding, where inefficient disulfide pairing causes low production yields, induces functional instability through disulfide isomerizations, and triggers misfolding upon sequence engineering. Recent advances in directed oxidative folding permit precise pathway control, facilitating efficient engineering and discovery of functional DRPs, thereby accelerating diagnostic and therapeutic development. Herein, we summarize novel strategies that actively direct the oxidative folding of DRPs to enhance their engineering and applications. Additionally, we present our perspective on key challenges in DRP design and discovery associated with oxidative folding, and propose future research directions to advance this field.
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