状超分子结网用于对抗神经炎症的酶选择性催化
Congcong Huang1,2, Junlin Ya1,2, Chuanqi Zhao1,2
1Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, P.R. China.
嵌合体结有机框架 (HOFs) 模仿酶,催化不对称合成并显示出优异的抗神经炎症作用. 左手HOF产品通过增强微质细胞功能来缓解阿尔茨海默病的症状.
科学领域:
- 材料化学 材料化学
- 生物模拟催化剂的使用
- 神经科学是一个神经科学.
背景情况:
- 非共价相互作用对于蛋白质功能和酶反应至关重要.
- 网状材料为设计人工酶提供了一个平台.
- 模仿自然的酶微环境是先进催化剂的关键.
研究的目的:
- 构建具有酶模拟能力的性结有机框架 (HOF).
- 研究这些HOFs的阿尔多酶类活性和酶选择性催化.
- 在神经炎症和阿尔茨海默病模型中评估合成的性化合物的体内治疗潜力.
主要方法:
- 合成和结晶结构的确定吉拉HOFs (LHOF和DHOF).
- 不对称的阿尔多尔反应被HOFs催化,产生3-基-1,5-二-1-坦反体.
- 在实验室中评估反应性氧物种 (ROS) 清除活动.
- 使用LPS诱导的炎症和3×Tg-AD小鼠模型进行体内研究,以评估抗神经炎症作用和阿尔茨海默病症状缓解.
主要成果:
- 新型合性HOFs已成功合成并进行结构特征.
- HOFs表现出类似阿尔多酶的活性,催化了生物活性分子的不对称合成.
- 左撇子反体表现出优越的ROS清除和显著的抗神经炎症作用.
- 用奇拉产品治疗逆转了微质细胞表型,增强了Aβ细胞分裂,并减轻了小鼠阿尔茨海默病的症状.
结论:
- 将非共价相互作用引入网状材料中,可以产生有效的人工酶.
- 状HOFs提供了一个有前途的平台,用于enantioselective生物模拟催化.
- 合成的性化合物对阿尔茨海默氏症等神经炎症性疾病具有治疗潜力.
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