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Screening of monoamine oxidase B inhibitors in Tibetan strawberry by ligand fishing based on enzyme functionalized cellulose filter paper
被引:2
作者:

Hu, Yi-Kao
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Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China

Ma, Chao
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Tibet Plateau Inst Biol, Phytochem Lab, Lhasa 850001, Peoples R China Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China

Li, Ming-Jie
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Shenzhen Hujia Technol Co Ltd, HBN Res Inst & Biol Lab, Shenzhen 518000, Peoples R China Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China

Bai, Xiao-Lin
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Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China

Liu, Yi-Ming
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机构:
Jackson State Univ, Dept Chem & Biochem, Jackson, MS 39217 USA Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China

Liao, Xun
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Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China
机构:
[1] Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China
[2] Tibet Plateau Inst Biol, Phytochem Lab, Lhasa 850001, Peoples R China
[3] Shenzhen Hujia Technol Co Ltd, HBN Res Inst & Biol Lab, Shenzhen 518000, Peoples R China
[4] Jackson State Univ, Dept Chem & Biochem, Jackson, MS 39217 USA
基金:
美国国家卫生研究院;
中国国家自然科学基金;
关键词:
Tibetan strawberry;
Cellulose filter paper;
MAO -B inhibitors;
Ligand fishing;
Neuroprotective natural products;
DISEASE;
FRUITS;
D O I:
10.1016/j.microc.2024.110838
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Tibetan strawberry (Fragaria nubicola) is a wild medicinal and edible plant in Tibet possessing various health benefits such as neuroprotection and anti-oxidation. However, there has been little study reported on its chemical constituents. To investigate the inhibitors of monoamine oxidase B (MAO-B) in Tibetan strawberry, we immobilized the enzyme onto cellulose filter paper for the first time to develop a new screening method. Two known glycosides (compounds 1 and 2) and one new iridoid glucoside (Compound 3) were fished out by this method, which was found to effectively inhibit MAO-B with IC50 values of 16.95 +/- 0.93, 24.69 +/- 0.20, and 46.77 +/- 0.78 mu M, respectively. Molecular docking and kinetic analysis were performed to reveal the inhibition mechanism of these compounds. Furthermore, compound 1 exhibited neuroprotective effects against 6-OHDAinduced injury on PC12 cells. The developed method exhibits the advantages of rapidness and effectiveness in screening of MAO-B inhibitors from complex herbal extracts.
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