A magnetic beads-based ligand fishing method for rapid discovery of monoterpene indoles as monoamine oxidase A inhibitors from Hunteria zeylanica

被引:3
|
作者
Liu, Huaixin [1 ]
Wang, Jincai [1 ]
Yang, Sirui [1 ]
Li, Ziwei [2 ]
Song, Min [2 ]
Zhang, Xiaoqi [2 ]
Crommen, Jacques [3 ]
Jiang, Zhengjin [1 ,2 ]
Zhang, Tingting [1 ]
机构
[1] Jinan Univ, Inst Pharmaceut Anal,Minist Educ MOE China, Coll Pharm,Int Cooperat Lab Tradit Chinese Med Mod, Guangdong Prov Key Lab Pharmacodynam Constituents, Guangzhou 510632, Peoples R China
[2] Jinan Univ, State Key Lab Bioact Mol & Druggabil Assessment, NMPA Key Lab Qual Evaluat TCM, Guangzhou 510632, Peoples R China
[3] Univ Liege, Dept Pharmaceut Sci, Lab Analyt Pharmaceut Chem, CIRM,CHu 836, B-4000 Liege, Belgium
基金
中国国家自然科学基金;
关键词
Magnetic beads; Monoamine oxidase A inhibitors; Ligand fishing; Hunteria zeylanica; Immobilized enzyme; Antidepression; ALKALOIDS; PERFORMANCE; ENZYME; IDENTIFICATION; MOCLOBEMIDE;
D O I
10.1016/j.chroma.2024.464896
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, a novel magnetic bead -based ligand fishing method was developed for rapid discovery of monoterpene indoles as monoamine oxidase A inhibitors from natural products. In order to improve the screening efficiency, two different magnetic beads, i.e. amine and carboxyl terminated magnetic beads, were comprehensively compared in terms of their ability to immobilize monoamine oxidase A (MAOA), biocatalytic activity and specific adsorption rates for affinity ligands. Carboxyl terminated magnetic beads performed better for MAOA immobilization and demonstrated superior performance in ligand fishing. The MAOA immobilized magnetic beads were applied to screen novel monoamine oxidase inhibitors in an alkaloid -rich plant, Hunteria zeylanica . Twelve MAOA affinity ligands were screened out, and ten of them were identified as monoterpene indole alkaloids by HPLC-Obitrap-MS/MS. Among them, six ligands, namely geissoschizol, vobasinol, yohimbol, dihydrocorynanthenol, eburnamine and ( +)-isoeburnamine which exhibited inhibitory activity against MAOA with low IC 50 values. To further explore their inhibitory mechanism, enzyme kinetic analysis and molecular docking studies were conducted.
引用
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页数:9
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