Rapid Screening and Identification of BSA Bound Ligands from Radix astragali Using BSA Immobilized Magnetic Nanoparticles Coupled with HPLC-MS

被引:19
|
作者
Liu, Liangliang [1 ]
Leng, Juan [1 ]
Yang, Xiai [1 ]
Liao, Liping [1 ]
Cen, Yin [3 ]
Xiao, Aiping [1 ]
Ma, Lei [2 ]
机构
[1] Chinese Acad Agr Sci, Inst Bast Fiber Crops, Changsha 410205, Hunan, Peoples R China
[2] CAAS, Inst Cotton Res, State Key Lab Cotton Biol, Anyang 455000, Peoples R China
[3] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Hunan, Peoples R China
来源
MOLECULES | 2016年 / 21卷 / 11期
关键词
bovine serum albumin; HPLC-MS; ligands; magnetic nanoparticles; Radix astragali; BOVINE SERUM-ALBUMIN; LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; NATURAL-PRODUCTS; RAT PLASMA; INHIBITORS; EXTRACTION; PROTEIN; ENZYME; HERBS;
D O I
10.3390/molecules21111471
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Radix astragali is widely used either as a single herb or as a collection of herbs in a complex prescription in China. In this study, bovine serum albumin functionalized magnetic nanoparticles (BSA-MN) coupled with high performance liquid chromatography-mass spectrometry (HPLC-MS) were used to screen and identify bound ligands from the n-butanol part of a Radix astragali extract. The prepared BSA-MN showed sufficient magnetic response for the separation with an ordinary magnet and satisfied reusability. Fundamental parameters affecting the preparation of BSA-MN and the screening efficiency were studied and optimized. Under the optimum conditions, four bound ligands were screened out from the n-butanol part of a Radix astragali extract and identified as genistin (1), calycosin-7-O-beta-D-glucoside (2), ononin (3) and formononetin (4). This effective method could be widely applied for rapid screening and identification of active compounds from complex mixtures without the need for preparative isolation.
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页数:13
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