Current advances in screening for bioactive components from medicinal plants by affinity ultrafiltration mass spectrometry

被引:58
作者
Chen, Guilin [1 ,2 ]
Huang, Bill X. [3 ]
Guo, Mingquan [1 ,2 ]
机构
[1] Chinese Acad Sci, Wuhan Bot Garden, Key Lab Plant Germplasm Enhancement & Specialty A, Wuhan 430074, Hubei, Peoples R China
[2] Chinese Acad Sci, Sino Africa Joint Res Ctr, Wuhan 430074, Hubei, Peoples R China
[3] NIAAA, Lab Mol Signaling, NIH, Bethesda, MD USA
关键词
active components; affinity UF-LC; MS; biological targets; high-throughput; medicinal plants; ALPHA-GLUCOSIDASE INHIBITORS; PERFORMANCE LIQUID-CHROMATOGRAPHY; XANTHINE-OXIDASE INHIBITORS; LC-MS; CENTRIFUGAL ULTRAFILTRATION; NEURAMINIDASE INHIBITORS; TOPOISOMERASE-I; SAPOSHNIKOVIA DIVARICATA; DEHYDROGENASE INHIBITORS; LIGAND COMPLEXES;
D O I
10.1002/pca.2769
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
IntroductionMedicinal plants have played an important role in maintaining human health for thousands of years. However, the interactions between the active components in medicinal plants and some certain biological targets during a disease are still unclear in most cases. ObjectiveTo conduct the high-throughput screening for small active molecules that can interact with biological targets, which is of great theoretical significance and practical value. MethodologyThe ultrafiltration mass spectrometry (UF-LC/MS) is a powerful bio-analytical method by combining affinity ultrafiltration and liquid chromatography-mass spectrometry (LC/MS), which could rapidly screen and identify small active molecules that bind to biological targets of interest at the same time. Compared with other analytical methods, affinity UF-LC/MS has the characteristics of fast, sensitive and high throughput, and is especially suitable for the complicated extracts of medicinal plants. ResultsIn this review, the basic principle, characteristics and some most recent challenges in UF-LC/MS have been demonstrated. Meanwhile, the progress and applications of affinity UF-LC/MS in the discovery of the active components from natural medicinal plants and the interactions between small molecules and biological target proteins are also briefly summarised. In addition, the future directions for UF-LC/MS are also prospected. ConclusionAffinity UF-LC/MS is a powerful tool in studies on the interactions between small active molecules and biological protein targets, especially in the high-throughput screening of active components from the natural medicinal plants. The most recent development of UF-MS, and its applications in the identification of targeted bioactive components from medicinal plants have been reviewed. As a highly selective method for bio-affinity capture and high through-put screening, UF-MS is very useful not only for screening of bioactive molecules, but also for the evaluation of the quality, and efficacy of medicinal plants.
引用
收藏
页码:375 / 386
页数:12
相关论文
共 99 条
[1]   Structure-based drug design [J].
Amzel, LM .
CURRENT OPINION IN BIOTECHNOLOGY, 1998, 9 (04) :366-369
[2]   Discovery and resupply of pharmacologically active plant-derived natural products: A review [J].
Atanasov, Atanas G. ;
Waltenberger, Birgit ;
Pferschy-Wenzig, Eva-Maria ;
Linder, Thomas ;
Wawrosch, Christoph ;
Uhrin, Pavel ;
Temml, Veronika ;
Wang, Limei ;
Schwaiger, Stefan ;
Heiss, Elke H. ;
Rollinger, Judith M. ;
Schuster, Daniela ;
Breuss, Johannes M. ;
Bochkov, Valery ;
Mihovilovic, Marko D. ;
Kopp, Brigitte ;
Bauer, Rudolf ;
Dirsch, Verena M. ;
Stuppner, Hermann .
BIOTECHNOLOGY ADVANCES, 2015, 33 (08) :1582-1614
[3]   Molecular recognition of protein-ligand complexes: Applications to drug design [J].
Babine, RE ;
Bender, SL .
CHEMICAL REVIEWS, 1997, 97 (05) :1359-1472
[4]   Thiazole orange as the fluorescent intercalator in a high resolution FID assay for determining DNA binding affinity and sequence selectivity of small molecules [J].
Boger, DL ;
Tse, WC .
BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (09) :2511-2518
[5]  
Calvo E, 2011, EXPERT REV PROTEOMIC, V8, P165, DOI [10.1586/EPR.11.11, 10.1586/epr.11.11]
[6]   Discovery of cyclooxygenase inhibitors from medicinal plants used to treat inflammation [J].
Cao, Hongmei ;
Yu, Rui ;
Choi, Yongsoo ;
Ma, Zhong-Ze ;
Zhang, Hongjie ;
Xiang, Wei ;
Lee, David Yue-Wei ;
Berman, Brian M. ;
Moudgil, Kamal D. ;
Fong, Harry H. S. ;
van Breemen, Richard B. .
PHARMACOLOGICAL RESEARCH, 2010, 61 (06) :519-524
[7]   Isolation of -Amylase Inhibitors from Kadsura longipedunculata Using a High-Speed Counter-Current Chromatography Target Guided by Centrifugal Ultrafiltration with LC-MS [J].
Cen, Yin ;
Xiao, Aiping ;
Chen, Xiaoqing ;
Liu, Liangliang .
MOLECULES, 2016, 21 (09)
[8]   Pulsed ultrafiltration characterization of binding - I. A new method [J].
Chen, CJ ;
Chen, S ;
Woodbury, CP ;
Venton, DL .
ANALYTICAL BIOCHEMISTRY, 1998, 261 (02) :164-182
[9]   Antiproliferative activities of Amaryllidaceae alkaloids from Lycoris radiata targeting DNA topoisomerase I [J].
Chen, Gui-Lin ;
Tian, Yong-Qiang ;
Wu, Jian-Lin ;
Li, Na ;
Guo, Ming-Quan .
SCIENTIFIC REPORTS, 2016, 6
[10]   Screening for Natural Inhibitors of Topoisomerases I from Rhamnus davurica by Affinity Ultrafiltration and High-Performance Liquid Chromatography-Mass Spectrometry [J].
Chen, Guilin ;
Guo, Mingquan .
FRONTIERS IN PLANT SCIENCE, 2017, 8