Kinetic-Based High-Throughput Screening Assay to Discover Novel Classes of Macrophage Migration Inhibitory Factor Inhibitors

被引:9
|
作者
Ouertatani-Sakouhi, Hajer
Liu, Min [2 ,3 ]
El-Turk, Farah
Cuny, Gregory D. [2 ,3 ]
Glicksman, Marcie A. [2 ,3 ]
Lashuel, Hilal A. [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Swiss Fed Inst Technol, Lab Mol Neurobiol & Funct Neuroprote, Brain Mind Inst,SV LMNN, CH-1015 Lausanne, Switzerland
[2] Brigham & Womens Hosp, Harvard NeuroDiscovery Ctr, Lab Drug Discovery Neurodegenerat, Cambridge, MA USA
[3] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
基金
瑞士国家科学基金会;
关键词
MIF; macrophage migration inhibitory factor; HTS; high throughput screening; tautomerase activity; inflammatory diseases; PHENYLPYRUVATE TAUTOMERASE ACTIVITY; ACTIVE-SITE; FACTOR MIF; DOPACHROME TAUTOMERASE; RHEUMATOID-ARTHRITIS; ANGSTROM RESOLUTION; BIOLOGICAL FUNCTION; ENZYMATIC-ACTIVITY; POTENT INHIBITORS; CRYSTAL-STRUCTURE;
D O I
10.1177/1087057110363825
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Macrophage migration inhibitory factor (MIF) is a major mediator of innate immunity and inflammation and presents a potential therapeutic target for various inflammatory, infectious, and autoimmune diseases, including cancer. Although a number of inhibitors have been identified and designed based on the modification of known nonphysiological substrates, the lack of a suitable high-throughput assay has hindered the screening of chemical libraries and the discovery of more diverse inhibitors. Herein the authors report the development and optimization of a robust high-throughput kinetic-based activity assay for the identification of new MIF inhibitors. Using this assay, they screened 80,000 small molecules and identified and validated 13 novel inhibitors of MIF catalytic activity. These small molecules demonstrated inhibition constant (K-i,K-app) values ranging from 0.5 to 13 mu M. (Journal of Biomolecular Screening 2010: 347-358)
引用
收藏
页码:347 / 358
页数:12
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