Discovery of Novel Inhibitors of the Tautomerase Activity of Macrophage Migration Inhibitory Factor (MIF)

被引:13
作者
Cleofe Zapatero, Maria [1 ]
Perez, Paloma [1 ]
Jesus Vazquez, Maria [1 ]
Colmenarejo, Gonzalo [1 ]
de los Frailes, Maite [1 ]
Ramon, Fernando [1 ]
机构
[1] GSK, Ctr Invest Basica, Mol Discovery Res, Santiago Grisolia 4, Madrid 28760, Spain
关键词
macrophage migration inhibitory factor; MIF; high-throughput screening; tautomerase; 4-hydroxyphenylpyruvic acid; l-dopachrome methyl ester; DOPACHROME TAUTOMERASE; DISEASE; TAUTOMERIZATION; MECHANISMS; ENZYME; TARGET; ACID; SITE;
D O I
10.1177/1087057116633997
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 proinflammatory cytokine associated with multiple diseases, including neurodegenerative disorders. With the ultimate goal of providing novel chemotypes as starting points for development of disease-modifying therapeutics for neurodegeneration, we endeavored to screen the GSK compound collection for MIF inhibitors using a miniaturized, activity-based kinetic assay. The assay monitors the increase in absorbance at 320 nm resulting from keto-to-enol tautomerization of 4-hydroxyphenylpyruvate, a reaction catalyzed by MIF. We ran a full-diversity screen evaluating the inhibitory activity of 1.6 million compounds. Primary hits were confirmed and retested in an orthogonal assay measuring tautomerization of l-dopachrome methyl ester by the decrease in absorbance at 475 nm in kinetic mode. Selected compounds were progressed to medium-throughput mode-of-inhibition studies, which included time dependence, enzyme concentration dependence, and reversibility of their inhibitory effect. With these results and after inspection of the physicochemical properties of compounds, 17 chemotypes were prioritized and progressed to further stages of validation and characterization to better assess their therapeutic potential.
引用
收藏
页码:446 / 458
页数:13
相关论文
共 30 条
[1]   MIF as a disease target: ISO-I as a proof-of-concept therapeutic [J].
Al-Abed, Yousef ;
VanPatten, Sonya .
FUTURE MEDICINAL CHEMISTRY, 2011, 3 (01) :45-63
[2]  
[Anonymous], 1989, ANALYST, V114, P1693, DOI DOI 10.1039/AN9891401693
[3]   REGULATION OF THE FINAL PHASE OF MAMMALIAN MELANOGENESIS - THE ROLE OF DOPACHROME TAUTOMERASE AND THE RATIO BETWEEN 5,6-DIHYDROXYINDOLE-2-CARBOXYLIC ACID AND 5,6-DIHYDROXYINDOLE [J].
AROCA, P ;
SOLANO, F ;
SALINAS, C ;
GARCIABORRON, JC ;
LOZANO, JA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 208 (01) :155-163
[4]   SPECIFICITY OF DOPACHROME TAUTOMERASE AND INHIBITION BY CARBOXYLATED INDOLES - CONSIDERATIONS ON THE ENZYME ACTIVE-SITE [J].
AROCA, P ;
SOLANO, F ;
GARCIABORRON, JC ;
LOZANO, JA .
BIOCHEMICAL JOURNAL, 1991, 277 :393-397
[5]   Biochemical and nutational investigations of the enzymatic activity of macrophage migration inhibitory factor [J].
Bendrat, K ;
AlAbed, Y ;
Callaway, DJE ;
Peng, T ;
Calandra, T ;
Metz, CN ;
Bucala, R .
BIOCHEMISTRY, 1997, 36 (49) :15356-15362
[6]   Electrochemical study on the keto-enol tautomerization of p-hydroxyphenylpyruvic acid in aqueous solution [J].
Chi, YW ;
Duan, JP ;
Qi, XZ ;
Chen, GN .
BIOELECTROCHEMISTRY, 2003, 60 (1-2) :37-45
[7]  
Coma I, 2009, METHODS MOL BIOL, V565, P69, DOI 10.1007/978-1-60327-258-2_4
[8]   Discovery of Human Macrophage Migration Inhibitory Factor (MIF)-CD74 Antagonists via Virtual Screening [J].
Cournia, Zoe ;
Leng, Lin ;
Gandavadi, Sunilkumar ;
Du, Xin ;
Bucala, Richard ;
Jorgensen, William L. .
JOURNAL OF MEDICINAL CHEMISTRY, 2009, 52 (02) :416-424
[9]   Multiplexed Immunoassay Panel Identifies Novel CSF Biomarkers for Alzheimer's Disease Diagnosis and Prognosis [J].
Craig-Schapiro, Rebecca ;
Kuhn, Max ;
Xiong, Chengjie ;
Pickering, Eve H. ;
Liu, Jingxia ;
Misko, Thomas P. ;
Perrin, Richard J. ;
Bales, Kelly R. ;
Soares, Holly ;
Fagan, Anne M. ;
Holtzman, David M. .
PLOS ONE, 2011, 6 (04)
[10]   Inhibition of MIF bioactivity by rational design of pharmacological inhibitors of MIF tautomerase activity [J].
Dios, A ;
Mitchell, RA ;
Aljabari, B ;
Lubetsky, J ;
O'Connor, K ;
Liao, H ;
Senter, PD ;
Manogue, KR ;
Lolis, E ;
Metz, C ;
Bucala, R ;
Callaway, DJE ;
Al-Abed, Y .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (12) :2410-2416