High-performance liquid chromatography assay with fluorescence detection for the evaluation of inhibitors against human recombinant monoacylglycerol lipase

被引:26
作者
Holdrerich, Angela [1 ]
Makharadze, Teona [1 ]
Lehr, Matthias [1 ]
机构
[1] Univ Munster, Inst Pharmaceut & Med Chem, D-48149 Munster, Germany
关键词
Monoacylglycerol lipase; Inhibitors; Pyrene-substituted; 2-acylglycerol; Rearrangement; HPLC; Fluorescence detection; ACID AMIDE HYDROLASE; ULTRAVIOLET SPECTROMETRIC DETECTION; CYTOSOLIC PHOSPHOLIPASE A(2); RAT CEREBELLAR MEMBRANES; MONOGLYCERIDE LIPASE; ENDOCANNABINOID; 2-ARACHIDONOYLGLYCEROL; ENZYME-INHIBITORS; HYDROLYSIS; ANALOGS; GLYCEROL;
D O I
10.1016/j.ab.2009.12.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fluorescent assay for the evaluation of inhibitors of monoacylglycerol lipase (MAGL) is described. 1,3-Dihydroxypropan-2-yl 4-pyren-1-ylbutanoate was designed and synthesized as novel fluorogenic substrate. Activity of human recombinant MAGL was determined in the presence of the surfactant Triton X-100 without further sample cleanup by measuring the amount of 4-pyren-1-ylbutanoic acid released by the enzyme with reversed-phase high-performance liquid chromatography (HPLC) and fluorescence detection. The known covalent binding MAGL inhibitors methyl arachidonyl fluorophosphonate (MAFP), 4-nitrophenyl 4-[bis(1,3-benzodioxol-5-yl)hydroxymethyl]piperidine-1-carboxylate (JZL184), and [4-(5-methoxy-2-oxo-1,3,4-oxadiazol-3-yl)-2-methylphenyl]carbamic acid benzyl ester(CAY10499) were used to validate the test system. Applying an incubation time of 15 min, the IC50 values obtained for these compounds were 0.16, 3.7, and 1.1 mu M, respectively. A prolongation of the incubation to 45 min results in a two- to threefold decrease of the IC50 values. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:218 / 224
页数:7
相关论文
共 39 条
  • [1] Development of a potent inhibitor of 2-arachidonoylglycerol hydrolysis with antinociceptive activity in vivo
    Bisogno, Tiziana
    Ortar, Giorgio
    Petrosino, Stefania
    Morera, Enrico
    Palazzo, Enza
    Nalli, Marianna
    Maione, Sabatino
    Di Marzo, Vincenzo
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2009, 1791 (01): : 53 - 60
  • [2] A comprehensive profile of brain enzymes that hydrolyze the endocannabinoid 2-arachidonoylglycerol
    Blankman, Jacqueline L.
    Simon, Gabriel M.
    Cravatt, Benjamin F.
    [J]. CHEMISTRY & BIOLOGY, 2007, 14 (12): : 1347 - 1356
  • [3] Kinetics of acyl migration in monoglycerides and dependence on acyl chainlength
    Boswinkel, G
    Derksen, JTP
    vantRiet, K
    Cuperus, FP
    [J]. JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1996, 73 (06) : 707 - 711
  • [4] A novel assay for mono acylglycerol hydrolysis suitable for high-throughput screening
    Brengdahl, Johan
    Fowler, Christopher J.
    [J]. ANALYTICAL BIOCHEMISTRY, 2006, 359 (01) : 40 - 44
  • [5] Brain monoglyceride lipase participating in endocannabinoid inactivation (vol 99, pg 10819, 2002)
    Dinh, TP
    Carpenter, D
    Leslie, FM
    Freund, TF
    Katona, I
    Sensi, SL
    Kathuria, S
    Piomelli, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (21) : 13961 - 13961
  • [6] Even L., 2008, [No title captured], Patent No. [2008145839, WO 2008/145839, PCT/FR2008/000532]
  • [7] Determination of prostaglandin E2 by on-line solid-phase extraction-liquid chromatography with ultraviolet detection for microsomal prostaglandin E2 synthase-1 inhibitor screening
    Fabian, Joerg
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2008, 875 (02): : 557 - 561
  • [8] High-performance liquid chromatographic assay with fluorescence detection for the evaluation of inhibitors against fatty acid amide hydrolase
    Forster, Laura
    Elfringhoff, Alwine Schulze
    Lehr, Matthias
    [J]. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2009, 394 (06) : 1679 - 1685
  • [9] Inhibition of monoacylglycerol lipase and fatty acid amide hydrolase by analogues of 2-arachidonoylglycerol
    Ghafouri, N
    Tiger, G
    Razdan, RK
    Mahadevan, A
    Pertwee, RG
    Martin, BR
    Fowler, CJ
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2004, 143 (06) : 774 - 784
  • [10] Trifluoromethyl ketones and methyl fluorophosphonates as inhibitors of group IV and VI phospholipases A2:: structure-function studies with vesicle, micelle, and membrane assays
    Ghomashchi, F
    Loo, R
    Balsinde, J
    Bartoli, F
    Apitz-Castro, R
    Clark, JD
    Dennis, EA
    Gelb, MH
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1999, 1420 (1-2): : 45 - 56