Novel LC/MS/MS and High-Throughput Mass Spectrometric Assays for Monoacylglycerol Acyltransferase Inhibitors

Materials and Reagents

1-Decanoyl-rac-glycerol, decanoyl coenzyme A, and fatty acid–free bovine serum albumin (FAF-BSA) were purchased from Sigma-Aldrich (St. Louis, MO). Verapamil was purchased from Enzo Life Sciences (Farmingdale, NY). 1,2-Didecanoyl-glycerol and 1,3-didecanoyl-glycerol were purchased from Nu-Chek Prep (Waterville, MN). Pooled CD-1 mouse, Sprague Dawley rat, beagle dog, cynomolgus monkey, and human intestinal microsomes were obtained from XenoTech (Kansas City, KS).

Enzyme and Substrate Mixture Preparation

Recombinant human MGAT2 was produced in the baculovirus expression system. Sf9 insect cells were infected for 72 h. Cell pellets were resuspended in homogenization buffer (0.1 M sucrose, 50 mM KCl, 40 mM KH₂PO₄, 30 mM EDTA, pH 7.2). After centrifugation at 2500×g for 15 min at 4 °C, the pellet was resuspended in 500 ml lysis buffer, and total cell membranes were collected by ultracentrifugation at 100,000×g for 60 min at 4 °C. The collected membranes were resuspended in homogenization buffer and stored in aliquots at −80 °C. 1-Decanoyl-rac-glycerol was dissolved in 100% acetone at a stock concentration of 20 mM and stored in aliquots at −20 °C. Decanoyl-coenzyme A was dissolved in 0.1 M sodium acetate, pH 4.0, at 10 mM and stored in aliquots at −20 °C.

Recombinant MGAT2 Assay

In this assay, the MGAT2 enzyme catalyzed the production of didecanoyl-glycerol starting from 1-decanoyl-rac-glycerol and decanoyl-CoA. Didecanoyl-glycerol was detected by LC/MS/MS in a 384-well format. Briefly, 100 nl of compounds was dispensed to a 384-well polypropylene plate by the [Q1]Hummingbird. MGAT2 activity in membrane preparations was assayed in 50 mM KH₂PO4 (pH 7.4), 0.02% BSA, 1 mM DTT, 40 ng/ml MGAT2 membranes, 50 µM decanoyl-CoA, 70 µM 1-decanoyl-rac-glycerol, 0.5% acetone, and 0.5% DMSO, in a total reaction volume of 20 µl. The reaction was stopped by adding 60 µl acetonitrile containing 0.8 nM verapamil as an internal standard. After a brief mixing, the plate was centrifuged at 800×g for 5 min. The reaction product 1,3-didecanoyl-glycerol was quantified by LC/MS/MS or HTMS as described below.

Intestinal Microsome MGAT LC/MS/MS Assay

MGAT activity in intestinal microsomes of mice, rats, dogs, monkeys, and humans was assayed in 50 mM KH₂PO4 (pH 7.4), 0.02% BSA, 1 mM DTT, indicated concentrations of human MGAT (hMGAT) or intestinal microsomes, 50 µM decanoyl-CoA, 70 µM 1-decanoyl-rac-glycerol, and 0.5% acetone, in a total reaction volume of 20 µl. The reaction was stopped by adding 60 µl acetonitrile containing 0.8 nM verapamil as an internal standard. After a brief mixing, the plate was centrifuged at 800×g for 5 min. The reaction product 1,3-didecanoyl-glycerol was quantified by LC/MS/MS as described below.

Product Detection by LC/MS/MS

The reaction product 1,3-didecanoyl-glycerol is quantified by LC/MS/MS using an Agilent 1100 HPLC system interfaced with a Waters Micromass Quattro Ultima triple quadrupole mass spectrometer (Waters, Milford, MA) equipped with an electrospray ionization source. The experimental conditions included the following parameters. A Zorbax SB-C8 column (2.1 × 50 mm and 3.5 µm particle size) was used. The column temperature was 60 °C. Buffer A consisted of 4 mM ammonium formate and 0.1% formic acid in water. Buffer B consisted of acetonitrile–water (90:10) containing 4 mM ammonium formate and 0.1% formic acid. The flow rate was 0.6 ml/min. A gradient elution had an initial ratio of 60:40 (A:B), then ramped to 100% B in 0.5 min, held for 1.5 min, and returned to initial conditions for a total run time of 3 min. A positive-ion mode was used for this multiple reaction monitoring (MRM). The mass analyzer was set for a selected reaction monitoring (SRM) transition for analyte of m/z 383 to 155 with a dwell time of 0.1 sec per transition. The internal standard used was verapamil (0.8 nM), with an SRM transition of m/z 455 to 165. The sample size used was 5 µL. The collision voltage was +25 V, and the capillary voltage was +3.1 kV. AUC (area under the curve) for the product was reported using MassLynx 4.0 software. Calibration curves were generated using synthetic 1,3-didecanoyl-glycerol or 1,2-didecanoyl-glycerol as standards (range: 0.004 µM to 48 µM).

For separation of the 1,2-didecanoyl glycerol from 1,3-didecanoyl glycerol ( Figure 1B ), the following LC conditions were used. Buffer solutions A and B, column temperature, flow rate, and mass spectral parameters are as described above. The column used was a Zorbax 300SB-C8, 2.1 × 150 mm with 3.5 µm particle size. The gradient elution used had an initial ratio of 30% B, then ramped to 75% B in 27 min, then returned stepwise to 30% B for 30 min.

OPEN IN VIEWER

Figure 1.

(A) Chemical structure of the protonated dehydro-1,3 didecanoyl glycerol, which was the MS-induced precursor for selected reaction monitoring (SRM) detection of enzyme product as shown. The transition m/z 383 to m/z 155 was used for mass spectrometry (MS)-based quantitation. (B) SRM ion chromatograms: (a) 1,3-didecanoyl glycerol standard; (b) 1,2-didecanoyl glycerol standard; (c) a 1:1 mixture of 1,3- and 1,2-didecanoyl glycerol standards; and (d) the monoacylglycerol acyltransferase enzyme product MGAT2. Note that all transitions were from the dehydrated form of the diacylglycerol that was MS induced.

Product Detection by HTMS

The reaction product 1,3-didecanoyl-glycerol was quantified using a RapidFire 300 inlet system (Agilent) coupled to a Sciex 4000 triple quadrupole mass spectrometer (Sciex, Toronto, Canada). The mobile phase was 15 mM ammonium formate and 0.1% formic acid in acetonitrile–water (1:1). The wash solvent used was isopropanol–water (1:1). The wash between samples was 500 ms. The sample aspiration time (state 1) was 200 ms (600 ms with sip sensor), and the sample wash time (state 2) was 3000 ms. The sample elution time (state 3) was 3000 ms. The column equilibration time (state 4) was 500 ms. The flow rates used were pump 1 = 1.5 mL/min, and pump 2 and 3 = 1.25 mL/min. The Sciex 4000 mass spectrometer parameters included an SRM transition for didecanoyl glycerol at m/z 418.6 to 229 with 100 ms dwell time, declustering potential = 50 V, entrance potential = 5 V, collision energy = 20 V, and collision cell exit potential = 20 V; for the internal standard (verapamil), the SRM used was m/z 455 to 165 with a dwell time of 100 ms, a declustering potential of 100 V, entrance potential = 9 V, collision energy = 40 V, and collision cell exit potential = 15 V. Other parameters included: positive-ion mode; curtain gas = 20; collisionally activated dissociation gas = medium; ion spray voltage = 5500 V; source temperature = 550 °C; ion source gas 1 = 50; ion source gas 2 = 50; and resolution for Q1/Q3 = low/low. Note that the SRM transition m/z 418 to 229 was a result of neutral loss of decanoic acid from the ammonium adduct ion of 1,3-didecanoyl glycerol.

Development of LC/MS/MS-Based MGAT2 Assays

Zhang et al. recently reported a LC/MS/MS-based DGAT1 membrane activity assay by combining two DGAT1 substrates, di-oleoyl-glycerol and oleoyl-CoA. The product triolein was detected by multiparallel liquid chromatography coupled with LC/MS/MS in a 384-well format. ⁹ We have previous published DGAT1 and DGAT2 activity assays by measuring DGAT-catalyzed formation of TG using 1,2-dicapryl-sn-glycerol and oleoyl-CoA as substrates. The product carrying two capryl side chains and one oleoyl side chain, TG-(C10:0, C10:0, C18:1), was detected by HTMS in a 384-well format. ¹⁰ To date, no MGAT LC/MS/MS assay was reported in the literature. The MGAT activity has been determined routinely by quantifying radiolabeled DAG.^1>–8 Microsomal membrane preparations typically contained endogenous DGAT from the host cells, and these DGAT activities could further acylate the radiolabeled DAG to form radiolabeled TG. A conventional MGAT2 assay using radiolabeled decanoyl-CoA with 2-oleoyl-glycerol or 1-decanoyl-glycerol is shown in Supplemental Figure S1. We observed that MGAT2-catalyzed formation of DAG (C10:0, C10:0) was not further acylated to TG (C10:0, C10:0, C10:0) when 1-decanoyl-glycerol was present. The LC/MS/MS MGAT assay described here used short-chain fatty-CoA (e.g. octanoyl-CoA, decanoyl-CoA, and lauroyl-CoA) and short-chain monoacylglycerol (e.g. 1-decanoyl-rac-glycerol or 1-octanoyl-rac-glycerol) to form DAG containing two short fatty acyl groups (Supplemental Figure S2). The MGAT2 reaction performed in a 384-well format was quenched by adding three volumes of acetonitrile containing an internal standard verapamil. The short side-chain DAGs were less lipophilic and therefore were soluble in a single phase of 3:1 acetonitrile–water mixture. The reaction products were selectively analyzed by LC/MS/MS using the MRM mode ( Figure 1 ). MRM used a triple quadrupole MS/MS instrument to selectively pass a selected precursor ion (i.e., protonated dehydro-1,3 didecanoyl glycerol, m/z 383) and detected a selected product ion at m/z 155. The use of MRM quantification by combining two selection events allowed greater selectivity as well as high sensitivity. Interestingly, when 1-decanoyl-rac-glycerol and decanoyl-CoA were used as MGAT2 substrates, the majority of DAG product was 1,3-didecanoyl glycerol as compared to the 1,3-didecanoyl glycerol or 1,2-didecanoyl glycerol standard ( Figure 1 ). DGAT was known to mediate acylation of DAG at the 3 position. The observation of no TG product in the MGAT2 TLC assay in which 1-decanoyl-glycerol and ¹⁴C-decanoyl-CoA were used as substrates (Supplemental Figure S1) supports the notion that 1,3-didecanoyl glycerol is resistant to further acylation to TG by endogenous DGAT activity in the microsomal preparation and/or the DGAT activity possessed by MGAT.

We also explored the combination of other short-chain acyl-CoA (e.g., octanoyl-CoA, decanoyl-CoA, and lauroyl-CoA) and short-chain monoacylglycerols (e.g., 1-decanoyl-rac-glycerol and 1-octanoyl-rac-glycerol) as MGAT2 substrates. MGAT2 enzyme products of 1-decanoyl-3-lauroyl glycerol (C10:0-C12:0), 1-decanoyl-3-octanoyl glycerol (C10:0-C8:0), or 1-octanoyl-3-lauroyl glycerol (C8:0-C12:0) were successfully detected by LC/MS/MS (Supplemental Figure S3). It was generally observed that each of these disubstituted glycerols could generate both acyl carbonium ions from their constituent fatty acids as product ions, and their structures were correspondingly similar to that shown in Figure 1A for the decanoyl carbonium ion at m/z 155.

Development and Optimization of an MGAT2 HTMS Assay

Although our MGAT2 LC/MS/MS assay was in a 384-well format, it required 2 min run time for each well. In the HTMS assay, MGAT2-catalyzed formation of didecanoyl-glycerol was quantified by HTMS detection in positive mode using the SRM m/z 418 to 229. The use of HTMS shortened MS detection time to 10 sec for a well. Note that the SRM transition m/z 418–229 was a result of neutral loss of decanoic acid from the ammonium adduct ion of 1,3-didecanoyl glycerol. It was observed that the most abundant transition for 1,3-didecanolyl glycerol was different between the LC/MS/MS and HTMS assays depending on which spectrometer was used. This is likely due to a combination of differences in ion source and collision cell design and operating parameters between the Waters Quattro Ultima and Sciex 4000 mass spectrometers.

Figure 2A shows the Km determination of decanoyl-CoA and 1-decanoyl-glycerol in the MGAT2-catalyzed enzymatic reaction. The substrate Km values for 1-decanoyl-rac-glycerol and decanoyl-CoA in MGAT2 HTMS were 40 µM and 18 µM, respectively. These Km values for 1-decanoyl-rac-glycerol and decanoyl-CoA are close to the observed Km values for 2-monooleoyl-glycerol and oleoyl-CoA in the radiolabeled MGAT2 TLC assay. ¹ The reaction kinetic and enzyme titrations are shown in Figure 2B and Figure 2C . A linear time course was observed at least up to 40 min. From these experiments, the enzyme concentration and the reaction time were set at 40 ng/ml and 30 min, respectively. Figure 3 shows Z prime values and their distribution of the HTS plates. The signal-to-background ratio was 8. This MGAT2 HT/MS has been applied successfully in an MGAT2 HTS campaign with nearly 310,000 compounds with a hit rate of 0.47% at 7 µM screening concentration, and a confirmation rate was 49%. Several chemotypes of MGAT2 inhibitors were discovered. As an example, the inhibition of the enzyme product DAG (C10:0, C10:0) by two MGAT2 inhibitors was demonstrated ( Figure 3 ). The IC₅₀ values of JNJ-MGAT2-A and JNJ-MGAT2-B were determined as 40.7 ± 17.2 nM (n = 3, SEM) amd 223.9 ± 54.0 nM (n = 3, SEM), respectively ( Figure 3 ).

OPEN IN VIEWER

Figure 2.

(A) (a) Km determination of decanoyl-CoA at fixed decanoyl-glycerol (Km = 18 µM). (b) Km determination of decanoyl-glycerol at fixed decanoyl-CoA (Km = 40 µM). (B) (a) Time course of the monoacylglycerol acyltransferase enzyme MGAT2’s reaction at 0, 10, 20, 40, 80, and 160 ng/ml MGAT2. (b) MGAT2 concentration dependence of the MGAT2 high-throughput mass spectrometry (HTMS) assay. (C) (a) Inhibition curve and structure of JNJ-MGAT2-A. A representative experiment with duplicate measurement is shown. (b) Inhibition curve of JNJ-MGAT2-B. Two representative experiments are shown.

OPEN IN VIEWER

Figure 3.

(A) Z’ values of the monoacylglycerol acyltransferase enzyme MGAT2 high-throughput mass spectrometry (HTMS) screen by plates. (B) Distribution of Z’ values of the MGAT2 HTMS screening plates.

Intestinal Microsome MGAT LC/MS/MS Assay

Because MGAT activity is highest in the intestines, we evaluated MGAT activity in the intestinal microsomes from mice, rats, dogs, monkeys, and humans using decanoyl-CoA and 1-decanoyl-glycerol as substrates. The robust MGAT activity was found in the intestinal microsomes of all these species ( Figure 4 ). As an example, the inhibition of DAG (C10:0, C10:0) in the MGAT assay with the mouse, rat, dog, and human intestinal microsomes was shown, and ~90% inhibition of total MGAT activity was achieved at 10 µM, the highest concentration tested ( Figure 4 ). The calculated IC₅₀ values of JNJ-MGAT2-B in the MGAT assay with mouse or rat intestinal microsomes were 109 ± 14 nM (n = 2, SEM) and 121 ± 24 nM (n = 2, SEM), respectively. JNJ-MGAT2-A had an IC₅₀ value of 10 nM in the mouse microsomal MGAT assay. The robustness of the MGAT activity using native intestinal microsomes indicates that our MGAT LC/MS/MS assay can be applied to other native tissue preparations.

OPEN IN VIEWER

Figure 4.

(A) Assay for the monoacylglycerol acyltransferase enzyme MGAT’s activity of pooled intestinal microsomes from mice, rats, dogs, monkeys, and humans. The MGAT assay was performed as described in the Method section. (B) Evaluation of an MGAT2 inhibitor in the MGAT assay using mouse, rat, dog, or human intestinal microsomes. A representative experiment is shown.

Recent studies suggest that the significant increase of MGAT1 (MOGAT1) expression in liver and hepatic MGAT activity was responsible for the early onset of type 2 diabetes associated with hepatic steatosis and obesity.^7–8 The silencing of hepatic MGAT1 resulted in a dramatic improvement in blood glucose levels and hepatic steatosis.^7–8 In addition, there was evidence suggesting that MGAT2 and MGAT3 were overexpressed in the livers of patients with nonalcoholic fatty liver disease (NAFLD). ¹¹ JTP-103237, an MGAT2 inhibitor, was shown to prevent fatty liver and suppress both hepatic TG synthesis and de novo lipogenesis in a carbohydrate-induced mouse fatty liver model. ¹² In that report, the inhibition of hepatic MGAT activity by JTP-103237 was assessed using 2-oleoyl and [1-¹⁴C]-oleoyl-CoA as substrates. The radioactivity of the MGAT product, [1-¹⁴C] diacylglycerol, was separated using TLC and analyzed as MGAT activity. Because the liver microsomal membrane preparations contain endogenous DGATs, the DGAT activities can further acylate the hepatic MGAT product, [1-¹⁴C] diacylglycerol, to form [1-¹⁴C]-TG. The use of decanoyl-CoA and 1-decanoyl-rac-glycerol in our MGAT LC/MS/MS assay will produce mostly 1,3-didecanoyl-glycerol as a final MGAT-mediated reaction product, which is not susceptible to acylation to TG. Our MGAT LC/MS/MS assay should aid in the evaluation of the regulation of native MGAT activity in these liver tissue preparations.