Monoglyceride lipase
From Proteopedia
Monoglyceride Lipase (MGL)
IntroductionMonoglyceride Lipase (MGL, MAGL, MGLL) is a 33 kDa protein [1] found mostly in the cell membrane (). MGL is a serine hydrolase enzyme that contains an α/β hydrolase fold. MGL plays a key role in the hydrolysis of 2-arachidonoylglycerol (2-AG), an endocannabinoid produced by the the central nervous system.[1][2][3][4] The hydrolase fold, along with a characteristic amphipathic occluded tunnel, allows MGL's active site to selectively bind to 2-AG and degrade it into arachidonic acid and glycerol.[2] 2-AG has been found to possess anti-nociceptive, immunomodulatory, anti-inflammatory and tumor-reductive character when it binds to cannabinoid receptors. [1] [2] Due to the vast medical and therapeutic utility of 2-AG, the inhibition of MGL is a high interest target in pharmaceutical research. Furthermore, MGL has also been cited as having both negative and positive effector roles in cancer pathology. [5] [6] 3D StructureThe first complete crystal structure of MGL was determined in 2009 in its apo form. [2] MGL is a part of the α-β hydrolase family of enzymes.[1][2][3] This category of proteins contains an beta sheet, specifically containing seven parallel and one antiparallel constituent strand, by alpha-helices. [2] MGL has a characteristic lid domain comprised of two large loops that surround .[2] This region of the enzyme is the membrane-interacting moiety of the protein, which is consistent with its amphipathic nature and outward-facing (graphite being nonpolar and cyan being highly polar). 2-AG and other lipids suspended in the hydrophobic section of the cell membrane have been proposed to associate with this region of MGL before entering the active tunnel.[2] Interestingly, MGL’s lid domain may be more flexible than its analogs in other α-β hydrolases, due to the various conformations it assumed in crystallographic studies. [2] Currently, there is no consensus regarding the quaternary arrangement of MGL. Some studies show that MGL is primarily found as a monomer, [2] [3] whereas other studies have found it to be a physiologically active . [1] One compelling piece of evidence for the dimeric quartenary structure is the presence of a pair of beta strands between the two molecules of MGL in 3JW8. Active SiteMGL contains an active site roughly 25Å long and 8Å wide residing beneath its lid region. Like its substrates, 2-AG and other monoacylglycerols, the tunnel is largely amphipathic. Hydrophobic residues dominate the tunnel with the exception of the terminal occluded region, which houses the catalytic triad. In its apo form, the catalytic region is not solvent-exposed, unlike the wide opening of the tunnel. [1][2] A unique structural motif in MGL is a 5Å solvent-exposed hole connecting the exterior to the catalytic site. This structure is proposed to act as an “exit hole” through which the glycerol product leaves MGL. The fatty acid product, namely arachidonic acid, presumably travels back through the active site tunnel. [1][2][3] Catalytic TriadMGL’s serine hydrolase chemistry is executed by a (Ser132-His279-Asp249) and seems to utilize the same mechanism as the much-studied chymotrypsin. In this mechanism, an activated serine nucleophile cleaves the ester bond of the substrate.[1][2][3] The subsequent tetrahedral intermediate is stabilized by the , formed by the main-chain nitrogens of Ala61 and Met (or Se-Met) 133.[2] Biological/Medical RelevanceMonoglyceride Lipase is involved in energy metabolism through two mechanisms. In the first mechanism, MGL hydrolyzes monoacylglycerols into fatty acids and glycerol, which are able to then be used for energy production [7]. The second mechanism involves the degradation of 2-arachidonoyl glycerol (2-AG), which is a common endogenous ligand of cannabinoid receptors, by MGL. 2-AG Metabolism2-AG activates the same cannabinoid receptors (CB1 and CB2) for both anandamide and the main psychoactive compound found in Cannabis sativa, Δ9-Tetrahydrocannabinol (THC), via retrograde signaling. [2][1] In the brain, endocannabinoids (ECs) are released from postsynaptic neurons, causing the retrograde suppression of synaptic transmission. [7] In peripheral tissues, endocannabinoids (ECs) are active in autonomic nervous system. EC signalling affects processes such as learning, motor control, cognition, and pain [7]. EC signalling is also able to regulate lipid metabolism and food intake. 2-AG is the most abundant endocannabinoid found in the brain, possessing analgesic, anti-inflammatory, immunomodulating, neuroprotective, and hypotensive effects.[1][5] MGL degrades 2-AG, preventing 2-AG from remaining bound to the cannabinoid receptor and therefore terminating the pain signal. Without the degradation of 2-AG by MGL, 2-AG levels would increase which would lead to a prolonged nociceptive effect [8] Approximately 85% of the 2-AG in the rat brain is metabolized by MGL, while other lipases such as fatty acid amide hydrolase (FAAH) process the remainder of the metabolite.[4] Based on these studies, MGL has been assigned as the primary enzyme for the metabolism of 2-AG in humans, making it a highly desirable target enzyme for the modulation of 2-AG concentration in the body. [1][2][3] A deficiency in MGL in animals led to the buildup of 2-AG [7]. The endocannabinoid 2-AG has a nociceptive effect in pain signalling [8]. Although the most-studied role of MGL is the degradation of 2-AG in the brain, MGL may also play a role in adipose tissue, completing the hydrolysis of triglycerides into fatty acids and glycerol, as well as working in the liver to mobilize triglycerides for secretion. [1][3] MGL InhibitorsThree general MGL inhibitor classes have been observed: noncompetitive, partially irreversible inhibitors such as URB602; cysteine-reactive inhibitors such as N-arachidonoylmaleimide (NAM); and irreversible serine-reactive inhibitors such as JZL184 and .[2] SAR629 covalently binds to the catalytic Serine-132; the oxygen of the nucleophilic serene residue attacks the carbonyl carbon of SAR629, forming a carbamate. This covalent bond is believed to be reversible via hydrolysis, albeit slowly.[2] Due to JZL184's similar structure to SAR629, it may undergo a similar reaction with MGL.[2] Despite the existence of multiple lead compounds, there is a strong demand for the creation of more highly-specific and more potent inhibitors that could be used as anti-pain drugs for their ability to keep 2-AG active in the neuronal synapses. [1] Cancer RelevanceMGL is also a target for continuing cancer research, with the potential to help distinguish the role of fatty acids in malignancy. Also of interest is the varying efficacy of endocannabinoids as anti-cancer agents in different body tissues and the multifarious influences on the PI-3k/Akt signaling pathway in carcinogenesis. [6] MGL exerts a twofold influence on cancer growth; endocannabinoids such as 2-AG have been shown to have anti-tumorigenic properties [1] [5] and a high fatty-acid concentration may play a role in the promotion of cancer aggressiveness and malignancy. In aggressive breast, melanoma, ovarian, and prostate cancer cells, MGL activity was found to be higher than in nonaggressive malignant cells.[5] Subsequently, the creation of effective MGL inhibitors may help to treat highly aggressive cancers in addition to their proposed use as analgesics. Recent evidence, however, has suggested that in lung, breast, ovary, stomach, and colorectal cancer, MGL expression was reduced. In addition to controlling 2-AG degradation and fatty acid synthesis pathways, MGL also interacts with key phospholipids (specifically, the 3-phosphorylated phosphoinositide products of PI-3K) in the PI3K/Akt signaling and tumor growth pathway. MGL serves as a negative effector in the pathway: as the concentration of MGL decreases, Akt phosphorylation increases. [6] MGL’s role in different body tissues is an ongoing area of research aimed at elucidating its complex role in cancer pathology. MGL’s effect on exogenous cannabinoid medications that are administered to cancer patients as a palliative medication is of particular scientific interes. [5]
Inhibition of MGLThe importance of Inhibition of Monoglyceride lipase is to keep it from breaking down 2-arachidonoyl glycerol. When 2-Ag is broken down it is not able to suppress pain and depression brain functions that human beings experience. N-arachidonyl maleimide (NAM) is one inhibitor of MGL that reacts with the amino acid . Figure 2  This Cysteine is buried in the active site near the catalytic serine and functions by sterically clashing with the natural ligand. A possible conformational change to Cys252 upon the binding of NAM could also lead to an inactive form of MGL. MGL is also inhibited by being in complex with that is covalently bound to the catalytic Ser132. SAR629 adopts a Y shape and interacts with the MGL by hydrophobic interactions, with a few polar interactions as well. Figure 3  With SAR629 interacting with the catalytic triad it inhibits the triad from breaking down 2-AG and inactivates MGL [9] StructureThe of MGL has an eight-stranded β-sheet protein fold with seven parallel and one . Similar to the other α/β hydrolases, the β-sheets in the center of the protein surrounded by α-helices. The combination of the α-helices and β-sheets are able to provide a stable scaffold for the active site within MGL. MGL is monomeric. The catalytic triad, containing Ser132, His279, and Asp249, is found at the bottom of the binding pocket [9]. Catalytic triadMGL has a classic that contains Ser-His-Asp. The triad was found using site-directed mutagenesis of each individual residue and each of these amino acid residues are catalytically essential to MGL [9]. The catalytic triad is located in the Binding Pocket buried at the bottom of it in the oxyanion hole connected by a water molecule.Figure 4  This triad has a natural attraction to Endocannabinoids, specifically 2-arachidonylglycerol (2-AG) [9]. Binding2-AG binds to the catalytic triad and is hydrolyzed. The structure of 2-AG contains a long and flexible aliphatic chain and a polar head that is cleaved. It is the polar head that gets attracted to the catalytic triad and binds to it so the catalytic Serine can cleave 2-AG. 2-AG is broken down into arachidonic acid and glycerol which makes 2-AG inactive[9]. See Overall Reaction. Inhibition of Catalytic TriadResearch on MGL is being geared towards inhibiting 2-AG from binding to the catalytic triad and being hydrolyzed. The binding of 2-AG to the catalytic triad can be extracted before being hydrolyzed. MPD (2-methyl-pentane-2,4-diol)is located at the end of the tunnel where the catalytic triad is at and the tunnel is filled with MPD molecules. MPD being in the same vicinity will extract 2-AG from the triad and the MPD molecule will sit in there in place of 2-AG. This is a natural inhibition phenomenon. Inhibition of MGL leads to increase in 2-AG levels since AG is broken down by MGL [8]. The catalytic triad is a major part of MGL and its interaction with other parts within the brain and how the brain functions. Overall Reaction In this reaction 2-AG binds to the catalytic triad in the oxyanion hole in the active site. In the oxyanion holes the substrate is stabilized by two nitrogen atoms from the catalytic Histidine and Aspartate during the transition step of the catalytic reaction. The catalytic triad activates the nucleophilic serine and cleaves the ester bond of 2-AG that is being stabilized by its carbonyl group that is attached to the oxyanion hole. The glycerol molecule is released and it might diffuse to the narrow "exit hole", while the arachidonic acid would diffuse back to the top of the tunnel and leave the protein [9]. Ligand Binding Site  The of MGL has a large hydrophobic region with a polar bottom. The entrance of the binding pocket for MGL contains a lid, which is very flexible [9]. The binding pocket or tunnel within MGL matches with the overall structure of 2-AG, with 2-AG's polar head being cleaved by the catalytic triad Figure 7. The binding pocket is not being adjusted to the ligand's shape. However, the main movements of MGL involve the lid region of the ligand binding pocket upon the ligand binding. When 2-AG and its isomer 1(3)-AG bind to MGL, the hydrophobic chain is first aligned with the left part of the binding pocket. The carbonyl on 2-AG and 1(3)-AG is then hydrogen bonded to . The polar head group of the ligand is then fixed by three hydrogen bonds. The large lipophilic portion of the binding pocket is being used to design more selectivie inhibitors [9]. References
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