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Human metabotropic glutamate receptor 5 transmembrane domain

spinqualitylabelsall models Human metabotropic glutamate receptor 5 transmembrane domain Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Receiving and responding to extracellular messages is critical to the proper function of the nervous system. Glutamate is the major excitory neurotransmitter of the CNS, and metabotropic glutamate receptor 5 will play a major role in glutamate signaling. Metabotropic glutamate receptor 5 transmembrane domain is a homodimeric GPCR that resides in the cellular membrane . This domain is a member of the Class C GPCR family and can further be categorized into the Group I subgroup. The transmembrane domain will signal through a Gq/11 pathway. mGlu5 will bind glutamate to the extracellular Venus flytrap domain and the signal will be transduced across the membrane to a heterotrimeric G protein, which will ultimately lead to calcium release and activation of PKC. This will elicit a excitory post-synaptic repose and modulate long term potentiation. Human metabotropic glutamate receptor 5 is found throughout the central nervous system. Areas containing high concentrations of this protein are often involved involved in emotions and higher cognition. The localization of mGlu5 in the CNS and the presence of multiple domains makes mGlu5 a possible target for treating schizophrenia,Fragile X, depression, anxiety,and Alzheimer's disease. Discovery The mGlu family of receptors was the first of the Class C GPCR to be extensively studied. The first regions of the protein crystallized and studied were the Venus fly trap domain and the cystiene-rich domain on the extracellular region of the receptor. The hydrophobic nature and flexibility of the transmembrane domain made it difficult to crystallize. Recently, the human metabotropic glutamate receptor 5 transmembrane domain was crystallized and a structure elucidated. There were several modifications that had to be made to the TMD for it to successfully crystallize. The protein was thermostabilized and flexible domains were removed. In total residue 2-568 and residues 837-1153 were excised from the structure. Also, a T4 -Lysozyme was inserted into ICL-2. Structure Overall Structure of the TMD. The polar heads on the Oliec acids orient the protein with the top of the image being the extracellular portion of the protein,the middle portion inserted into the membrane, and the lower portion located inside of the cell. Overview The mGlu5 TMD contains 7 alpha helices that span the membrane. The protein was crystallized with Oleic acid and MES. On the superior portion of the protein there are several critical extracellular loops.The binding pocket can be found near the middle of the protein.Inserted into the biding pocket is the negative allosteric modulator mavoglurant. It is important to note that the TMD as illustrated is in an inactive conformation. On the intracellular portion of the protein there exist several ionic locks whose positions will determine the activity of the protein. Binding Pocket The binding pocket represents an interesting source of regulatory control of receptor activity. The binding pocket is only accessible by a relatively narrow (7 angstrom) entrance. This small entrance severely restricts the access of both positive and negative allosteric regulators. This structural feature will severely limit the size of possible regulators. Important Amino Acids: Asparagine 747forms a hydrogen bond network with main chain carbonyl of 652 and the carbamate portion of mavoglurant. Bicyclic ring surrounded by hydrophobic binding pocket. 2 Catalytic serine resides H-bond to the hyrdoxyl oxygen of our ligand. A water molecular inside of the binding pocket helps stabilize the inactive state. Once bound to mavoglurant, transmembrane helix 7 undergoes a conformational change. The shifting of TM7 will lead to a more global conformational change, which we leave the receptor incapable of signaling. Ionic Locks Another important structural feature of the protein is the series of ionic locks on the intracellular side of the protein. Interaction between amino acids will form a salt bridge which will stabilize the inactive conformation. The primary ionic lock forms between Glu770, Lys665, and Ser613. A secondary ionic lock occurs between Ser614 and Arg668. The purpose of these ionic locks are analogous to the ionic interactions that stabilize the T state in Hemoglobin. In the case of the TMD, when the NAM mavoglurant is bound the ionic lock is formed. This stabilizes the inactive state, where the intracellular loops are stabilized inwards. This will effectively block the crevice that is involved in binding the G-protien. Models have suggested that, even in a glutamate bound state, the mavoglurant bound receptor would be dimerized but incapable of signaling. This helps maintain the readiness of the pathway, while still decreasing signal response. Disease Fragile X Fragile X syndrome is the most common genetic cause of mental disabilty, and is a member of the Autism spectrum disorder family. The severity of intellectual disability can vary from patient to patient, but symptoms stem from a misregulation of the mGlu1 and MGlu5 pathways. This leads to over potentiation in neural cells. Mavoglurant and other allosteric regulators like fenobam have shown promise in treating Fragile X.One positive characteristic of ligands that target the TMD is they tend to be more specific, thus interacting less with brain proteins. Mavoglurant would act to down regulate glutamate signaling in an attempt to decrease potentiation. Unfortunately, recent Phase 2 clinical trials have proven mavoglurant ineffective . Novartis the company who developed the drug has stopped clinical trials of mavoglurant . However, modulators of mGlu5 TMD are still be researched to treat Parkinson's, Alzheimer's disease, and various addictions. Structural highlights TextToBeDisplayed 7 Helices This is a sample scene created with SAT to color by Group, and another to make a transparent representation of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes. TextToBeDisplayed

External Resources

Novartis Fragile X trials