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Human GPR40, also known as Free Fatty Acid Receptor 1 (FFAR1)

spinqualitylabelsall models hGPR40 Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Background Human G-protein coupled receptor 40 (hGPR40) is a seven helical transmembrane domain receptor for long-chain free fatty acids that stimulates insulin secretion. This enzyme is primarily located in the pancreatic β-cells in the islets of Langerhans, and as such, it has become a target for potential Type II Diabetes treatments. Activation of hGPR40 has been shown to both stimulate insulin secretion and decrease glucose concentration. GPR40 is a member of a group of homologous GPCRs all located on chromosome 19q13.1 including GPR41, 42, and 43. Structure Like most G-protein coupled receptors, hGPR40 contains seven transmembrane helices (top view of TM helices). In order obtain a crystallized structure of the protein, four stabilizing mutations (L42A, F88A, G103A, Y202F) were made to increase expression levels and thermal stability of the protein. Binding Sites Tak-875 Binding Site Figure 1. Second proposed binding site of GPR40. By visual inspection, a second possible binding site was proposed between transmembrane helices 3, 4, and 5 on the intracellular side. Figure 2. Third proposed binding site of GPR40. By visual inspection, a third possible binding site was proposed between transmembrane helices 1, 2, and 7 on the extracellular side. Charge Network hGPR40 has a distinct binding pocket that is established by seven key residues. File:Charge network residues.png Figure 3. TAK-875 binding residues The importance of these residues for agonist binding was determined by mutagenesis studies. Each of these residues have either a charged or polar R-group that allows them to develop a charge network. This network keeps the residues in a stable, unbound state until exposed to a substrate. When the substrate (an agonist) enters the binding pocket, four of the seven Key Binding Residues interact directly with the carboxylate moiety of the agonist. In 2007 and 2009 researchers showed the presence of Arg 183 and Arg 258 in the binding pocket Along with the two Arginine residues, the charge network incorporates two Tyrosine residues.These residues (Tyr 91 and Tyr 240) also stabilize the carboxylate of the agonists. It was further determined that Tyr 240 is epecially important for binding. Mutation of Tyr 240 caused a reduction in the binding affinity of TAK-875 by eight fold and had a significant effect on the Kd of the protein. ECL2 Although it may be different in many ways, hGPR40 is similar to most G protein coupled receptors because it contains a highly conserved hairpin loop. This extracellular loop (ECL2), is accompanied by a disulfide bond and serves an important role in the protein. In hGPR40, ECL2 has two sections: a beta sheet and an auxiliary loop. The beta sheet (shown in cyan) spans helices 4 and 5. hGPR40's ECL2 differs from that of other proteins because it contains an auxiliary loop (magenta) of 13 extra residues. The entire extracellular loop has low mobility and flexibility. The allows it to act as a cap for the binding pocket. The only exception to the low flexibility is the tip of the auxiliary loop, which corresponds to residues Asp 152-Asn 155. This area of greater mobility allows for substrates to enter the binding site. Function Mechanism of Insulin Secretion One proposed pathway of insulin secretion by hGPR40 involves the activation of the Gaq/11 protein complex. This complex then activates phospholipase C (PLC) which in turn phosphorylates phosphatidylinositol 4,5-bisphosphate to inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). IP3 can then mediate the influx of Ca2+ caused by the binding of free fatty acids to hGPR40 by moving into the cytoplasm, binding to the endoplasmic reticulum, and allowing for the release of Ca2+ into the cytosol. This increase in [Ca2+] amplifies the similar increase in [Ca2+] that results from high concentrations of glucose. In this way, hGPR40 mimics glucose dependent insulin secretion. Another pathway through which hGPR40 induces insulin expression is through phospholipase D1 (PKD1). When free fatty acids bind to hGPR40, it is able to phosphorylate and therefore activate PKD1. The PKD1 plays a role in controlling the organization of an actin network that lays in role in insulin secretion. Clinical Relevance By signaling predominantly through Gaq/11, GPR40 increases intracellular calcium and activates phospholipases to generate diacylglycerols resulting in increased insulin secretion. Synthetic small-molecule agonists of GPR40 enhance insulin secretion in a glucosedependent manner in vitro and in vivo with a mechanism similar to that found with fatty acids. GPR40 agonists have shown efficacy in increasing insulin secretion and lowering blood glucose in rodent models of type 2 diabetes. TAK-875 Figure 4. Structure of TAK-875 One example of an hGPR40 agonist is Tak-875. TAK-875 has shown efficacy in increasing insulin secretion and lowering blood glucose in rodent models of type 2 diabetes. This drug was studied in stage III clinical trials and was able to significantly reduce HbA1c and fasting plasma glucose levels in Japanese patients with type 2 diabetes that was not controlled by diet and exercise. However, clinical trials were stopped shortly after this study because TAK-875 was suspected of causing liver damage.