Sandbox Reserved 1095

This Sandbox is Reserved from 25/11/2019, through 30/9/2020 for use in the course "Structural Biology" taught by Bruno Kieffer at the University of Strasbourg, ESBS. This reservation includes Sandbox Reserved 1091 through Sandbox Reserved 1115.

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Human Angiotensin Receptor

Angiotensin receptors belong to the G protein coupled receptor (GPCR) family. This is the hormone receptor of the angiotensin II type 1. This is a trans-membrane protein located mainly in heart, brain, liver and kidneys.

spinqualitylabelsall models Human angiotensin receptor Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Functions See also : Angiotensin_II_receptor_type_1 on Wikipedia History Discovery of angiotensin receptors Researchers suspected since 70s the existence of different angiotensin receptors. However, tools to identify those distinct trans-membrane receptors became available ten years later. Receptors binding assays identified angiotensin receptors in vitro using radioactive angiotensin. Results showed several types of angiotensin receptors, found in different tissues. The main receptors are AT1 and AT2 . Nomenclature Three labs discovered in the same time these two angiotensin receptors and proposed their own nomenclature, leading to confusion. To avoid this, a group of researchers met in Baltimore in 1991 to define a coherent nomenclature. Under the presidency of Merlin Bumpus, a common ground has been found and angiotensin receptors have been classified into two groups called AT1 and AT2 receptors. . Recent studies Finally, around 2015, researchers have found the crystal structure of the receptor in complex with its antagonist ZD7155 and with an inverse agonist olmesartan. X-ray cryogenic-crystallography has been used. They have found similar conformation of the receptor when it is linked to the antagonist or to the inverse agonist. They have also found conserved molecular recognition modes. To complete this discovery, they have realized some experiments with mutants to identify the different residues which interact with the ligand. The structure of this protein have also been solved using an other method called serial femtosecond crystallography, corresponding to the proteopedia page 4YAY. Structure (function relationship) Primary and secondary structure Human angiotensin receptor consists in a 376 amino acid string . The protein is composed of 18 alpha helix and 3 beta sheets. Moreover, 7 alpha helix are made of a majority of hydrophobic amino acids. These helix are long enough to cross the membrane and create an hydrophobic domain which is situated into the membrane. The human angiotensin receptor is therefore an alpha helical trans-membrane protein. Since the angiotensin receptor belongs to the GPCRs family, those 7 alpha helix contain 3 extracellular and 3 intracellular loops. Ligand binding pocket In the extracellular environment, there is a beta-hairpin in conjugation with two extracellular disulfure bridges. This structure is responsible for the opening and the locking of the ligand binding pocket . The ligand goes into an hydrophilic pocket created into the membrane thanks to the 7 alpha helix which create a gate between the membrane and the extracellular environment. G protein-binding site When the angiotensin II binds to the angiotensin receptor in the ligand binding pocket, the conformation of the trans-membrane domain changes to create a cytosolic cleft for the binding and activation of G proteins. In this cleft, several conserved residues can be found, which form functional motifs present in all GPCRs . Interaction with drugs Olmesartan anchored to ATR1 by the residues Tyr 35, Trp84 and Arg167. Those three amino acids seem to play an important role in the binding of the drug to AT1R, thanks to the formation of extensive networks of hydrogen bonds and salt bridges with the ligand . Many drugs used to cure diseases linked with the angiotensin receptor contain a tetrazole group. Studies showed that tetrazole plays an important role in the binding with AT1R. Lys 199 : an important role for AngII binding Interaction with other GPCRs It has been discovered that AT1Rs were also able to bind with other GPCRs to form homo- or heterodimers. Those interactions can modify the sensitivity of the receptor, which leads to different physiological and pathological conditions than the GPCR monomer . The most known heterodimers including AT1 receptor are with ß2-adrenergic receptor, the apelin receptor, and AT2 receptor. Those interactions could be facilitated by several transmembrane domains. The oligomeric complexes' formation complicates the understanding of AT1R pharmacology. Application in the therapeutic field Since angiotensin receptor is involved in the renin-angiotenisin system, it represents a target of choice to cure some diseases like hypertension or heart failure. An over-stimulation of this receptor seems to be involved in hypertension, coronary artery disease, cardiac hypertrophy, heart failure, arrhythmia, stroke, diabetic nephropathy and ischemic heart and renal diseases . Several anti-hypertensive drugs are targeting the angiotensin receptor in order to block it. This is the case for drugs called angiotensin receptor blockers (ARBs) like olmesartan, candesartan, and losartan. One of the common characteristic they share is their biphenyl-tetrazole scaffold.