Opioid receptors

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**[[Mu Opioid Receptor Bound to a Morphinan Antagonist]]
**[[Mu Opioid Receptor Bound to a Morphinan Antagonist]]
**[[μ Opioid Receptors]]
**[[μ Opioid Receptors]]
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**[[Mu Opioid Receptor]].
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**[[Mu Opioid Receptor]]
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The binding of an opioid induces a <scene name='78/786661/Mor_on_off/2'>conformational change</scene> in the μ-opioid receptor that activates an inhibitory G-protein (Gαi/o). This results in the dissociation of the G-protein complex. The Gα subunit then inhibits adenylyl cyclase. The Gβγ subunit acts to inhibit Ca2+ channels and activate K+ channels. <scene name='87/874998/Mor_on_off/1'>Activation mechanism</scene>.
**[[6dde]] μ-opioid receptor: G protein complex<br />
**[[6dde]] μ-opioid receptor: G protein complex<br />
* The '''κ-opioid receptor''' binds opium-type ligands. For details see [[Student Project 3 for UMass Chemistry 423 Spring 2015]].<br />
* The '''κ-opioid receptor''' binds opium-type ligands. For details see [[Student Project 3 for UMass Chemistry 423 Spring 2015]].<br />
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The κ-opioid receptor is a <scene name='48/483884/K_or_general/1'>homodimer</scene>. The extracellular side is home to the proteins primary <scene name='48/483884/K_or_binding_general/2'>active site</scene>. These 2 units will span the length for the cell membrane to form the basis of the receptor molecule. <scene name='48/483884/K_or_dimmer_assembly/1'>The each subunit is attached to the other by the I, II and VIII α-helices</scene>, where helices I (in light blue) and helices VIII (in dark blue). This area will make up the basis for the intermembrane surface area. A distinguishing feature that separates the κ-opioid receptor from other receptors, is the large β-hairpin, <scene name='48/483884/K_or_beta_sheet/3'>ECL2</scene>, located near the main active site of the protein. It is believed that its function is to cap the active site of the receptor. Although in general, this protein is primarily composed of α-helices, not β-sheets (Compare <scene name='48/483884/K_or_beta_sheet/1'>β-sheet</scene> to <scene name='48/483884/K_or_alpha/1'>α-helices</scene>). This evidence reinforces the idea that this protein is a transmembrane protein rather than one found inside the cytosol. In general transmembrane protein are composed almost entirely of α-helices (or β-sheet arranged in special fashion called a β-barrel), in order to have maximum stability inside the membrane. Interesting feature of the κ-opioid receptor is the <scene name='48/483884/K_or_disulfide_bond/1'>disulfide bond </scene> formed by Cys131 and Cys210 which is conserved across all opioid receptors. <scene name='48/483884/K_or_ligand_biding_pocket_asp/1'>Active site</scene> of κ-opioid receptor. The human κ-opioid receptor ligand binding pocket displays a unique combination of key characteristics both shared with and distinct from those in the chemokine and aminergic receptor families.
* The '''δ-opioid receptor''' binds enkephalins. For details see [[Delta opioid receptor]].
* The '''δ-opioid receptor''' binds enkephalins. For details see [[Delta opioid receptor]].
* The '''Nociceptin/orphanin FQ opioid receptor''' binds the heptadecapeptide orphanin<ref>PMID:23395957</ref>.
* The '''Nociceptin/orphanin FQ opioid receptor''' binds the heptadecapeptide orphanin<ref>PMID:23395957</ref>.

Revision as of 12:49, 24 May 2021

Structure of κ-opioid receptor complex with opioid antagonist, citric acid, PEG and octadec-enoate derivative (PDB entry 4djh)

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References

  1. Feng Y, He X, Yang Y, Chao D, Lazarus LH, Xia Y. Current research on opioid receptor function. Curr Drug Targets. 2012 Feb;13(2):230-46. PMID:22204322
  2. Donica CL, Awwad HO, Thakker DR, Standifer KM. Cellular mechanisms of nociceptin/orphanin FQ (N/OFQ) peptide (NOP) receptor regulation and heterologous regulation by N/OFQ. Mol Pharmacol. 2013 May;83(5):907-18. doi: 10.1124/mol.112.084632. Epub 2013 Feb , 8. PMID:23395957 doi:http://dx.doi.org/10.1124/mol.112.084632

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Alexander Berchansky, Michal Harel

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