메뉴 건너뛰기




Volumn 170, Issue 3, 2017, Pages 414-427

How Ligands Illuminate GPCR Molecular Pharmacology

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA 1 ADRENERGIC RECEPTOR BLOCKING AGENT; ANGIOTENSIN RECEPTOR ANTAGONIST; ATYPICAL ANTIPSYCHOTIC AGENT; BETA 2 ADRENERGIC RECEPTOR STIMULATING AGENT; CHOLINERGIC RECEPTOR BLOCKING AGENT; CINACALCET; DOPAMINE 2 RECEPTOR BLOCKING AGENT; G PROTEIN COUPLED RECEPTOR; HISTAMINE H1 RECEPTOR ANTAGONIST; MARAVIROC; OPIATE; SEROTONIN 1D AGONIST; SONIDEGIB; VISMODEGIB; LIGAND;

EID: 85026367955     PISSN: 00928674     EISSN: 10974172     Source Type: Journal    
DOI: 10.1016/j.cell.2017.07.009     Document Type: Review
Times cited : (410)

References (111)
  • 1
    • 65549086510 scopus 로고    scopus 로고
    • Temporally precise in vivo control of intracellular signalling
    • Airan, R.D., Thompson, K.R., Fenno, L.E., Bernstein, H., Deisseroth, K., Temporally precise in vivo control of intracellular signalling. Nature 458 (2009), 1025–1029.
    • (2009) Nature , vol.458 , pp. 1025-1029
    • Airan, R.D.1    Thompson, K.R.2    Fenno, L.E.3    Bernstein, H.4    Deisseroth, K.5
  • 2
    • 59449104972 scopus 로고    scopus 로고
    • Prescription drug spending trends in the United States: looking beyond the turning point
    • Aitken, M., Berndt, E.R., Cutler, D.M., Prescription drug spending trends in the United States: looking beyond the turning point. Health Aff. (Millwood) 28 (2009), w151–w160.
    • (2009) Health Aff. (Millwood) , vol.28 , pp. w151-w160
    • Aitken, M.1    Berndt, E.R.2    Cutler, D.M.3
  • 4
    • 79951512210 scopus 로고    scopus 로고
    • Strategies to discover unexpected targets for drugs active at G protein-coupled receptors
    • Allen, J.A., Roth, B.L., Strategies to discover unexpected targets for drugs active at G protein-coupled receptors. Annu. Rev. Pharmacol. Toxicol. 51 (2011), 117–144.
    • (2011) Annu. Rev. Pharmacol. Toxicol. , vol.51 , pp. 117-144
    • Allen, J.A.1    Roth, B.L.2
  • 6
    • 0031032769 scopus 로고    scopus 로고
    • Human herpesvirus KSHV encodes a constitutively active G-protein-coupled receptor linked to cell proliferation
    • Arvanitakis, L., Geras-Raaka, E., Varma, A., Gershengorn, M.C., Cesarman, E., Human herpesvirus KSHV encodes a constitutively active G-protein-coupled receptor linked to cell proliferation. Nature 385 (1997), 347–350.
    • (1997) Nature , vol.385 , pp. 347-350
    • Arvanitakis, L.1    Geras-Raaka, E.2    Varma, A.3    Gershengorn, M.C.4    Cesarman, E.5
  • 7
    • 0021194782 scopus 로고
    • Activation of the inhibitory GTP-binding protein of adenylate cyclase, Gi, by beta-adrenergic receptors in reconstituted phospholipid vesicles
    • Asano, T., Katada, T., Gilman, A.G., Ross, E.M., Activation of the inhibitory GTP-binding protein of adenylate cyclase, Gi, by beta-adrenergic receptors in reconstituted phospholipid vesicles. J. Biol. Chem. 259 (1984), 9351–9354.
    • (1984) J. Biol. Chem. , vol.259 , pp. 9351-9354
    • Asano, T.1    Katada, T.2    Gilman, A.G.3    Ross, E.M.4
  • 8
    • 0024412926 scopus 로고
    • Beta-adrenergic receptor kinase: primary structure delineates a multigene family
    • Benovic, J.L., DeBlasi, A., Stone, W.C., Caron, M.G., Lefkowitz, R.J., Beta-adrenergic receptor kinase: primary structure delineates a multigene family. Science 246 (1989), 235–240.
    • (1989) Science , vol.246 , pp. 235-240
    • Benovic, J.L.1    DeBlasi, A.2    Stone, W.C.3    Caron, M.G.4    Lefkowitz, R.J.5
  • 9
    • 0021058380 scopus 로고
    • Operational models of pharmacological agonism
    • Black, J.W., Leff, P., Operational models of pharmacological agonism. Proc. R. Soc. Lond. B Biol. Sci. 220 (1983), 141–162.
    • (1983) Proc. R. Soc. Lond. B Biol. Sci. , vol.220 , pp. 141-162
    • Black, J.W.1    Leff, P.2
  • 11
    • 0035206793 scopus 로고    scopus 로고
    • Amphetamine, 3,4-methylenedioxymethamphetamine, lysergic acid diethylamide, and metabolites of the catecholamine neurotransmitters are agonists of a rat trace amine receptor
    • Bunzow, J.R., Sonders, M.S., Arttamangkul, S., Harrison, L.M., Zhang, G., Quigley, D.I., Darland, T., Suchland, K.L., Pasumamula, S., Kennedy, J.L., et al. Amphetamine, 3,4-methylenedioxymethamphetamine, lysergic acid diethylamide, and metabolites of the catecholamine neurotransmitters are agonists of a rat trace amine receptor. Mol. Pharmacol. 60 (2001), 1181–1188.
    • (2001) Mol. Pharmacol. , vol.60 , pp. 1181-1188
    • Bunzow, J.R.1    Sonders, M.S.2    Arttamangkul, S.3    Harrison, L.M.4    Zhang, G.5    Quigley, D.I.6    Darland, T.7    Suchland, K.L.8    Pasumamula, S.9    Kennedy, J.L.10
  • 14
    • 0021193681 scopus 로고
    • The mammalian beta 2-adrenergic receptor: reconstitution of functional interactions between pure receptor and pure stimulatory nucleotide binding protein of the adenylate cyclase system
    • Cerione, R.A., Codina, J., Benovic, J.L., Lefkowitz, R.J., Birnbaumer, L., Caron, M.G., The mammalian beta 2-adrenergic receptor: reconstitution of functional interactions between pure receptor and pure stimulatory nucleotide binding protein of the adenylate cyclase system. Biochemistry 23 (1984), 4519–4525.
    • (1984) Biochemistry , vol.23 , pp. 4519-4525
    • Cerione, R.A.1    Codina, J.2    Benovic, J.L.3    Lefkowitz, R.J.4    Birnbaumer, L.5    Caron, M.G.6
  • 15
    • 84983803055 scopus 로고    scopus 로고
    • Allosteric Modulation as a Unifying Mechanism for Receptor Function and Regulation
    • Changeux, J.P., Christopoulos, A., Allosteric Modulation as a Unifying Mechanism for Receptor Function and Regulation. Cell 166 (2016), 1084–1102.
    • (2016) Cell , vol.166 , pp. 1084-1102
    • Changeux, J.P.1    Christopoulos, A.2
  • 18
    • 84940544977 scopus 로고    scopus 로고
    • Fragment and Structure-Based Drug Discovery for a Class C GPCR: Discovery of the mGlu5 Negative Allosteric Modulator HTL14242 (3-Chloro-5-[6-(5-fluoropyridin-2-yl)pyrimidin-4-yl]benzonitrile)
    • Christopher, J.A., Aves, S.J., Bennett, K.A., Doré, A.S., Errey, J.C., Jazayeri, A., Marshall, F.H., Okrasa, K., Serrano-Vega, M.J., Tehan, B.G., et al. Fragment and Structure-Based Drug Discovery for a Class C GPCR: Discovery of the mGlu5 Negative Allosteric Modulator HTL14242 (3-Chloro-5-[6-(5-fluoropyridin-2-yl)pyrimidin-4-yl]benzonitrile). J. Med. Chem. 58 (2015), 6653–6664.
    • (2015) J. Med. Chem. , vol.58 , pp. 6653-6664
    • Christopher, J.A.1    Aves, S.J.2    Bennett, K.A.3    Doré, A.S.4    Errey, J.C.5    Jazayeri, A.6    Marshall, F.H.7    Okrasa, K.8    Serrano-Vega, M.J.9    Tehan, B.G.10
  • 19
    • 84904301809 scopus 로고    scopus 로고
    • International Union of Basic and Clinical Pharmacology. XC. multisite pharmacology: recommendations for the nomenclature of receptor allosterism and allosteric ligands
    • Christopoulos, A., Changeux, J.P., Catterall, W.A., Fabbro, D., Burris, T.P., Cidlowski, J.A., Olsen, R.W., Peters, J.A., Neubig, R.R., Pin, J.P., et al. International Union of Basic and Clinical Pharmacology. XC. multisite pharmacology: recommendations for the nomenclature of receptor allosterism and allosteric ligands. Pharmacol. Rev. 66 (2014), 918–947.
    • (2014) Pharmacol. Rev. , vol.66 , pp. 918-947
    • Christopoulos, A.1    Changeux, J.P.2    Catterall, W.A.3    Fabbro, D.4    Burris, T.P.5    Cidlowski, J.A.6    Olsen, R.W.7    Peters, J.A.8    Neubig, R.R.9    Pin, J.P.10
  • 20
    • 84944496866 scopus 로고
    • The antagonism of acetyl choline by atropine
    • Clark, A.J., The antagonism of acetyl choline by atropine. J. Physiol. 61 (1926), 547–556.
    • (1926) J. Physiol. , vol.61 , pp. 547-556
    • Clark, A.J.1
  • 22
    • 0032486433 scopus 로고    scopus 로고
    • Teratogen-mediated inhibition of target tissue response to Shh signaling
    • Cooper, M.K., Porter, J.A., Young, K.E., Beachy, P.A., Teratogen-mediated inhibition of target tissue response to Shh signaling. Science 280 (1998), 1603–1607.
    • (1998) Science , vol.280 , pp. 1603-1607
    • Cooper, M.K.1    Porter, J.A.2    Young, K.E.3    Beachy, P.A.4
  • 23
    • 0034648757 scopus 로고    scopus 로고
    • Thrombin signalling and protease-activated receptors
    • Coughlin, S.R., Thrombin signalling and protease-activated receptors. Nature 407 (2000), 258–264.
    • (2000) Nature , vol.407 , pp. 258-264
    • Coughlin, S.R.1
  • 24
    • 0019137579 scopus 로고
    • A ternary complex model explains the agonist-specific binding properties of the adenylate cyclase-coupled beta-adrenergic receptor
    • De Lean, A., Stadel, J.M., Lefkowitz, R.J., A ternary complex model explains the agonist-specific binding properties of the adenylate cyclase-coupled beta-adrenergic receptor. J. Biol. Chem. 255 (1980), 7108–7117.
    • (1980) J. Biol. Chem. , vol.255 , pp. 7108-7117
    • De Lean, A.1    Stadel, J.M.2    Lefkowitz, R.J.3
  • 25
    • 79960382104 scopus 로고    scopus 로고
    • Biased ligands for better cardiovascular drugs: dissecting G-protein-coupled receptor pharmacology
    • DeWire, S.M., Violin, J.D., Biased ligands for better cardiovascular drugs: dissecting G-protein-coupled receptor pharmacology. Circ. Res. 109 (2011), 205–216.
    • (2011) Circ. Res. , vol.109 , pp. 205-216
    • DeWire, S.M.1    Violin, J.D.2
  • 26
    • 84874406899 scopus 로고    scopus 로고
    • A G protein-biased ligand at the μ-opioid receptor is potently analgesic with reduced gastrointestinal and respiratory dysfunction compared with morphine
    • DeWire, S.M., Yamashita, D.S., Rominger, D.H., Liu, G., Cowan, C.L., Graczyk, T.M., Chen, X.T., Pitis, P.M., Gotchev, D., Yuan, C., et al. A G protein-biased ligand at the μ-opioid receptor is potently analgesic with reduced gastrointestinal and respiratory dysfunction compared with morphine. J. Pharmacol. Exp. Ther. 344 (2013), 708–717.
    • (2013) J. Pharmacol. Exp. Ther. , vol.344 , pp. 708-717
    • DeWire, S.M.1    Yamashita, D.S.2    Rominger, D.H.3    Liu, G.4    Cowan, C.L.5    Graczyk, T.M.6    Chen, X.T.7    Pitis, P.M.8    Gotchev, D.9    Yuan, C.10
  • 30
    • 0029907599 scopus 로고    scopus 로고
    • Requirement of rigid-body motion of transmembrane helices for light activation of rhodopsin
    • Farrens, D.L., Altenbach, C., Yang, K., Hubbell, W.L., Khorana, H.G., Requirement of rigid-body motion of transmembrane helices for light activation of rhodopsin. Science 274 (1996), 768–770.
    • (1996) Science , vol.274 , pp. 768-770
    • Farrens, D.L.1    Altenbach, C.2    Yang, K.3    Hubbell, W.L.4    Khorana, H.G.5
  • 32
    • 0038024615 scopus 로고    scopus 로고
    • The G-protein-coupled receptors in the human genome form five main families. Phylogenetic analysis, paralogon groups, and fingerprints
    • Fredriksson, R., Lagerström, M.C., Lundin, L.G., Schiöth, H.B., The G-protein-coupled receptors in the human genome form five main families. Phylogenetic analysis, paralogon groups, and fingerprints. Mol. Pharmacol. 63 (2003), 1256–1272.
    • (2003) Mol. Pharmacol. , vol.63 , pp. 1256-1272
    • Fredriksson, R.1    Lagerström, M.C.2    Lundin, L.G.3    Schiöth, H.B.4
  • 33
    • 84975763644 scopus 로고    scopus 로고
    • Interaction of G protein coupled receptors and cholesterol
    • Gimpl, G., Interaction of G protein coupled receptors and cholesterol. Chem. Phys. Lipids 199 (2016), 61–73.
    • (2016) Chem. Phys. Lipids , vol.199 , pp. 61-73
    • Gimpl, G.1
  • 34
    • 67650753759 scopus 로고    scopus 로고
    • Definition of the G protein-coupled receptor transmembrane bundle binding pocket and calculation of receptor similarities for drug design
    • Gloriam, D.E., Foord, S.M., Blaney, F.E., Garland, S.L., Definition of the G protein-coupled receptor transmembrane bundle binding pocket and calculation of receptor similarities for drug design. J. Med. Chem. 52 (2009), 4429–4442.
    • (2009) J. Med. Chem. , vol.52 , pp. 4429-4442
    • Gloriam, D.E.1    Foord, S.M.2    Blaney, F.E.3    Garland, S.L.4
  • 41
    • 13844312649 scopus 로고    scopus 로고
    • ZINC–a free database of commercially available compounds for virtual screening
    • Irwin, J.J., Shoichet, B.K., ZINC–a free database of commercially available compounds for virtual screening. J. Chem. Inf. Model. 45 (2005), 177–182.
    • (2005) J. Chem. Inf. Model. , vol.45 , pp. 177-182
    • Irwin, J.J.1    Shoichet, B.K.2
  • 44
    • 84872221774 scopus 로고    scopus 로고
    • Structure-function of the G protein-coupled receptor superfamily
    • Katritch, V., Cherezov, V., Stevens, R.C., Structure-function of the G protein-coupled receptor superfamily. Annu. Rev. Pharmacol. Toxicol. 53 (2013), 531–556.
    • (2013) Annu. Rev. Pharmacol. Toxicol. , vol.53 , pp. 531-556
    • Katritch, V.1    Cherezov, V.2    Stevens, R.C.3
  • 47
    • 0024446412 scopus 로고
    • Pharmacologic discrimination between receptor heterogeneity and allosteric interaction: resultant analysis of gallamine and pirenzepine antagonism of muscarinic responses in rat trachea
    • Kenakin, T., Boselli, C., Pharmacologic discrimination between receptor heterogeneity and allosteric interaction: resultant analysis of gallamine and pirenzepine antagonism of muscarinic responses in rat trachea. J. Pharmacol. Exp. Ther. 250 (1989), 944–952.
    • (1989) J. Pharmacol. Exp. Ther. , vol.250 , pp. 944-952
    • Kenakin, T.1    Boselli, C.2
  • 55
    • 0030824653 scopus 로고    scopus 로고
    • Three allosteric modulators act at a common site, distinct from that of competitive antagonists, at muscarinic acetylcholine M2 receptors
    • Lanzafame, A., Christopoulos, A., Mitchelson, F., Three allosteric modulators act at a common site, distinct from that of competitive antagonists, at muscarinic acetylcholine M2 receptors. J. Pharmacol. Exp. Ther. 282 (1997), 278–285.
    • (1997) J. Pharmacol. Exp. Ther. , vol.282 , pp. 278-285
    • Lanzafame, A.1    Christopoulos, A.2    Mitchelson, F.3
  • 56
    • 79959564813 scopus 로고    scopus 로고
    • Agonist-bound adenosine A2A receptor structures reveal common features of GPCR activation
    • Lebon, G., Warne, T., Edwards, P.C., Bennett, K., Langmead, C.J., Leslie, A.G., Tate, C.G., Agonist-bound adenosine A2A receptor structures reveal common features of GPCR activation. Nature 474 (2011), 521–525.
    • (2011) Nature , vol.474 , pp. 521-525
    • Lebon, G.1    Warne, T.2    Edwards, P.C.3    Bennett, K.4    Langmead, C.J.5    Leslie, A.G.6    Tate, C.G.7
  • 57
    • 17644402459 scopus 로고    scopus 로고
    • Transduction of receptor signals by beta-arrestins
    • Lefkowitz, R.J., Shenoy, S.K., Transduction of receptor signals by beta-arrestins. Science 308 (2005), 512–517.
    • (2005) Science , vol.308 , pp. 512-517
    • Lefkowitz, R.J.1    Shenoy, S.K.2
  • 59
    • 84862776738 scopus 로고    scopus 로고
    • Biased signaling pathways in β2-adrenergic receptor characterized by 19F-NMR
    • Liu, J.J., Horst, R., Katritch, V., Stevens, R.C., Wüthrich, K., Biased signaling pathways in β2-adrenergic receptor characterized by 19F-NMR. Science 335 (2012), 1106–1110.
    • (2012) Science , vol.335 , pp. 1106-1110
    • Liu, J.J.1    Horst, R.2    Katritch, V.3    Stevens, R.C.4    Wüthrich, K.5
  • 61
    • 0025352299 scopus 로고
    • beta-Arrestin: a protein that regulates beta-adrenergic receptor function
    • Lohse, M.J., Benovic, J.L., Codina, J., Caron, M.G., Lefkowitz, R.J., beta-Arrestin: a protein that regulates beta-adrenergic receptor function. Science 248 (1990), 1547–1550.
    • (1990) Science , vol.248 , pp. 1547-1550
    • Lohse, M.J.1    Benovic, J.L.2    Codina, J.3    Caron, M.G.4    Lefkowitz, R.J.5
  • 65
    • 84860505658 scopus 로고    scopus 로고
    • New insights from structural biology into the druggability of G protein-coupled receptors
    • Mason, J.S., Bortolato, A., Congreve, M., Marshall, F.H., New insights from structural biology into the druggability of G protein-coupled receptors. Trends Pharmacol. Sci. 33 (2012), 249–260.
    • (2012) Trends Pharmacol. Sci. , vol.33 , pp. 249-260
    • Mason, J.S.1    Bortolato, A.2    Congreve, M.3    Marshall, F.H.4
  • 66
    • 79959623775 scopus 로고    scopus 로고
    • 1 rhodopsin mutations in congenital night blindness
    • McAlear, S.D., Kraft, T.W., Gross, A.K., 1 rhodopsin mutations in congenital night blindness. Adv. Exp. Med. Biol. 664 (2010), 263–272.
    • (2010) Adv. Exp. Med. Biol. , vol.664 , pp. 263-272
    • McAlear, S.D.1    Kraft, T.W.2    Gross, A.K.3
  • 70
    • 1642323740 scopus 로고    scopus 로고
    • Protein kinase inhibitors: insights into drug design from structure
    • Noble, M.E., Endicott, J.A., Johnson, L.N., Protein kinase inhibitors: insights into drug design from structure. Science 303 (2004), 1800–1805.
    • (2004) Science , vol.303 , pp. 1800-1805
    • Noble, M.E.1    Endicott, J.A.2    Johnson, L.N.3
  • 71
    • 29444446964 scopus 로고    scopus 로고
    • Heterotrimeric G proteins precouple with G protein-coupled receptors in living cells
    • Nobles, M., Benians, A., Tinker, A., Heterotrimeric G proteins precouple with G protein-coupled receptors in living cells. Proc. Natl. Acad. Sci. USA 102 (2005), 18706–18711.
    • (2005) Proc. Natl. Acad. Sci. USA , vol.102 , pp. 18706-18711
    • Nobles, M.1    Benians, A.2    Tinker, A.3
  • 76
    • 0026937176 scopus 로고
    • Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus
    • Pan, Y., Metzenberg, A., Das, S., Jing, B., Gitschier, J., Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus. Nat. Genet. 2 (1992), 103–106.
    • (1992) Nat. Genet. , vol.2 , pp. 103-106
    • Pan, Y.1    Metzenberg, A.2    Das, S.3    Jing, B.4    Gitschier, J.5
  • 81
    • 84886947656 scopus 로고    scopus 로고
    • Adrenaline-activated structure of β2-adrenoceptor stabilized by an engineered nanobody
    • Ring, A.M., Manglik, A., Kruse, A.C., Enos, M.D., Weis, W.I., Garcia, K.C., Kobilka, B.K., Adrenaline-activated structure of β2-adrenoceptor stabilized by an engineered nanobody. Nature 502 (2013), 575–579.
    • (2013) Nature , vol.502 , pp. 575-579
    • Ring, A.M.1    Manglik, A.2    Kruse, A.C.3    Enos, M.D.4    Weis, W.I.5    Garcia, K.C.6    Kobilka, B.K.7
  • 82
    • 33846017361 scopus 로고    scopus 로고
    • Drugs and valvular heart disease
    • Roth, B.L., Drugs and valvular heart disease. N. Engl. J. Med. 356 (2007), 6–9.
    • (2007) N. Engl. J. Med. , vol.356 , pp. 6-9
    • Roth, B.L.1
  • 83
    • 84958212495 scopus 로고    scopus 로고
    • DREADDs for Neuroscientists
    • Roth, B.L., DREADDs for Neuroscientists. Neuron 89 (2016), 683–694.
    • (2016) Neuron , vol.89 , pp. 683-694
    • Roth, B.L.1
  • 84
    • 84939151970 scopus 로고    scopus 로고
    • Integrated Approaches for Genome-wide Interrogation of the Druggable Non-olfactory G Protein-coupled Receptor Superfamily
    • Roth, B.L., Kroeze, W.K., Integrated Approaches for Genome-wide Interrogation of the Druggable Non-olfactory G Protein-coupled Receptor Superfamily. J. Biol. Chem. 290 (2015), 19471–19477.
    • (2015) J. Biol. Chem. , vol.290 , pp. 19471-19477
    • Roth, B.L.1    Kroeze, W.K.2
  • 86
    • 4644271084 scopus 로고    scopus 로고
    • Magic shotguns versus magic bullets: selectively non-selective drugs for mood disorders and schizophrenia
    • Roth, B.L., Sheffler, D.J., Kroeze, W.K., Magic shotguns versus magic bullets: selectively non-selective drugs for mood disorders and schizophrenia. Nat. Rev. Drug Discov. 3 (2004), 353–359.
    • (2004) Nat. Rev. Drug Discov. , vol.3 , pp. 353-359
    • Roth, B.L.1    Sheffler, D.J.2    Kroeze, W.K.3
  • 87
    • 0034610435 scopus 로고    scopus 로고
    • Evidence for possible involvement of 5-HT(2B) receptors in the cardiac valvulopathy associated with fenfluramine and other serotonergic medications
    • Rothman, R.B., Baumann, M.H., Savage, J.E., Rauser, L., McBride, A., Hufeisen, S.J., Roth, B.L., Evidence for possible involvement of 5-HT(2B) receptors in the cardiac valvulopathy associated with fenfluramine and other serotonergic medications. Circulation 102 (2000), 2836–2841.
    • (2000) Circulation , vol.102 , pp. 2836-2841
    • Rothman, R.B.1    Baumann, M.H.2    Savage, J.E.3    Rauser, L.4    McBride, A.5    Hufeisen, S.J.6    Roth, B.L.7
  • 89
    • 0027513982 scopus 로고
    • A mutation-induced activated state of the beta 2-adrenergic receptor. Extending the ternary complex model
    • Samama, P., Cotecchia, S., Costa, T., Lefkowitz, R.J., A mutation-induced activated state of the beta 2-adrenergic receptor. Extending the ternary complex model. J. Biol. Chem. 268 (1993), 4625–4636.
    • (1993) J. Biol. Chem. , vol.268 , pp. 4625-4636
    • Samama, P.1    Cotecchia, S.2    Costa, T.3    Lefkowitz, R.J.4
  • 92
    • 0025834532 scopus 로고
    • Diversity of G proteins in signal transduction
    • Simon, M.I., Strathmann, M.P., Gautam, N., Diversity of G proteins in signal transduction. Science 252 (1991), 802–808.
    • (1991) Science , vol.252 , pp. 802-808
    • Simon, M.I.1    Strathmann, M.P.2    Gautam, N.3
  • 95
    • 84964403986 scopus 로고    scopus 로고
    • Hitchhiking on the heptahelical highway: structure and function of 7TM receptor complexes
    • Tesmer, J.J., Hitchhiking on the heptahelical highway: structure and function of 7TM receptor complexes. Nat. Rev. Mol. Cell Biol. 17 (2016), 439–450.
    • (2016) Nat. Rev. Mol. Cell Biol. , vol.17 , pp. 439-450
    • Tesmer, J.J.1
  • 102
    • 34447649922 scopus 로고    scopus 로고
    • Beta-arrestin-biased ligands at seven-transmembrane receptors
    • Violin, J.D., Lefkowitz, R.J., Beta-arrestin-biased ligands at seven-transmembrane receptors. Trends Pharmacol. Sci. 28 (2007), 416–422.
    • (2007) Trends Pharmacol. Sci. , vol.28 , pp. 416-422
    • Violin, J.D.1    Lefkowitz, R.J.2
  • 103
    • 77955779227 scopus 로고    scopus 로고
    • Conserved binding mode of human beta2 adrenergic receptor inverse agonists and antagonist revealed by X-ray crystallography
    • Wacker, D., Fenalti, G., Brown, M.A., Katritch, V., Abagyan, R., Cherezov, V., Stevens, R.C., Conserved binding mode of human beta2 adrenergic receptor inverse agonists and antagonist revealed by X-ray crystallography. J. Am. Chem. Soc. 132 (2010), 11443–11445.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 11443-11445
    • Wacker, D.1    Fenalti, G.2    Brown, M.A.3    Katritch, V.4    Abagyan, R.5    Cherezov, V.6    Stevens, R.C.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.