메뉴 건너뛰기




Volumn 117, Issue , 2013, Pages 143-162

Challenges in the development of heteromer-GPCR-based drugs

Author keywords

Cross talk; Drug discovery; Energy landscape; Fingerprint; Heptaspanning; Screening; Arrestin

Indexed keywords

ADENOSINE A1 RECEPTOR; ADENOSINE A2A RECEPTOR; CHEMOKINE RECEPTOR CXCR4; CHEMOKINE RECEPTOR CXCR7; DOPAMINE 1 RECEPTOR; DOPAMINE 2 RECEPTOR; DRUG; G PROTEIN COUPLED RECEPTOR; GUANINE NUCLEOTIDE BINDING PROTEIN; HETERODIMER; POSTSYNAPTIC RECEPTOR;

EID: 84896689116     PISSN: 18771173     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-12-386931-9.00006-4     Document Type: Chapter
Times cited : (7)

References (88)
  • 2
    • 0036209874 scopus 로고    scopus 로고
    • Endocytosis of G protein-coupled receptors: Roles of G protein-coupled receptor kinases and beta-arrestin proteins
    • [Review]
    • A. Claing, S.A. Laporte, M.G. Caron, and R.J. Lefkowitz Endocytosis of G protein-coupled receptors: roles of G protein-coupled receptor kinases and beta-arrestin proteins Prog Neurobiol 66 2002 61 79 [Review]
    • (2002) Prog Neurobiol , vol.66 , pp. 61-79
    • Claing, A.1    Laporte, S.A.2    Caron, M.G.3    Lefkowitz, R.J.4
  • 3
    • 0029963151 scopus 로고    scopus 로고
    • The cluster-arranged cooperative model: A model that accounts for the kinetics of binding to A1 adenosine receptors
    • R. Franco, V. Casadó, F. Ciruela, J. Mallol, C. Lluis, and E.I. Canela The cluster-arranged cooperative model: a model that accounts for the kinetics of binding to A1 adenosine receptors Biochemistry 35 1996 3007 3015
    • (1996) Biochemistry , vol.35 , pp. 3007-3015
    • Franco, R.1    Casadó, V.2    Ciruela, F.3    Mallol, J.4    Lluis, C.5    Canela, E.I.6
  • 4
  • 5
    • 0037445941 scopus 로고    scopus 로고
    • Ligand-induced caveolae-mediated internalization of A(1) adenosine receptors: Morphological evidence of endosomal sorting and receptor recycling
    • M. Escriche, J. Burgueno, F. Ciruela, E.I. Canela, J. Mallol, and C. Enrich Ligand-induced caveolae-mediated internalization of A(1) adenosine receptors: morphological evidence of endosomal sorting and receptor recycling Exp Cell Res 285 2003 72 90
    • (2003) Exp Cell Res , vol.285 , pp. 72-90
    • Escriche, M.1    Burgueno, J.2    Ciruela, F.3    Canela, E.I.4    Mallol, J.5    Enrich, C.6
  • 6
    • 0032503692 scopus 로고    scopus 로고
    • Adenosine deaminase and A1 adenosine receptors internalize together following agonist-induced receptor desensitization
    • C.A. Saura, J. Mallol, E.I. Canela, C. Lluis, and R. Franco Adenosine deaminase and A1 adenosine receptors internalize together following agonist-induced receptor desensitization J Biol Chem 273 1998 17610 17617
    • (1998) J Biol Chem , vol.273 , pp. 17610-17617
    • Saura, C.A.1    Mallol, J.2    Canela, E.I.3    Lluis, C.4    Franco, R.5
  • 7
    • 0033944602 scopus 로고    scopus 로고
    • The heat shock cognate protein hsc73 assembles with A(1) adenosine receptors to form functional modules in the cell membrane
    • S. Sarrió, V. Casadó, M. Escriche, F. Ciruela, J. Mallol, and E.I. Canela The heat shock cognate protein hsc73 assembles with A(1) adenosine receptors to form functional modules in the cell membrane Mol Cell Biol 20 2000 5164 5174
    • (2000) Mol Cell Biol , vol.20 , pp. 5164-5174
    • Sarrió, S.1    Casadó, V.2    Escriche, M.3    Ciruela, F.4    Mallol, J.5    Canela, E.I.6
  • 8
    • 17944383882 scopus 로고    scopus 로고
    • The adenosine A(2A) receptor interacts with the actin-binding protein alpha-actinin
    • J. Burgueño, D.J. Blake, M.A. Benson, C.L. Tinsley, C.T. Esapa, and E.I. Canela The adenosine A(2A) receptor interacts with the actin-binding protein alpha-actinin J Biol Chem 278 2003 37545 37552
    • (2003) J Biol Chem , vol.278 , pp. 37545-37552
    • Burgueño, J.1    Blake, D.J.2    Benson, M.A.3    Tinsley, C.L.4    Esapa, C.T.5    Canela, E.I.6
  • 9
    • 0029892284 scopus 로고    scopus 로고
    • Adenosine deaminase interacts with A(1) adenosine receptors in pig brain cortical membranes
    • C. Saura, F. Ciruela, V. Casado, E.I. Canela, J. Mallol, and C. Lluis Adenosine deaminase interacts with A(1) adenosine receptors in pig brain cortical membranes J Neurochem 66 1996 1675 1682
    • (1996) J Neurochem , vol.66 , pp. 1675-1682
    • Saura, C.1    Ciruela, F.2    Casado, V.3    Canela, E.I.4    Mallol, J.5    Lluis, C.6
  • 11
    • 81155141382 scopus 로고    scopus 로고
    • Visualization and quantification of protein-protein interactions in cells and tissues
    • M. Gullberg, and A.C. Andersson Visualization and quantification of protein-protein interactions in cells and tissues Nat Methods 7 2010 5 6
    • (2010) Nat Methods , vol.7 , pp. 5-6
    • Gullberg, M.1    Andersson, A.C.2
  • 13
    • 0034785580 scopus 로고    scopus 로고
    • Increased AT(1) receptor heterodimers in preeclampsia mediate enhanced angiotensin II responsiveness
    • S. AbdAlla, H. Lother, A. el Massiery, and U. Quitterer Increased AT(1) receptor heterodimers in preeclampsia mediate enhanced angiotensin II responsiveness Nat Med 7 2001 1003 1009
    • (2001) Nat Med , vol.7 , pp. 1003-1009
    • Abdalla, S.1    Lother, H.2    El Massiery, A.3    Quitterer, U.4
  • 15
    • 13544277093 scopus 로고    scopus 로고
    • Regional differences in the prevalence of pre-eclampsia in relation to the risk factors for coronary artery disease in women in Finland
    • R. Kaaja, T. Kinnunen, and R. Luoto Regional differences in the prevalence of pre-eclampsia in relation to the risk factors for coronary artery disease in women in Finland Eur Heart J 26 2005 44 50
    • (2005) Eur Heart J , vol.26 , pp. 44-50
    • Kaaja, R.1    Kinnunen, T.2    Luoto, R.3
  • 16
    • 0034905136 scopus 로고    scopus 로고
    • The prevalence of pre-eclampsia and obstetric outcome in pregnancies of normotensive and hypertensive women attending a hospital specialist clinic
    • C. Lydakis, M. Beevers, D.G. Beevers, and G.Y. Lip The prevalence of pre-eclampsia and obstetric outcome in pregnancies of normotensive and hypertensive women attending a hospital specialist clinic Int J Clin Pract 55 2001 361 367
    • (2001) Int J Clin Pract , vol.55 , pp. 361-367
    • Lydakis, C.1    Beevers, M.2    Beevers, D.G.3    Lip, G.Y.4
  • 17
    • 40349088830 scopus 로고    scopus 로고
    • G-protein-coupled receptor heteromers: Function and ligand pharmacology
    • [Review]
    • R. Franco, V. Casadó, A. Cortés, J. Mallol, F. Ciruela, and S. Ferré G-protein-coupled receptor heteromers: function and ligand pharmacology Br J Pharmacol 153 Suppl. 1 2008 S90 S98 [Review]
    • (2008) Br J Pharmacol , vol.153 , Issue.SUPPL. 1
    • Franco, R.1    Casadó, V.2    Cortés, A.3    Mallol, J.4    Ciruela, F.5    Ferré, S.6
  • 18
    • 80051566993 scopus 로고    scopus 로고
    • Detection of antigen interactions ex vivo by proximity ligation assay: Endogenous dopamine D2-adenosine A2A receptor complexes in the striatum
    • P. Trifilieff, M.L. Rives, E. Urizar, R.A. Piskorowski, H.D. Vishwasrao, and J. Castrillon Detection of antigen interactions ex vivo by proximity ligation assay: endogenous dopamine D2-adenosine A2A receptor complexes in the striatum Biotechniques 51 2011 111 118
    • (2011) Biotechniques , vol.51 , pp. 111-118
    • Trifilieff, P.1    Rives, M.L.2    Urizar, E.3    Piskorowski, R.A.4    Vishwasrao, H.D.5    Castrillon, J.6
  • 19
    • 84874553629 scopus 로고    scopus 로고
    • Circadian-related heteromerization of adrenergic and dopamine D4 receptors modulates melatonin synthesis and release in the pineal gland
    • S. González, D. Moreno-Delgado, E. Moreno, K. Pérez-Capote, R. Franco, and J. Mallol Circadian-related heteromerization of adrenergic and dopamine D4 receptors modulates melatonin synthesis and release in the pineal gland PLoS Biol 10 2012 e1001347
    • (2012) PLoS Biol , vol.10 , pp. 1001347
    • González, S.1    Moreno-Delgado, D.2    Moreno, E.3    Pérez-Capote, K.4    Franco, R.5    Mallol, J.6
  • 21
    • 0029054965 scopus 로고
    • Agonist-receptor efficacy. II. Agonist trafficking of receptor signals
    • T. Kenakin Agonist-receptor efficacy. II. Agonist trafficking of receptor signals Trends Pharmacol Sci 16 1995 232 238
    • (1995) Trends Pharmacol Sci , vol.16 , pp. 232-238
    • Kenakin, T.1
  • 22
    • 84864221004 scopus 로고    scopus 로고
    • A new era of GPCR structural and chemical biology
    • S. Granier, and B. Kobilka A new era of GPCR structural and chemical biology Nat Chem Biol 8 2012 670
    • (2012) Nat Chem Biol , vol.8 , pp. 670
    • Granier, S.1    Kobilka, B.2
  • 24
    • 80054081804 scopus 로고    scopus 로고
    • Ligand-dependent perturbation of the conformational ensemble for the GPCR β2 adrenergic receptor revealed by HDX
    • G.M. West, E.Y.T. Chien, V. Katritch, J. Gatchalian, M.J. Chalmers, and R.C. Stevens Ligand-dependent perturbation of the conformational ensemble for the GPCR β2 adrenergic receptor revealed by HDX Structure 19 2011 1424 1432
    • (2011) Structure , vol.19 , pp. 1424-1432
    • West, G.M.1    Chien, E.Y.T.2    Katritch, V.3    Gatchalian, J.4    Chalmers, M.J.5    Stevens, R.C.6
  • 26
    • 77951877209 scopus 로고    scopus 로고
    • Tracking G-protein-coupled receptor activation using genetically encoded infrared probes
    • S. Ye, E. Zaitseva, G. Caltabiano, G.F.X. Schertler, T.P. Sakmar, and X. Deupi Tracking G-protein-coupled receptor activation using genetically encoded infrared probes Nature 464 2010 1386 1389
    • (2010) Nature , vol.464 , pp. 1386-1389
    • Ye, S.1    Zaitseva, E.2    Caltabiano, G.3    Schertler, G.F.X.4    Sakmar, T.P.5    Deupi, X.6
  • 28
    • 33746382921 scopus 로고    scopus 로고
    • Coupling ligand structure to specific conformational switches in the β2-adrenoceptor
    • X. Yao, C. Parnot, X. Deupi, V.R.P. Ratnala, G. Swaminath, and D. Farrens Coupling ligand structure to specific conformational switches in the β2-adrenoceptor Nat Chem Biol 2 2006 417 422
    • (2006) Nat Chem Biol , vol.2 , pp. 417-422
    • Yao, X.1    Parnot, C.2    Deupi, X.3    Ratnala, V.R.P.4    Swaminath, G.5    Farrens, D.6
  • 29
    • 0345791508 scopus 로고    scopus 로고
    • Sequential binding of agonists to the β2 adrenoceptor. Kinetic evidence for intermediate conformational states
    • G. Swaminath, Y. Xiang, T.W. Lee, J. Steenhuis, C. Parnot, and B.K. Kobilka Sequential binding of agonists to the β2 adrenoceptor. Kinetic evidence for intermediate conformational states J Biol Chem 279 2004 686 691
    • (2004) J Biol Chem , vol.279 , pp. 686-691
    • Swaminath, G.1    Xiang, Y.2    Lee, T.W.3    Steenhuis, J.4    Parnot, C.5    Kobilka, B.K.6
  • 30
    • 0035958925 scopus 로고    scopus 로고
    • Bombesin and substance P analogues differentially regulate G-protein coupling to the bombesin receptor. Direct evidence for biased agonism
    • A.C. MacKinnon, C. Waters, D. Jodrell, C. Haslett, and T. Sethi Bombesin and substance P analogues differentially regulate G-protein coupling to the bombesin receptor. Direct evidence for biased agonism J Biol Chem 276 2001 28083 28091
    • (2001) J Biol Chem , vol.276 , pp. 28083-28091
    • Mackinnon, A.C.1    Waters, C.2    Jodrell, D.3    Haslett, C.4    Sethi, T.5
  • 31
    • 84861429624 scopus 로고    scopus 로고
    • Ligands and signaling proteins govern the conformational landscape explored by a G protein-coupled receptor
    • S. Mary, M. Damian, M. Louet, N. Floquet, J.-A. Fehrentz, and J. Marie Ligands and signaling proteins govern the conformational landscape explored by a G protein-coupled receptor Proc Natl Acad Sci USA 109 2012 8304 8309
    • (2012) Proc Natl Acad Sci USA , vol.109 , pp. 8304-8309
    • Mary, S.1    Damian, M.2    Louet, M.3    Floquet, N.4    Fehrentz, J.-A.5    Marie, J.6
  • 32
    • 84864853215 scopus 로고    scopus 로고
    • Ligand-specific interactions modulate kinetic, energetic, and mechanical properties of the human β2 adrenergic receptor
    • M. Zocher, J.J. Fung, B.K. Kobilka, and D.J. Müller Ligand-specific interactions modulate kinetic, energetic, and mechanical properties of the human β2 adrenergic receptor Structure 20 2012 1391 1402
    • (2012) Structure , vol.20 , pp. 1391-1402
    • Zocher, M.1    Fung, J.J.2    Kobilka, B.K.3    Müller, D.J.4
  • 33
    • 80052027428 scopus 로고    scopus 로고
    • Asymmetry of GPCR oligomers supports their functional relevance
    • P. Maurice, M. Kamal, and R. Jockers Asymmetry of GPCR oligomers supports their functional relevance Trends Pharmacol Sci 32 2011 514 520
    • (2011) Trends Pharmacol Sci , vol.32 , pp. 514-520
    • Maurice, P.1    Kamal, M.2    Jockers, R.3
  • 34
    • 77952415656 scopus 로고    scopus 로고
    • Beyond desensitization: Physiological relevance of arrestin-dependent signaling
    • L.M. Luttrell, and D. Gesty-Palmer Beyond desensitization: physiological relevance of arrestin-dependent signaling Pharmacol Rev 62 2010 305 330
    • (2010) Pharmacol Rev , vol.62 , pp. 305-330
    • Luttrell, L.M.1    Gesty-Palmer, D.2
  • 35
    • 81055145330 scopus 로고    scopus 로고
    • Discovery of β-arrestin-biased dopamine D2 ligands for probing signal transduction pathways essential for antipsychotic efficacy
    • J.A. Allen, J.M. Yost, V. Setola, X. Chen, M.F. Sassano, and M. Chen Discovery of β-arrestin-biased dopamine D2 ligands for probing signal transduction pathways essential for antipsychotic efficacy Proc Natl Acad Sci 108 2011 18488 18493
    • (2011) Proc Natl Acad Sci , vol.108 , pp. 18488-18493
    • Allen, J.A.1    Yost, J.M.2    Setola, V.3    Chen, X.4    Sassano, M.F.5    Chen, M.6
  • 36
    • 79952488185 scopus 로고    scopus 로고
    • Therapeutic potential of β-arrestin- and G protein-biased agonists
    • E.J. Whalen, S. Rajagopal, and R.J. Lefkowitz Therapeutic potential of β-arrestin- and G protein-biased agonists Trends Mol Med 17 2011 126 139
    • (2011) Trends Mol Med , vol.17 , pp. 126-139
    • Whalen, E.J.1    Rajagopal, S.2    Lefkowitz, R.J.3
  • 37
    • 80052768977 scopus 로고    scopus 로고
    • CXCR7/CXCR4 heterodimer constitutively recruits β-arrestin to enhance cell migration
    • F.M. Décaillot, M.A. Kazmi, Y. Lin, S. Ray-Saha, T.P. Sakmar, and P. Sachdev CXCR7/CXCR4 heterodimer constitutively recruits β-arrestin to enhance cell migration J Biol Chem 286 2011 32188 32197
    • (2011) J Biol Chem , vol.286 , pp. 32188-32197
    • Décaillot, F.M.1    Kazmi, M.A.2    Lin, Y.3    Ray-Saha, S.4    Sakmar, T.P.5    Sachdev, P.6
  • 38
    • 74049094108 scopus 로고    scopus 로고
    • Arrestin orchestrates crosstalk between G protein-coupled receptors to modulate the spatiotemporal activation of ERK MAPK
    • D. Cervantes, C. Crosby, and Y. Xiang Arrestin orchestrates crosstalk between G protein-coupled receptors to modulate the spatiotemporal activation of ERK MAPK Circ Res 106 2009 1
    • (2009) Circ Res , vol.106 , pp. 1
    • Cervantes, D.1    Crosby, C.2    Xiang, Y.3
  • 39
    • 84862905449 scopus 로고    scopus 로고
    • Deciphering biased-agonism complexity reveals a new active AT1 receptor entity
    • A. Saulière, M. Bellot, H. Paris, C. Denis, F. Finana, and J.T. Hansen Deciphering biased-agonism complexity reveals a new active AT1 receptor entity Nat Chem Biol 8 2012 622 630
    • (2012) Nat Chem Biol , vol.8 , pp. 622-630
    • Saulière, A.1    Bellot, M.2    Paris, H.3    Denis, C.4    Finana, F.5    Hansen, J.T.6
  • 41
    • 76249134336 scopus 로고    scopus 로고
    • β-arrestin- but not G protein-mediated signaling by the "decoy" receptor CXCR7
    • S. Rajagopal, J. Kim, S. Ahn, S. Craig, C.M. Lam, and N.P. Gerard β-arrestin- but not G protein-mediated signaling by the "decoy" receptor CXCR7 Proc Natl Acad Sci 107 2010 628 632
    • (2010) Proc Natl Acad Sci , vol.107 , pp. 628-632
    • Rajagopal, S.1    Kim, J.2    Ahn, S.3    Craig, S.4    Lam, C.M.5    Gerard, N.P.6
  • 42
    • 67650349084 scopus 로고    scopus 로고
    • CXCR7 heterodimerizes with CXCR4 and regulates CXCL12-mediated G protein signalling
    • A. Levoye, K. Balabanian, F. Baleux, F. Bachelerie, and B. Lagane CXCR7 heterodimerizes with CXCR4 and regulates CXCL12-mediated G protein signalling Blood 113 2009 6085 6093
    • (2009) Blood , vol.113 , pp. 6085-6093
    • Levoye, A.1    Balabanian, K.2    Baleux, F.3    Bachelerie, F.4    Lagane, B.5
  • 43
    • 80052768977 scopus 로고    scopus 로고
    • CXCR7/CXCR4 heterodimer constitutively recruits {beta}-arrestin to enhance cell migration
    • F.M. Decaillot, M.A. Kazmi, Y. Lin, S. Ray-Saha, T.P. Sakmar, and P. Sachdev CXCR7/CXCR4 heterodimer constitutively recruits {beta}-arrestin to enhance cell migration J Biol Chem 286 2011 32188 32197
    • (2011) J Biol Chem , vol.286 , pp. 32188-32197
    • Decaillot, F.M.1    Kazmi, M.A.2    Lin, Y.3    Ray-Saha, S.4    Sakmar, T.P.5    Sachdev, P.6
  • 44
    • 64849108150 scopus 로고    scopus 로고
    • Heterotrimeric G proteins demonstrate differential sensitivity to beta-arrestin dependent desensitization
    • G. Innamorati, F. Giannone, F. Guzzi, G.E. Rovati, M.R. Accomazzo, and B. Chini Heterotrimeric G proteins demonstrate differential sensitivity to beta-arrestin dependent desensitization Cell Signal 21 2009 1135 1142
    • (2009) Cell Signal , vol.21 , pp. 1135-1142
    • Innamorati, G.1    Giannone, F.2    Guzzi, F.3    Rovati, G.E.4    Accomazzo, M.R.5    Chini, B.6
  • 45
    • 84856759440 scopus 로고    scopus 로고
    • Functional selective oxytocin-derived agonists discriminate between individual G protein family subtypes
    • M. Busnelli, A. Saulière, M. Manning, M. Bouvier, C. Galés, and B. Chini Functional selective oxytocin-derived agonists discriminate between individual G protein family subtypes J Biol Chem 287 2012 3617 3629
    • (2012) J Biol Chem , vol.287 , pp. 3617-3629
    • Busnelli, M.1    Saulière, A.2    Manning, M.3    Bouvier, M.4    Galés, C.5    Chini, B.6
  • 46
    • 69249158290 scopus 로고    scopus 로고
    • Allosteric communication between protomers of dopamine class A GPCR dimers modulates activation
    • Y. Han, I.S. Moreira, E. Urizar, H. Weinstein, and J.A. Javitch Allosteric communication between protomers of dopamine class A GPCR dimers modulates activation Nat Chem Biol 5 2009 688 695
    • (2009) Nat Chem Biol , vol.5 , pp. 688-695
    • Han, Y.1    Moreira, I.S.2    Urizar, E.3    Weinstein, H.4    Javitch, J.A.5
  • 47
    • 84860505658 scopus 로고    scopus 로고
    • New insights from structural biology into the druggability of G protein-coupled receptors
    • J.S. Mason, A. Bortolato, M. Congreve, and F.H. Marshall 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
  • 48
    • 67649494337 scopus 로고    scopus 로고
    • Transforming fragments into candidates: Small becomes big in medicinal chemistry
    • G.E. de Kloe, D. Bailey, R. Leurs, and I.J.P. de Esch Transforming fragments into candidates: small becomes big in medicinal chemistry Drug Discov Today 14 2009 630 646
    • (2009) Drug Discov Today , vol.14 , pp. 630-646
    • De Kloe, G.E.1    Bailey, D.2    Leurs, R.3    De Esch, I.J.P.4
  • 49
    • 78650147139 scopus 로고    scopus 로고
    • Allostery at G protein-coupled receptor homo- and heteromers: Uncharted pharmacological landscapes
    • N.J. Smith, and G. Milligan Allostery at G protein-coupled receptor homo- and heteromers: uncharted pharmacological landscapes Pharmacol Rev 62 2010 701 725
    • (2010) Pharmacol Rev , vol.62 , pp. 701-725
    • Smith, N.J.1    Milligan, G.2
  • 50
    • 67650373914 scopus 로고    scopus 로고
    • Screening technologies for G protein-coupled receptors: From HTS to uHTS
    • M. De los Frailes, and E. Diez Screening technologies for G protein-coupled receptors: from HTS to uHTS Methods Mol Biol 552 2009 15 37
    • (2009) Methods Mol Biol , vol.552 , pp. 15-37
    • De Los Frailes, M.1    Diez, E.2
  • 51
    • 0028950255 scopus 로고
    • The two-state model of receptor activation
    • P. Leff The two-state model of receptor activation Trends Pharmacol Sci 16 1995 89 97
    • (1995) Trends Pharmacol Sci , vol.16 , pp. 89-97
    • Leff, P.1
  • 53
    • 3042798261 scopus 로고    scopus 로고
    • Molecular mechanisms of ligand binding, signaling, and regulation within the superfamily of G-protein-coupled receptors: Molecular modeling and mutagenesis approaches to receptor structure and function
    • K. Kristiansen Molecular mechanisms of ligand binding, signaling, and regulation within the superfamily of G-protein-coupled receptors: molecular modeling and mutagenesis approaches to receptor structure and function Pharmacol Ther 103 2004 21 80
    • (2004) Pharmacol Ther , vol.103 , pp. 21-80
    • Kristiansen, K.1
  • 54
    • 38749131545 scopus 로고    scopus 로고
    • New G-protein-coupled receptor crystal structures: Insights and limitations
    • B. Kobilka, and G.F.X. Schertler New G-protein-coupled receptor crystal structures: insights and limitations Trends Pharmacol Sci 29 2008 79 83
    • (2008) Trends Pharmacol Sci , vol.29 , pp. 79-83
    • Kobilka, B.1    Schertler, G.F.X.2
  • 55
    • 77956398267 scopus 로고    scopus 로고
    • Orthosteric- and allosteric-induced ligand-directed trafficking at GPCRs
    • G.J. Digby, P.J. Conn, and C.W. Lindsley Orthosteric- and allosteric-induced ligand-directed trafficking at GPCRs Curr Opin Drug Discov Devel 13 2010 587 594
    • (2010) Curr Opin Drug Discov Devel , vol.13 , pp. 587-594
    • Digby, G.J.1    Conn, P.J.2    Lindsley, C.W.3
  • 57
    • 33747181100 scopus 로고    scopus 로고
    • Allosteric agonists of 7TM receptors: Expanding the pharmacological toolbox
    • C.J. Langmead, and A. Christopoulos Allosteric agonists of 7TM receptors: expanding the pharmacological toolbox Trends Pharmacol Sci 27 2006 475 481
    • (2006) Trends Pharmacol Sci , vol.27 , pp. 475-481
    • Langmead, C.J.1    Christopoulos, A.2
  • 58
    • 70349109589 scopus 로고    scopus 로고
    • GPCR homomers and heteromers: A better choice as targets for drug development than GPCR monomers?
    • V. Casadó, A. Cortés, J. Mallol, K. Pérez-Capote, S. Ferré, and C. Lluis GPCR homomers and heteromers: a better choice as targets for drug development than GPCR monomers? Pharmacol Ther 124 2009 248 257
    • (2009) Pharmacol Ther , vol.124 , pp. 248-257
    • Casadó, V.1    Cortés, A.2    Mallol, J.3    Pérez-Capote, K.4    Ferré, S.5    Lluis, C.6
  • 59
    • 36249020990 scopus 로고    scopus 로고
    • Old and new ways to calculate the affinity of agonists and antagonists interacting with G-protein-coupled monomeric and dimeric receptors: The receptor-dimer cooperativity index
    • V. Casadó, A. Cortés, F. Ciruela, J. Mallol, S. Ferré, and C. Lluis Old and new ways to calculate the affinity of agonists and antagonists interacting with G-protein-coupled monomeric and dimeric receptors: the receptor-dimer cooperativity index Pharmacol Ther 116 2007 343 354
    • (2007) Pharmacol Ther , vol.116 , pp. 343-354
    • Casadó, V.1    Cortés, A.2    Ciruela, F.3    Mallol, J.4    Ferré, S.5    Lluis, C.6
  • 60
    • 33745127060 scopus 로고    scopus 로고
    • The two-state dimer receptor model: A general model for receptor dimers
    • R. Franco, V. Casadó, J. Mallol, C. Ferrada, S. Ferré, and K. Fuxe The two-state dimer receptor model: a general model for receptor dimers Mol Pharmacol 69 2006 1905 1912
    • (2006) Mol Pharmacol , vol.69 , pp. 1905-1912
    • Franco, R.1    Casadó, V.2    Mallol, J.3    Ferrada, C.4    Ferré, S.5    Fuxe, K.6
  • 62
    • 79956317677 scopus 로고    scopus 로고
    • G protein-coupled receptor heteromerization: A role in allosteric modulation of ligand binding
    • I. Gomes, A.P. Ijzerman, K. Ye, E.L. Maillet, and L.A. Devi G protein-coupled receptor heteromerization: a role in allosteric modulation of ligand binding Mol Pharmacol 79 2011 1044 1052
    • (2011) Mol Pharmacol , vol.79 , pp. 1044-1052
    • Gomes, I.1    Ijzerman, A.P.2    Ye, K.3    Maillet, E.L.4    Devi, L.A.5
  • 64
    • 84861523769 scopus 로고    scopus 로고
    • Metabotropic glutamate receptor 4 (mGlu4)-positive allosteric modulators for the treatment of Parkinson's disease: Historical perspective and review of the patent literature
    • C.W. Lindsley, and C.R. Hopkins Metabotropic glutamate receptor 4 (mGlu4)-positive allosteric modulators for the treatment of Parkinson's disease: historical perspective and review of the patent literature Expert Opin Ther Pat 22 2012 461 481
    • (2012) Expert Opin Ther Pat , vol.22 , pp. 461-481
    • Lindsley, C.W.1    Hopkins, C.R.2
  • 65
    • 84864462348 scopus 로고    scopus 로고
    • Allosteric modulators of rhodopsin-like G protein-coupled receptors: Opportunities in drug development
    • C.E. Müller, A.C. Schiedel, and Y. Baqi Allosteric modulators of rhodopsin-like G protein-coupled receptors: opportunities in drug development Pharmacol Ther 135 2012 292 315
    • (2012) Pharmacol Ther , vol.135 , pp. 292-315
    • Müller, C.E.1    Schiedel, A.C.2    Baqi, Y.3
  • 68
    • 33644551294 scopus 로고    scopus 로고
    • Presynaptic control of striatal glutamatergic neurotransmission by adenosine A1-A2A receptor heteromers
    • F. Ciruela, V. Casadó, R.J. Rodrigues, R. Luján, J. Burgueño, and M. Canals Presynaptic control of striatal glutamatergic neurotransmission by adenosine A1-A2A receptor heteromers J Neurosci 26 2006 2080 2087
    • (2006) J Neurosci , vol.26 , pp. 2080-2087
    • Ciruela, F.1    Casadó, V.2    Rodrigues, R.J.3    Luján, R.4    Burgueño, J.5    Canals, M.6
  • 69
    • 33846328669 scopus 로고    scopus 로고
    • D1-D2 dopamine receptor heterooligomers with unique pharmacology are coupled to rapid activation of Gq/11 in the striatum
    • A.J. Rashid, C.H. So, M.M. Kong, T. Furtak, M. El-Ghundi, and R. Cheng D1-D2 dopamine receptor heterooligomers with unique pharmacology are coupled to rapid activation of Gq/11 in the striatum Proc Natl Acad Sci USA 104 2007 654 659
    • (2007) Proc Natl Acad Sci USA , vol.104 , pp. 654-659
    • Rashid, A.J.1    So, C.H.2    Kong, M.M.3    Furtak, T.4    El-Ghundi, M.5    Cheng, R.6
  • 70
    • 0035811447 scopus 로고    scopus 로고
    • From models to molecules: Opioid receptor dimers, bivalent ligands, and selective opioid receptor probes
    • P.S. Portoghese From models to molecules: opioid receptor dimers, bivalent ligands, and selective opioid receptor probes J Med Chem 44 2001 2259 2269
    • (2001) J Med Chem , vol.44 , pp. 2259-2269
    • Portoghese, P.S.1
  • 71
    • 84855879360 scopus 로고    scopus 로고
    • The best of both worlds? Bitopic orthosteric/allosteric ligands of g protein-coupled receptors
    • C. Valant, L.J. Robert, P.M. Sexton, and A. Christopoulos The best of both worlds? Bitopic orthosteric/allosteric ligands of g protein-coupled receptors Annu Rev Pharmacol Toxicol 52 2012 153 178
    • (2012) Annu Rev Pharmacol Toxicol , vol.52 , pp. 153-178
    • Valant, C.1    Robert, L.J.2    Sexton, P.M.3    Christopoulos, A.4
  • 72
    • 70349192980 scopus 로고    scopus 로고
    • Adenosine A2A receptor-antagonist/dopamine D2 receptor-agonist bivalent ligands as pharmacological tools to detect A2A-D2 receptor heteromers
    • A. Soriano, R. Ventura, A. Molero, R. Hoen, V. Casadó, and A. Cortés Adenosine A2A receptor-antagonist/dopamine D2 receptor-agonist bivalent ligands as pharmacological tools to detect A2A-D2 receptor heteromers J Med Chem 52 2009 5590 5602
    • (2009) J Med Chem , vol.52 , pp. 5590-5602
    • Soriano, A.1    Ventura, R.2    Molero, A.3    Hoen, R.4    Casadó, V.5    Cortés, A.6
  • 73
    • 79960172993 scopus 로고    scopus 로고
    • Bivalent dopamine D2 receptor ligands: Synthesis and binding properties
    • J. Kühhorn, H. Hübner, and P. Gmeiner Bivalent dopamine D2 receptor ligands: synthesis and binding properties J Med Chem 54 2011 4896 4903
    • (2011) J Med Chem , vol.54 , pp. 4896-4903
    • Kühhorn, J.1    Hübner, H.2    Gmeiner, P.3
  • 74
    • 34548487956 scopus 로고    scopus 로고
    • Synthesis of specific bivalent probes that functionally interact with 5-HT(4) receptor dimers
    • O. Russo, M. Berthouze, M. Giner, J.L. Soulier, L. Rivail, and S. Sicsic Synthesis of specific bivalent probes that functionally interact with 5-HT(4) receptor dimers J Med Chem 50 2007 4482 4492
    • (2007) J Med Chem , vol.50 , pp. 4482-4492
    • Russo, O.1    Berthouze, M.2    Giner, M.3    Soulier, J.L.4    Rivail, L.5    Sicsic, S.6
  • 75
    • 10544224535 scopus 로고    scopus 로고
    • Serotonin dimers: Application of the bivalent ligand approach to the design of new potent and selective 5-HT(1B/1D) agonists
    • S. Halazy, M. Perez, C. Fourrier, I. Pallard, P.J. Pauwels, and C. Palmier Serotonin dimers: application of the bivalent ligand approach to the design of new potent and selective 5-HT(1B/1D) agonists J Med Chem 39 1996 4920 4927
    • (1996) J Med Chem , vol.39 , pp. 4920-4927
    • Halazy, S.1    Perez, M.2    Fourrier, C.3    Pallard, I.4    Pauwels, P.J.5    Palmier, C.6
  • 76
    • 34547181796 scopus 로고    scopus 로고
    • Synthesis and evaluation of bivalent NDP-alpha-MSH(7) peptide ligands for binding to the human melanocortin receptor 4 (hMC4R)
    • H.L. Handl, R. Sankaranarayanan, J.S. Josan, J. Vagner, E.A. Mash, and R.J. Gillies Synthesis and evaluation of bivalent NDP-alpha-MSH(7) peptide ligands for binding to the human melanocortin receptor 4 (hMC4R) Bioconjug Chem 18 2007 1101 1109
    • (2007) Bioconjug Chem , vol.18 , pp. 1101-1109
    • Handl, H.L.1    Sankaranarayanan, R.2    Josan, J.S.3    Vagner, J.4    Mash, E.A.5    Gillies, R.J.6
  • 77
    • 84863362554 scopus 로고    scopus 로고
    • Design and synthesis of a bivalent ligand to explore the putative heterodimerization of the mu opioid receptor and the chemokine receptor CCR5
    • Y. Yuan, C.K. Arnatt, G. Li, K.M. Haney, D. Ding, and J.C. Jacob Design and synthesis of a bivalent ligand to explore the putative heterodimerization of the mu opioid receptor and the chemokine receptor CCR5 Org Biomol Chem 10 2012 2633 2646
    • (2012) Org Biomol Chem , vol.10 , pp. 2633-2646
    • Yuan, Y.1    Arnatt, C.K.2    Li, G.3    Haney, K.M.4    Ding, D.5    Jacob, J.C.6
  • 80
    • 27144548417 scopus 로고    scopus 로고
    • Dimerization of chemokine receptors and its functional consequences
    • J.Y. Springael, E. Urizar, and M. Parmentier Dimerization of chemokine receptors and its functional consequences Cytokine Growth Factor Rev 16 2005 611 623
    • (2005) Cytokine Growth Factor Rev , vol.16 , pp. 611-623
    • Springael, J.Y.1    Urizar, E.2    Parmentier, M.3
  • 81
    • 78449262856 scopus 로고    scopus 로고
    • Bivalent ligands of CXCR4 with rigid linkers for elucidation of the dimerization state in cells
    • T. Tanaka, W. Nomura, T. Narumi, A. Masuda, and H. Tamamura Bivalent ligands of CXCR4 with rigid linkers for elucidation of the dimerization state in cells J Am Chem Soc 132 2010 15899 15901
    • (2010) J Am Chem Soc , vol.132 , pp. 15899-15901
    • Tanaka, T.1    Nomura, W.2    Narumi, T.3    Masuda, A.4    Tamamura, H.5
  • 83
    • 75849140535 scopus 로고    scopus 로고
    • Calcium signaling cascade links dopamine D1-D2 receptor heteromer to striatal BDNF production and neuronal growth
    • A. Hasbi, T. Fan, M. Alijaniaram, T. Nguyen, M.L. Perreault, and B.F. O'Dowd Calcium signaling cascade links dopamine D1-D2 receptor heteromer to striatal BDNF production and neuronal growth Proc Natl Acad Sci USA 106 2009 21377 21382
    • (2009) Proc Natl Acad Sci USA , vol.106 , pp. 21377-21382
    • Hasbi, A.1    Fan, T.2    Alijaniaram, M.3    Nguyen, T.4    Perreault, M.L.5    O'Dowd, B.F.6
  • 86
    • 51849124172 scopus 로고    scopus 로고
    • A homogeneous G protein-coupled receptor ligand binding assay based on time-resolved fluorescence resonance energy transfer
    • L.A. Hu, T. Zhou, B.D. Hamman, and Q. Liu A homogeneous G protein-coupled receptor ligand binding assay based on time-resolved fluorescence resonance energy transfer Assay Drug Dev Technol 6 2008 543 550
    • (2008) Assay Drug Dev Technol , vol.6 , pp. 543-550
    • Hu, L.A.1    Zhou, T.2    Hamman, B.D.3    Liu, Q.4
  • 87
    • 84874181001 scopus 로고    scopus 로고
    • Enhanced BRET technology for the monitoring of agonist-induced and agonist-independent interactions between GPCRs and β-arrestins
    • M. Kocan, M.B. Dalrymple, R.M. Seeber, B.J. Feldman, and K.D. Pfleger Enhanced BRET technology for the monitoring of agonist-induced and agonist-independent interactions between GPCRs and β-arrestins Front Endocrinol 1 2010 12
    • (2010) Front Endocrinol , vol.1 , pp. 12
    • Kocan, M.1    Dalrymple, M.B.2    Seeber, R.M.3    Feldman, B.J.4    Pfleger, K.D.5
  • 88
    • 79951713324 scopus 로고    scopus 로고
    • Application of G protein-coupled receptor-heteromer identification technology to monitor β-arrestin recruitment to G protein-coupled receptor heteromers
    • H.B. See, R.M. Seeber, M. Kocan, K.A. Eidne, and K.D. Pfleger Application of G protein-coupled receptor-heteromer identification technology to monitor β-arrestin recruitment to G protein-coupled receptor heteromers Assay Drug Dev Technol 9 2011 21 30
    • (2011) Assay Drug Dev Technol , vol.9 , pp. 21-30
    • See, H.B.1    Seeber, R.M.2    Kocan, M.3    Eidne, K.A.4    Pfleger, K.D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.