-
1
-
-
79961007572
-
Trends in the exploitation of novel drug targets
-
Rask-Andersen, M., Almén, M. S., and Schiöth, H. B. (2011) Trends in the exploitation of novel drug targets Nat. Rev. Drug Discovery 10, 579-590
-
(2011)
Nat. Rev. Drug Discovery
, vol.10
, pp. 579-590
-
-
Rask-Andersen, M.1
Almén, M.S.2
Schiöth, H.B.3
-
2
-
-
0036490942
-
Allosteric binding sites on cell-surface receptors: Novel targets for drug discovery
-
Christopoulos, A. (2002) Allosteric binding sites on cell-surface receptors: novel targets for drug discovery Nat. Rev. Drug Discovery 1, 198-210
-
(2002)
Nat. Rev. Drug Discovery
, vol.1
, pp. 198-210
-
-
Christopoulos, A.1
-
3
-
-
58149193205
-
Allosteric modulators of GPCRs: A novel approach for the treatment of CNS disorders
-
Conn, P., Christopoulos, A., and Lindsley, C. (2009) Allosteric modulators of GPCRs: a novel approach for the treatment of CNS disorders Nat. Rev. Drug Discovery 8, 41-54
-
(2009)
Nat. Rev. Drug Discovery
, vol.8
, pp. 41-54
-
-
Conn, P.1
Christopoulos, A.2
Lindsley, C.3
-
4
-
-
77952354490
-
Seven transmembrane receptors as shapeshifting proteins: The impact of allosteric modulation and functional selectivity on new drug discovery
-
Kenakin, T. and Miller, L. J. (2010) Seven transmembrane receptors as shapeshifting proteins: the impact of allosteric modulation and functional selectivity on new drug discovery Pharmacol. Rev. 62, 265-304
-
(2010)
Pharmacol. Rev.
, vol.62
, pp. 265-304
-
-
Kenakin, T.1
Miller, L.J.2
-
5
-
-
79960502280
-
Ligand functional selectivity and quantitative pharmacology at G protein-coupled receptors
-
Stallaert, W., Christopoulos, A., and Bouvier, M. (2011) Ligand functional selectivity and quantitative pharmacology at G protein-coupled receptors Expert Opin. Drug Discovery 6, 811-825
-
(2011)
Expert Opin. Drug Discovery
, vol.6
, pp. 811-825
-
-
Stallaert, W.1
Christopoulos, A.2
Bouvier, M.3
-
6
-
-
79952488185
-
Therapeutic potential of β-arrestin- and G protein-biased agonists
-
Whalen, E. J., Rajagopal, S., and Lefkowitz, R. J. (2011) Therapeutic potential of β-arrestin- and G protein-biased agonists Trends Mol. Med. 17, 126-139
-
(2011)
Trends Mol. Med.
, vol.17
, pp. 126-139
-
-
Whalen, E.J.1
Rajagopal, S.2
Lefkowitz, R.J.3
-
7
-
-
80051658642
-
Crystal structure of the β2 adrenergic receptor-Gs protein complex
-
Rasmussen, S. G. F., Devree, B. T., Zou, Y., Kruse, A. C., Chung, K. Y., Kobilka, T. S., Thian, F. S., Chae, P. S., Pardon, E., Calinski, D., Mathiesen, J. M., Shah, S. T. A., Lyons, J. A., Caffrey, M., Gellman, S. H., Steyaert, J., Skiniotis, G., Weis, W. I., Sunahara, R. K., and Kobilka, B. K. (2011) Crystal structure of the β2 adrenergic receptor-Gs protein complex Nature 477, 549-555
-
(2011)
Nature
, vol.477
, pp. 549-555
-
-
Rasmussen, S.G.F.1
Devree, B.T.2
Zou, Y.3
Kruse, A.C.4
Chung, K.Y.5
Kobilka, T.S.6
Thian, F.S.7
Chae, P.S.8
Pardon, E.9
Calinski, D.10
Mathiesen, J.M.11
Shah, S.T.A.12
Lyons, J.A.13
Caffrey, M.14
Gellman, S.H.15
Steyaert, J.16
Skiniotis, G.17
Weis, W.I.18
Sunahara, R.K.19
Kobilka, B.K.20
more..
-
8
-
-
0347949548
-
Insights into G protein structure, function, and regulation
-
Cabrera-Vera, T. M., Vanhauwe, J., Thomas, T. O., Medkova, M., Preininger, A., Mazzoni, M. R., and Hamm, H. E. (2003) Insights into G protein structure, function, and regulation Endocr. Rev. 24, 765-781
-
(2003)
Endocr. Rev.
, vol.24
, pp. 765-781
-
-
Cabrera-Vera, T.M.1
Vanhauwe, J.2
Thomas, T.O.3
Medkova, M.4
Preininger, A.5
Mazzoni, M.R.6
Hamm, H.E.7
-
9
-
-
2942618584
-
Beta-arrestins: Traffic cops of cell signaling
-
Lefkowitz, R. J. and Whalen, E. J. (2004) beta-arrestins: traffic cops of cell signaling Curr. Opin. Cell Biol. 16, 162-168
-
(2004)
Curr. Opin. Cell Biol.
, vol.16
, pp. 162-168
-
-
Lefkowitz, R.J.1
Whalen, E.J.2
-
10
-
-
33947401068
-
β-Arrestins and Cell Signaling
-
DeWire, S. M., Ahn, S., Lefkowitz, R. J., and Shenoy, S. K. (2007) β-Arrestins and Cell Signaling Annu. Rev. Physiol. 69, 483-510
-
(2007)
Annu. Rev. Physiol.
, vol.69
, pp. 483-510
-
-
Dewire, S.M.1
Ahn, S.2
Lefkowitz, R.J.3
Shenoy, S.K.4
-
11
-
-
70449552889
-
Endosomes: A legitimate platform for the signaling train
-
Murphy, J. E., Padilla, B. E., Hasdemir, B., Cottrell, G. S., and Bunnett, N. W. (2009) Endosomes: a legitimate platform for the signaling train Proc. Natl. Acad. Sci. U.S.A. 106, 17615-17622
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 17615-17622
-
-
Murphy, J.E.1
Padilla, B.E.2
Hasdemir, B.3
Cottrell, G.S.4
Bunnett, N.W.5
-
12
-
-
33847122495
-
Allosteric modulation of G protein-coupled receptors
-
May, L., Leach, K., Sexton, P., and Christopoulos, A. (2007) Allosteric modulation of G protein-coupled receptors Annu. Rev. Pharmacol. Toxicol. 47, 1-51
-
(2007)
Annu. Rev. Pharmacol. Toxicol.
, vol.47
, pp. 1-51
-
-
May, L.1
Leach, K.2
Sexton, P.3
Christopoulos, A.4
-
13
-
-
27644510382
-
Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity
-
Dorr, P., Westby, M., Dobbs, S., Griffin, P., Irvine, B., Macartney, M., Mori, J., Rickett, G., Smith-Burchnell, C., Napier, C., Webster, R., Armour, D., Price, D., Stammen, B., Wood, A., and Perros, M. (2005) Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity Antimicrob. Agents Chemother. 49, 4721-4732
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 4721-4732
-
-
Dorr, P.1
Westby, M.2
Dobbs, S.3
Griffin, P.4
Irvine, B.5
MacArtney, M.6
Mori, J.7
Rickett, G.8
Smith-Burchnell, C.9
Napier, C.10
Webster, R.11
Armour, D.12
Price, D.13
Stammen, B.14
Wood, A.15
Perros, M.16
-
14
-
-
20544460709
-
Cinacalcet HCl, an Oral Calcimimetic Agent for the Treatment of Secondary Hyperparathyroidism in Hemodialysis and Peritoneal Dialysis: A Randomized, Double-Blind, Multicenter Study
-
Lindberg, J. S. (2005) Cinacalcet HCl, an Oral Calcimimetic Agent for the Treatment of Secondary Hyperparathyroidism in Hemodialysis and Peritoneal Dialysis: A Randomized, Double-Blind, Multicenter Study J. Am. Soc. Nephrol. 16, 800-807
-
(2005)
J. Am. Soc. Nephrol.
, vol.16
, pp. 800-807
-
-
Lindberg, J.S.1
-
15
-
-
78651189765
-
On the nature of allosteric transitions: A plausible model
-
Monod, J., Wyman, J., and Changeux, J.-P. (1965) On the nature of allosteric transitions: a plausible model J. Mol. Biol. 88-118
-
(1965)
J. Mol. Biol.
, pp. 88-118
-
-
Monod, J.1
Wyman, J.2
Changeux, J.-P.3
-
16
-
-
84855290525
-
A Monod-Wyman-Changeux Mechanism Can Explain G Protein-coupled Receptor (GPCR) Allosteric Modulation
-
Canals, M., Lane, J. R., Wen, A., Scammells, P. J., Sexton, P. M., and Christopoulos, A. (2012) A Monod-Wyman-Changeux Mechanism Can Explain G Protein-coupled Receptor (GPCR) Allosteric Modulation J. Biol. Chem. 287, 650-659
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 650-659
-
-
Canals, M.1
Lane, J.R.2
Wen, A.3
Scammells, P.J.4
Sexton, P.M.5
Christopoulos, A.6
-
17
-
-
82355169577
-
Allostery in GPCRs: "mWC" revisited
-
Canals, M., Sexton, P. M., and Christopoulos, A. (2011) Allostery in GPCRs: "MWC" revisited Trends Biochem. Sci. 36, 663-672
-
(2011)
Trends Biochem. Sci.
, vol.36
, pp. 663-672
-
-
Canals, M.1
Sexton, P.M.2
Christopoulos, A.3
-
18
-
-
0018099810
-
GABAergic modulation of benzodiazepine binding site sensitivity
-
Tallman, J. F., Thomas, J. W., and Gallager, D. W. (1978) GABAergic modulation of benzodiazepine binding site sensitivity Nature 274, 383-385
-
(1978)
Nature
, vol.274
, pp. 383-385
-
-
Tallman, J.F.1
Thomas, J.W.2
Gallager, D.W.3
-
19
-
-
0030693304
-
The benzodiazepine binding site of GABAA receptors
-
Sigel, E. and Buhr, A. (1997) The benzodiazepine binding site of GABAA receptors Trends Pharmacol. Sci. 18, 425-429
-
(1997)
Trends Pharmacol. Sci.
, vol.18
, pp. 425-429
-
-
Sigel, E.1
Buhr, A.2
-
20
-
-
42349109493
-
GABA(A) receptor trafficking and its role in the dynamic modulation of neuronal inhibition
-
Jacob, T. C., Moss, S. J., and Jurd, R. (2008) GABA(A) receptor trafficking and its role in the dynamic modulation of neuronal inhibition Nat. Rev. Neurosci. 9, 331-343
-
(2008)
Nat. Rev. Neurosci.
, vol.9
, pp. 331-343
-
-
Jacob, T.C.1
Moss, S.J.2
Jurd, R.3
-
21
-
-
84862068720
-
Regulation of neuronal GABA(B) receptor functions by subunit composition
-
Gassmann, M. and Bettler, B. (2012) Regulation of neuronal GABA(B) receptor functions by subunit composition Nat. Rev. Neurosci. 13, 380-394
-
(2012)
Nat. Rev. Neurosci.
, vol.13
, pp. 380-394
-
-
Gassmann, M.1
Bettler, B.2
-
22
-
-
77949392957
-
Regulation of GABA(A) receptor subunit expression by pharmacological agents
-
Uusi-Oukari, M. and Korpi, E. R. (2010) Regulation of GABA(A) receptor subunit expression by pharmacological agents Pharmacol. Rev. 62, 97-135
-
(2010)
Pharmacol. Rev.
, vol.62
, pp. 97-135
-
-
Uusi-Oukari, M.1
Korpi, E.R.2
-
23
-
-
84868560218
-
Benzodiazepine treatment induces subtype-specific changes in GABAA receptor trafficking and decreases synaptic inhibition
-
Jacob, T. C., Michels, G., Silayeva, L., Haydon, J., Succol, F., and Moss, S. J. (2012) Benzodiazepine treatment induces subtype-specific changes in GABAA receptor trafficking and decreases synaptic inhibition Proc. Natl. Acad. Sci. U.S.A. 109, 18595-18600
-
(2012)
Proc. Natl. Acad. Sci. U.S.A.
, vol.109
, pp. 18595-18600
-
-
Jacob, T.C.1
Michels, G.2
Silayeva, L.3
Haydon, J.4
Succol, F.5
Moss, S.J.6
-
24
-
-
76749144987
-
Molecular Mechanisms of Action and in Vivo Validation of an M4Muscarinic Acetylcholine Receptor Allosteric Modulator with Potential Antipsychotic Properties
-
Leach, K., Loiacono, R., Felder, C., McKinzie, D., Mogg, A., Shaw, D., Sexton, P., and Christopoulos, A. (2009) Molecular Mechanisms of Action and In Vivo Validation of an M4Muscarinic Acetylcholine Receptor Allosteric Modulator with Potential Antipsychotic Properties Neuropsychopharmacology 35, 855-869
-
(2009)
Neuropsychopharmacology
, vol.35
, pp. 855-869
-
-
Leach, K.1
Loiacono, R.2
Felder, C.3
McKinzie, D.4
Mogg, A.5
Shaw, D.6
Sexton, P.7
Christopoulos, A.8
-
25
-
-
11844253226
-
Regulation of M2 muscarinic acetylcholine receptor expression and signaling by prolonged exposure to allosteric modulators
-
May, L. T., Lin, Y., Sexton, P. M., and Christopoulos, A. (2005) Regulation of M2 muscarinic acetylcholine receptor expression and signaling by prolonged exposure to allosteric modulators J. Pharmacol. Exp. Ther. 312, 382-390
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.312
, pp. 382-390
-
-
May, L.T.1
Lin, Y.2
Sexton, P.M.3
Christopoulos, A.4
-
26
-
-
34548476934
-
Critical role for the second extracellular loop in the binding of both orthosteric and allosteric G protein-coupled receptor ligands
-
Avlani, V. A., Gregory, K. J., Morton, C. J., Parker, M. W., Sexton, P. M., and Christopoulos, A. (2007) Critical role for the second extracellular loop in the binding of both orthosteric and allosteric G protein-coupled receptor ligands J. Biol. Chem. 282, 25677-25686
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 25677-25686
-
-
Avlani, V.A.1
Gregory, K.J.2
Morton, C.J.3
Parker, M.W.4
Sexton, P.M.5
Christopoulos, A.6
-
27
-
-
73149088166
-
Differential regulation of muscarinic M1 receptors by orthosteric and allosteric ligands
-
Davis, C., Bradley, S., Schiffer, H., Friberg, M., Koch, K., Tolf, B.-R., Bonhaus, D., and Lameh, J. (2009) Differential regulation of muscarinic M1 receptors by orthosteric and allosteric ligands BMC Pharmacol. 9, 9-14
-
(2009)
BMC Pharmacol.
, vol.9
, pp. 9-14
-
-
Davis, C.1
Bradley, S.2
Schiffer, H.3
Friberg, M.4
Koch, K.5
Tolf, B.-R.6
Bonhaus, D.7
Lameh, J.8
-
28
-
-
77955887321
-
Differential effects of allosteric M(1) muscarinic acetylcholine receptor agonists on receptor activation, arrestin 3 recruitment, and receptor downregulation
-
Davis, A. A., Heilman, C. J., Brady, A. E., Miller, N. R., Fuerstenau-Sharp, M., Hanson, B. J., Lindsley, C. W., Conn, P. J., Lah, J. J., and Levey, A. I. (2010) Differential effects of allosteric M(1) muscarinic acetylcholine receptor agonists on receptor activation, arrestin 3 recruitment, and receptor downregulation ACS. Chem. Neurosci. 1, 542-551
-
(2010)
ACS. Chem. Neurosci.
, vol.1
, pp. 542-551
-
-
Davis, A.A.1
Heilman, C.J.2
Brady, A.E.3
Miller, N.R.4
Fuerstenau-Sharp, M.5
Hanson, B.J.6
Lindsley, C.W.7
Conn, P.J.8
Lah, J.J.9
Levey, A.I.10
-
29
-
-
73349107462
-
Contrasting effects of allosteric and orthosteric agonists on m1 muscarinic acetylcholine receptor internalization and down-regulation
-
Thomas, R. L., Langmead, C. J., Wood, M. D., and Challiss, R. A. J. (2009) Contrasting effects of allosteric and orthosteric agonists on m1 muscarinic acetylcholine receptor internalization and down-regulation J. Pharmacol. Exp. Ther. 331, 1086-1095
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.331
, pp. 1086-1095
-
-
Thomas, R.L.1
Langmead, C.J.2
Wood, M.D.3
Challiss, R.A.J.4
-
30
-
-
70349441133
-
Selective activation of the M1 muscarinic acetylcholine receptor achieved by allosteric potentiation
-
Ma, L., Seager, M. A., Seager, M., Wittmann, M., Jacobson, M., Bickel, D., Burno, M., Jones, K., Graufelds, V. K., Xu, G., Pearson, M., McCampbell, A., Gaspar, R., Shughrue, P., Danziger, A., Regan, C., Flick, R., Pascarella, D., Garson, S., Doran, S., Kreatsoulas, C., Veng, L., Lindsley, C. W., Shipe, W., Kuduk, S., Sur, C., Kinney, G., Seabrook, G. R., and Ray, W. J. (2009) Selective activation of the M1 muscarinic acetylcholine receptor achieved by allosteric potentiation Proc. Natl. Acad. Sci. U.S.A. 106, 15950-15955
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 15950-15955
-
-
Ma, L.1
Seager, M.A.2
Seager, M.3
Wittmann, M.4
Jacobson, M.5
Bickel, D.6
Burno, M.7
Jones, K.8
Graufelds, V.K.9
Xu, G.10
Pearson, M.11
McCampbell, A.12
Gaspar, R.13
Shughrue, P.14
Danziger, A.15
Regan, C.16
Flick, R.17
Pascarella, D.18
Garson, S.19
Doran, S.20
Kreatsoulas, C.21
Veng, L.22
Lindsley, C.W.23
Shipe, W.24
Kuduk, S.25
Sur, C.26
Kinney, G.27
Seabrook, G.R.28
Ray, W.J.29
more..
-
32
-
-
77956256197
-
Comparative effects of the endogenous agonist glucagon-like peptide-1 (GLP-1)-(7-36) amide and the small-molecule ago-allosteric agent "compound 2" at the GLP-1 receptor
-
Coopman, K., Huang, Y., Johnston, N., Bradley, S. J., Wilkinson, G. F., and Willars, G. B. (2010) Comparative effects of the endogenous agonist glucagon-like peptide-1 (GLP-1)-(7-36) amide and the small-molecule ago-allosteric agent "compound 2" at the GLP-1 receptor J. Pharmacol. Exp. Ther. 334, 795-808
-
(2010)
J. Pharmacol. Exp. Ther.
, vol.334
, pp. 795-808
-
-
Coopman, K.1
Huang, Y.2
Johnston, N.3
Bradley, S.J.4
Wilkinson, G.F.5
Willars, G.B.6
-
34
-
-
33845871976
-
MGluR7 undergoes rapid internalization in response to activation by the allosteric agonist AMN082
-
Pelkey, K. A., Yuan, X., Lavezzari, G., Roche, K. W., and McBain, C. J. (2007) mGluR7 undergoes rapid internalization in response to activation by the allosteric agonist AMN082 Neuropharmacology 52, 108-117
-
(2007)
Neuropharmacology
, vol.52
, pp. 108-117
-
-
Pelkey, K.A.1
Yuan, X.2
Lavezzari, G.3
Roche, K.W.4
McBain, C.J.5
-
35
-
-
84856091327
-
Differential effects of the mGluR5 positive allosteric modulator CDPPB in the cortex and striatum following repeated administration
-
Parmentier-Batteur, S., Obrien, J. A., Doran, S., Nguyen, S. J., Flick, R. B., Uslaner, J. M., Chen, H., Finger, E. N., Williams, T. M., Jacobson, M. A., and Hutson, P. H. (2012) Differential effects of the mGluR5 positive allosteric modulator CDPPB in the cortex and striatum following repeated administration Neuropharmacology 62, 1453-1460
-
(2012)
Neuropharmacology
, vol.62
, pp. 1453-1460
-
-
Parmentier-Batteur, S.1
Obrien, J.A.2
Doran, S.3
Nguyen, S.J.4
Flick, R.B.5
Uslaner, J.M.6
Chen, H.7
Finger, E.N.8
Williams, T.M.9
Jacobson, M.A.10
Hutson, P.H.11
-
36
-
-
34248139121
-
Rescue of calcium-sensing receptor mutants by allosteric modulators reveals a conformational checkpoint in receptor biogenesis
-
Huang, Y. and Breitwieser, G. E. (2007) Rescue of calcium-sensing receptor mutants by allosteric modulators reveals a conformational checkpoint in receptor biogenesis J. Biol. Chem. 282, 9517-9525
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 9517-9525
-
-
Huang, Y.1
Breitwieser, G.E.2
-
37
-
-
62149094752
-
The relative activity of "function sparing" HIV-1 entry inhibitors on viral entry and CCR5 internalization: Is allosteric functional selectivity a valuable therapeutic property?
-
Muniz-Medina, V. M., Jones, S., Maglich, J. M., Galardi, C., Hollingsworth, R. E., Kazmierski, W. M., Ferris, R. G., Edelstein, M. P., Chiswell, K. E., and Kenakin, T. P. (2009) The relative activity of "function sparing" HIV-1 entry inhibitors on viral entry and CCR5 internalization: is allosteric functional selectivity a valuable therapeutic property? Mol. Pharmacol. 75, 490-501
-
(2009)
Mol. Pharmacol.
, vol.75
, pp. 490-501
-
-
Muniz-Medina, V.M.1
Jones, S.2
Maglich, J.M.3
Galardi, C.4
Hollingsworth, R.E.5
Kazmierski, W.M.6
Ferris, R.G.7
Edelstein, M.P.8
Chiswell, K.E.9
Kenakin, T.P.10
-
38
-
-
0027240588
-
Differential signal transduction by five splice variants of the PACAP receptor
-
Spengler, D., Waeber, C., Pantaloni, C., Holsboer, F., Bockaert, J., Seeburg, P. H., and Journot, L. (1993) Differential signal transduction by five splice variants of the PACAP receptor Nature 365, 170-175
-
(1993)
Nature
, vol.365
, pp. 170-175
-
-
Spengler, D.1
Waeber, C.2
Pantaloni, C.3
Holsboer, F.4
Bockaert, J.5
Seeburg, P.H.6
Journot, L.7
-
39
-
-
47849101639
-
Location, location, location.site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling
-
Tobin, A. B., Butcher, A. J., and Kong, K. C. (2008) Location, location, location...site-specific GPCR phosphorylation offers a mechanism for cell-type-specific signalling Trends Pharmacol. Sci. 29, 413-420
-
(2008)
Trends Pharmacol. Sci.
, vol.29
, pp. 413-420
-
-
Tobin, A.B.1
Butcher, A.J.2
Kong, K.C.3
-
40
-
-
79953192547
-
Differential G-protein-coupled receptor phosphorylation provides evidence for a signaling bar code
-
Butcher, A. J., Prihandoko, R., Kong, K. C., McWilliams, P., Edwards, J. M., Bottrill, A., Mistry, S., and Tobin, A. B. (2011) Differential G-protein-coupled receptor phosphorylation provides evidence for a signaling bar code J. Biol. Chem. 286, 11506-11518
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 11506-11518
-
-
Butcher, A.J.1
Prihandoko, R.2
Kong, K.C.3
McWilliams, P.4
Edwards, J.M.5
Bottrill, A.6
Mistry, S.7
Tobin, A.B.8
-
41
-
-
80051616441
-
Distinct phosphorylation sites on the β(2)-adrenergic receptor establish a barcode that encodes differential functions of β-arrestin
-
Nobles, K. N., Xiao, K., Ahn, S., Shukla, A. K., Lam, C. M., Rajagopal, S., Strachan, R. T., Huang, T.-Y., Bressler, E. A., Hara, M. R., Shenoy, S. K., Gygi, S. P., and Lefkowitz, R. J. (2011) Distinct phosphorylation sites on the β(2)-adrenergic receptor establish a barcode that encodes differential functions of β-arrestin Sci. Signaling 4, ra51
-
(2011)
Sci. Signaling
, vol.4
, pp. 51
-
-
Nobles, K.N.1
Xiao, K.2
Ahn, S.3
Shukla, A.K.4
Lam, C.M.5
Rajagopal, S.6
Strachan, R.T.7
Huang, T.-Y.8
Bressler, E.A.9
Hara, M.R.10
Shenoy, S.K.11
Gygi, S.P.12
Lefkowitz, R.J.13
-
42
-
-
77951230331
-
Site-specific Phosphorylation of CXCR4 Is Dynamically Regulated by Multiple Kinases and Results in Differential Modulation of CXCR4 Signaling
-
Busillo, J., Armando, S., Sengupta, R., Meucci, O., Bouvier, M., and Benovic, J. (2010) Site-specific Phosphorylation of CXCR4 Is Dynamically Regulated by Multiple Kinases and Results in Differential Modulation of CXCR4 Signaling J. Biol. Chem. 285, 7805-7817
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 7805-7817
-
-
Busillo, J.1
Armando, S.2
Sengupta, R.3
Meucci, O.4
Bouvier, M.5
Benovic, J.6
-
43
-
-
67649856866
-
Selective engagement of G protein coupled receptor kinases (GRKs) encodes distinct functions of biased ligands
-
Zidar, D. A., Violin, J. D., Whalen, E. J., and Lefkowitz, R. J. (2009) Selective engagement of G protein coupled receptor kinases (GRKs) encodes distinct functions of biased ligands Proc. Natl. Acad. Sci. U.S.A. 106, 9649-9654
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 9649-9654
-
-
Zidar, D.A.1
Violin, J.D.2
Whalen, E.J.3
Lefkowitz, R.J.4
-
44
-
-
0033555946
-
Src-mediated tyrosine phosphorylation of dynamin is required for beta2-adrenergic receptor internalization and mitogen-activated protein kinase signaling
-
Ahn, S., Maudsley, S., Luttrell, L. M., Lefkowitz, R. J., and Daaka, Y. (1999) Src-mediated tyrosine phosphorylation of dynamin is required for beta2-adrenergic receptor internalization and mitogen-activated protein kinase signaling J. Biol. Chem. 274, 1185-1188
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 1185-1188
-
-
Ahn, S.1
Maudsley, S.2
Luttrell, L.M.3
Lefkowitz, R.J.4
Daaka, Y.5
-
45
-
-
0037088585
-
Beta-Arrestin scaffolding of the ERK cascade enhances cytosolic ERK activity but inhibits ERK-mediated transcription following angiotensin AT1a receptor stimulation
-
Tohgo, A., Pierce, K. L., Choy, E. W., Lefkowitz, R. J., and Luttrell, L. M. (2002) beta-Arrestin scaffolding of the ERK cascade enhances cytosolic ERK activity but inhibits ERK-mediated transcription following angiotensin AT1a receptor stimulation J. Biol. Chem. 277, 9429-9436
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 9429-9436
-
-
Tohgo, A.1
Pierce, K.L.2
Choy, E.W.3
Lefkowitz, R.J.4
Luttrell, L.M.5
-
46
-
-
36749094552
-
A unique mechanism of beta-blocker action: Carvedilol stimulates beta-arrestin signaling
-
Wisler, J. W., DeWire, S. M., Whalen, E. J., Violin, J. D., Drake, M. T., Ahn, S., Shenoy, S. K., and Lefkowitz, R. J. (2007) A unique mechanism of beta-blocker action: carvedilol stimulates beta-arrestin signaling Proc. Natl. Acad. Sci. U.S.A. 104, 16657-16662
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 16657-16662
-
-
Wisler, J.W.1
Dewire, S.M.2
Whalen, E.J.3
Violin, J.D.4
Drake, M.T.5
Ahn, S.6
Shenoy, S.K.7
Lefkowitz, R.J.8
-
47
-
-
0141703263
-
Independent beta-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2
-
Wei, H., Ahn, S., Shenoy, S. K., Karnik, S. S., Hunyady, L., Luttrell, L. M., and Lefkowitz, R. J. (2003) Independent beta-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2 Proc. Natl. Acad. Sci. U.S.A. 100, 10782-10787
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 10782-10787
-
-
Wei, H.1
Ahn, S.2
Shenoy, S.K.3
Karnik, S.S.4
Hunyady, L.5
Luttrell, L.M.6
Lefkowitz, R.J.7
-
48
-
-
73949084919
-
A beta-arrestin-biased agonist of the parathyroid hormone receptor (PTH1R) promotes bone formation independent of G protein activation
-
Gesty-Palmer, D., Flannery, P., Yuan, L., Corsino, L., Spurney, R., Lefkowitz, R. J., and Luttrell, L. M. (2009) A beta-arrestin-biased agonist of the parathyroid hormone receptor (PTH1R) promotes bone formation independent of G protein activation Sci. Transl. Med. 1, 1ra1
-
(2009)
Sci. Transl. Med.
, vol.1
-
-
Gesty-Palmer, D.1
Flannery, P.2
Yuan, L.3
Corsino, L.4
Spurney, R.5
Lefkowitz, R.J.6
Luttrell, L.M.7
-
49
-
-
78650508127
-
M3-muscarinic receptor promotes insulin release via receptor phosphorylation/arrestin-dependent activation of protein kinase D1
-
Kong, K. C., Butcher, A. J., McWilliams, P., Jones, D., Wess, J., Hamdan, F. F., Werry, T., Rosethorne, E. M., Charlton, S. J., Munson, S. E., Cragg, H. A., Smart, A. D., and Tobin, A. B. (2010) M3-muscarinic receptor promotes insulin release via receptor phosphorylation/arrestin-dependent activation of protein kinase D1 Proc. Natl. Acad. Sci. U.S.A. 107, 21181-21186
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 21181-21186
-
-
Kong, K.C.1
Butcher, A.J.2
McWilliams, P.3
Jones, D.4
Wess, J.5
Hamdan, F.F.6
Werry, T.7
Rosethorne, E.M.8
Charlton, S.J.9
Munson, S.E.10
Cragg, H.A.11
Smart, A.D.12
Tobin, A.B.13
-
50
-
-
76249122645
-
GLP-1 mediates antiapoptotic effect by phosphorylating Bad through a beta-arrestin 1-mediated ERK1/2 activation in pancreatic beta-cells
-
Quoyer, J., Longuet, C., Broca, C., Linck, N., Costes, S., Varin, E., Bockaert, J., Bertrand, G., and Dalle, S. (2010) GLP-1 mediates antiapoptotic effect by phosphorylating Bad through a beta-arrestin 1-mediated ERK1/2 activation in pancreatic beta-cells J. Biol. Chem. 285, 1989-2002
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 1989-2002
-
-
Quoyer, J.1
Longuet, C.2
Broca, C.3
Linck, N.4
Costes, S.5
Varin, E.6
Bockaert, J.7
Bertrand, G.8
Dalle, S.9
-
51
-
-
51649084026
-
Antagonism of dopamine D2 receptor/beta-arrestin 2 interaction is a common property of clinically effective antipsychotics
-
Masri, B., Salahpour, A., Didriksen, M., Ghisi, V., Beaulieu, J.-M., Gainetdinov, R. R., and Caron, M. G. (2008) Antagonism of dopamine D2 receptor/beta-arrestin 2 interaction is a common property of clinically effective antipsychotics Proc. Natl. Acad. Sci. U.S.A. 105, 13656-13661
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 13656-13661
-
-
Masri, B.1
Salahpour, A.2
Didriksen, M.3
Ghisi, V.4
Beaulieu, J.-M.5
Gainetdinov, R.R.6
Caron, M.G.7
-
52
-
-
66449111715
-
Beta-Arrestin1 mediates nicotinic acid-induced flushing, but not its antilipolytic effect, in mice
-
Walters, R. W., Shukla, A. K., Kovacs, J. J., Violin, J. D., DeWire, S. M., Lam, C. M., Chen, J. R., Muehlbauer, M. J., Whalen, E. J., and Lefkowitz, R. J. (2009) beta-Arrestin1 mediates nicotinic acid-induced flushing, but not its antilipolytic effect, in mice J. Clin. Invest. 119, 1312-1321
-
(2009)
J. Clin. Invest.
, vol.119
, pp. 1312-1321
-
-
Walters, R.W.1
Shukla, A.K.2
Kovacs, J.J.3
Violin, J.D.4
Dewire, S.M.5
Lam, C.M.6
Chen, J.R.7
Muehlbauer, M.J.8
Whalen, E.J.9
Lefkowitz, R.J.10
-
53
-
-
0036895747
-
Differential mechanisms of morphine antinociceptive tolerance revealed in (beta)arrestin-2 knock-out mice
-
Bohn, L. M., Lefkowitz, R. J., and Caron, M. G. (2002) Differential mechanisms of morphine antinociceptive tolerance revealed in (beta)arrestin-2 knock-out mice J. Neurosci. 22, 10494-10500
-
(2002)
J. Neurosci.
, vol.22
, pp. 10494-10500
-
-
Bohn, L.M.1
Lefkowitz, R.J.2
Caron, M.G.3
-
54
-
-
79956302829
-
Cellular Morphine Tolerance Produced by Arrestin-2-Dependent Impairment of -Opioid Receptor Resensitization
-
Dang, V. C., Chieng, B., Azriel, Y., and Christie, M. J. (2011) Cellular Morphine Tolerance Produced by Arrestin-2-Dependent Impairment of -Opioid Receptor Resensitization J. Neurosci. 31, 7122-7130
-
(2011)
J. Neurosci.
, vol.31
, pp. 7122-7130
-
-
Dang, V.C.1
Chieng, B.2
Azriel, Y.3
Christie, M.J.4
-
55
-
-
80053588007
-
Functional selectivity at the μ-opioid receptor: Implications for understanding opioid analgesia and tolerance
-
Raehal, K. M., Schmid, C. L., Groer, C. E., and Bohn, L. M. (2011) Functional selectivity at the μ-opioid receptor: implications for understanding opioid analgesia and tolerance Pharmacol. Rev. 63, 1001-1019
-
(2011)
Pharmacol. Rev.
, vol.63
, pp. 1001-1019
-
-
Raehal, K.M.1
Schmid, C.L.2
Groer, C.E.3
Bohn, L.M.4
-
56
-
-
80052416572
-
Agonist-directed interactions with specific arrestins determine μ-opioid receptor trafficking, ubiquitination, and dephosphorylation
-
Groer, C. E., Schmid, C. L., Jaeger, A. M., and Bohn, L. M. (2011) Agonist-directed interactions with specific arrestins determine μ-opioid receptor trafficking, ubiquitination, and dephosphorylation J. Biol. Chem. 286, 31731-31741
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 31731-31741
-
-
Groer, C.E.1
Schmid, C.L.2
Jaeger, A.M.3
Bohn, L.M.4
-
57
-
-
79957663678
-
Ligand-dependent mechanisms of sst2A receptor trafficking: Role of site-specific phosphorylation and receptor activation in the actions of biased somatostatin agonists
-
Kao, Y. J., Ghosh, M., and Schonbrunn, A. (2011) Ligand-dependent mechanisms of sst2A receptor trafficking: role of site-specific phosphorylation and receptor activation in the actions of biased somatostatin agonists Mol. Endocrinol. 25, 1040-1054
-
(2011)
Mol. Endocrinol.
, vol.25
, pp. 1040-1054
-
-
Kao, Y.J.1
Ghosh, M.2
Schonbrunn, A.3
-
58
-
-
84856068852
-
Functional selectivity in CB(2) cannabinoid receptor signaling and regulation: Implications for the therapeutic potential of CB(2) ligands
-
Atwood, B. K., Wager-Miller, J., Haskins, C., Straiker, A., and Mackie, K. (2012) Functional selectivity in CB(2) cannabinoid receptor signaling and regulation: implications for the therapeutic potential of CB(2) ligands Mol. Pharmacol. 81, 250-263
-
(2012)
Mol. Pharmacol.
, vol.81
, pp. 250-263
-
-
Atwood, B.K.1
Wager-Miller, J.2
Haskins, C.3
Straiker, A.4
MacKie, K.5
-
59
-
-
34447632041
-
Allosteric GPCR modulators: Taking advantage of permissive receptor pharmacology
-
Leach, K., Sexton, P., and Christopoulos, A. (2007) Allosteric GPCR modulators: taking advantage of permissive receptor pharmacology Trends Pharmacol. Sci. 28, 382-389
-
(2007)
Trends Pharmacol. Sci.
, vol.28
, pp. 382-389
-
-
Leach, K.1
Sexton, P.2
Christopoulos, A.3
-
60
-
-
26844448531
-
Allosteric modulators affect the internalization of human adenosine A1 receptors
-
Klaasse, E., den Hout, van, G., Roerink, S., de Grip, W., Ijzerman, A., and Beukers, M. (2005) Allosteric modulators affect the internalization of human adenosine A1 receptors Eur. J. Pharmacol. 522, 1-8
-
(2005)
Eur. J. Pharmacol.
, vol.522
, pp. 1-8
-
-
Klaasse, E.1
Den Van Hout, G.2
Roerink, S.3
De Grip, W.4
Ijzerman, A.5
Beukers, M.6
-
61
-
-
0029895280
-
Effects of long-term treatment with the allosteric enhancer, PD81,723, on Chinese hamster ovary cells expressing recombinant human A1 adenosine receptors
-
Bhattacharya, S. and Linden, J. (1996) Effects of long-term treatment with the allosteric enhancer, PD81,723, on Chinese hamster ovary cells expressing recombinant human A1 adenosine receptors Mol. Pharmacol. 50, 104-111
-
(1996)
Mol. Pharmacol.
, vol.50
, pp. 104-111
-
-
Bhattacharya, S.1
Linden, J.2
-
62
-
-
79955555416
-
Rescue of expression and signaling of human luteinizing hormone G protein-coupled receptor mutants with an allosterically binding small-molecule agonist
-
Newton, C. L., Whay, A. M., McArdle, C. A., Zhang, M., van Koppen, C. J., van de Lagemaat, R., Segaloff, D. L., and Millar, R. P. (2011) Rescue of expression and signaling of human luteinizing hormone G protein-coupled receptor mutants with an allosterically binding small-molecule agonist Proc. Natl. Acad. Sci. U.S.A. 108, 7172-7176
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
, pp. 7172-7176
-
-
Newton, C.L.1
Whay, A.M.2
McArdle, C.A.3
Zhang, M.4
Van Koppen, C.J.5
Van De Lagemaat, R.6
Segaloff, D.L.7
Millar, R.P.8
-
63
-
-
84860855040
-
Pharmacological characterization of a small-molecule agonist for the chemokine receptor CXCR3
-
Scholten, D. J., Canals, M., Wijtmans, M., de Munnik, S., Nguyen, P., Verzijl, D., de Esch, I. J. P., Vischer, H. F., Smit, M. J., and Leurs, R. (2012) Pharmacological characterization of a small-molecule agonist for the chemokine receptor CXCR3 Br. J. Pharmacol. 166, 898-911
-
(2012)
Br. J. Pharmacol.
, vol.166
, pp. 898-911
-
-
Scholten, D.J.1
Canals, M.2
Wijtmans, M.3
De Munnik, S.4
Nguyen, P.5
Verzijl, D.6
De Esch, I.J.P.7
Vischer, H.F.8
Smit, M.J.9
Leurs, R.10
-
64
-
-
0037428443
-
Identification of allosteric peptide agonists of CXCR4
-
Sachpatzidis, A., Benton, B. K., Manfredi, J. P., Wang, H., Hamilton, A., Dohlman, H. G., and Lolis, E. (2003) Identification of allosteric peptide agonists of CXCR4 J. Biol. Chem. 278, 896-907
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 896-907
-
-
Sachpatzidis, A.1
Benton, B.K.2
Manfredi, J.P.3
Wang, H.4
Hamilton, A.5
Dohlman, H.G.6
Lolis, E.7
|