메뉴 건너뛰기




Volumn 267, Issue 13, 2000, Pages 4253-4263

Conserved aromatic residues in the transmembrane region VI of the V(1a) vasopressin receptor differentiate agonist vs. antagonist ligand binding

Author keywords

Antagonist binding sites; Signal transduction; Site directed mutagenesis; Three dimensional model; Vasopressin receptors

Indexed keywords

VASOPRESSIN RECEPTOR;

EID: 0033944796     PISSN: 00142956     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1432-1033.2000.01472.x     Document Type: Article
Times cited : (62)

References (41)
  • 1
    • 0027933763 scopus 로고
    • Locating ligand-binding sites in 7TM receptors by protein engineering
    • 1. Schwartz, T.W. (1994) Locating ligand-binding sites in 7TM receptors by protein engineering. Curr. Opin. Biotechnol. 5, 434-444.
    • (1994) Curr. Opin. Biotechnol. , vol.5 , pp. 434-444
    • Schwartz, T.W.1
  • 3
    • 0032504237 scopus 로고    scopus 로고
    • G protein-coupled receptors. Diversity of receptor-ligand interactions
    • 3. Ji, T.H., Grossmann, M. & Ji, I. (1998) G protein-coupled receptors. Diversity of receptor-ligand interactions. J. Biol. Chem. 273, 17299-17302.
    • (1998) J. Biol. Chem. , vol.273 , pp. 17299-17302
    • Ji, T.H.1    Grossmann, M.2    Ji, I.3
  • 6
    • 0032061563 scopus 로고    scopus 로고
    • Molecular modeling of the human vasopressin V2 receptor/agonist complex
    • 6. Czaplewski, C., Kazmierkiewicz, R. & Ciarkowski, J. (1998) Molecular modeling of the human vasopressin V2 receptor/agonist complex. J. Comp.-Aid. Mol Design 12, 275-287.
    • (1998) J. Comp.-Aid. Mol Design , vol.12 , pp. 275-287
    • Czaplewski, C.1    Kazmierkiewicz, R.2    Ciarkowski, J.3
  • 8
    • 0028914070 scopus 로고
    • An extracellular residue determines the agonist specificity of V2 vasopressin receptors
    • 8. Ufer, E., Postina, R., Gorbulev, V. & Fahrenholz, F. (1995) An extracellular residue determines the agonist specificity of V2 vasopressin receptors. FEBS Lett. 362, 19-23.
    • (1995) FEBS Lett. , vol.362 , pp. 19-23
    • Ufer, E.1    Postina, R.2    Gorbulev, V.3    Fahrenholz, F.4
  • 9
    • 0032491601 scopus 로고    scopus 로고
    • Identification of residues responsible for the selective binding of peptide antagonists and agonists in the V2 vasopressin receptor
    • 9. Cotte, N., Balestre, M.N., Phalipou, S., Hibert, M., Manning, M., Barberis, C. & Mouillac, B. (1998) Identification of residues responsible for the selective binding of peptide antagonists and agonists in the V2 vasopressin receptor. J. Biol. Chem. 273, 29462-29468.
    • (1998) J. Biol. Chem. , vol.273 , pp. 29462-29468
    • Cotte, N.1    Balestre, M.N.2    Phalipou, S.3    Hibert, M.4    Manning, M.5    Barberis, C.6    Mouillac, B.7
  • 12
    • 0027532677 scopus 로고
    • Design, synthesis and some uses of receptor-specific agonists and antagonists of vasopressin and oxytocin
    • 12. Manning, M. & Sawyer, W.H. (1993) Design, synthesis and some uses of receptor-specific agonists and antagonists of vasopressin and oxytocin. J. Receptor Res. 13, 195-214.
    • (1993) J. Receptor Res. , vol.13 , pp. 195-214
    • Manning, M.1    Sawyer, W.H.2
  • 15
    • 0029905991 scopus 로고    scopus 로고
    • Separate agonist and peptide antagonist binding sites of the oxytocin receptor defined by their transfer into the V2 vasopressin receptor
    • 15. Postina, R., Kojro, E. & Fahrenholz, F. (1996) Separate agonist and peptide antagonist binding sites of the oxytocin receptor defined by their transfer into the V2 vasopressin receptor. J. Biol. Chem. 271, 31593-31601.
    • (1996) J. Biol. Chem. , vol.271 , pp. 31593-31601
    • Postina, R.1    Kojro, E.2    Fahrenholz, F.3
  • 16
    • 0031576219 scopus 로고    scopus 로고
    • Mapping peptide-binding domains of the human V1a vasopressin receptor with a photo-activatable linear peptide antagonist
    • 16. Phalipou, S., Cotte, N., Carnazzi, E., Seyer, R., Mahé, E., Jard, S., Barberis, C. & Mouillac, B. (1997) Mapping peptide-binding domains of the human V1a vasopressin receptor with a photo-activatable linear peptide antagonist. J. Biol. Chem. 272, 26536-26544.
    • (1997) J. Biol. Chem. , vol.272 , pp. 26536-26544
    • Phalipou, S.1    Cotte, N.2    Carnazzi, E.3    Seyer, R.4    Mahé, E.5    Jard, S.6    Barberis, C.7    Mouillac, B.8
  • 17
    • 0033551670 scopus 로고    scopus 로고
    • Docking of linear peptide antagonists into the human V1a vasopressin receptor: Identification of binding domains by photoaffininty labeling
    • 17. Phalipou, S., Seyer, R., Cotte, N., Breton, C., Barberis, C., Hibert, M. & Mouillac, B. (1999) Docking of linear peptide antagonists into the human V1a vasopressin receptor: identification of binding domains by photoaffininty labeling. J. Biol. Chem. 274, 23316-23327.
    • (1999) J. Biol. Chem. , vol.274 , pp. 23316-23327
    • Phalipou, S.1    Seyer, R.2    Cotte, N.3    Breton, C.4    Barberis, C.5    Hibert, M.6    Mouillac, B.7
  • 18
    • 0018897308 scopus 로고
    • [1-(β-mercapto-β,β-cyclopentamethylenepropionic acid),2-(O-methyl)-tyrosine]arginine vasopressin and [1-(β-mercapto-β,β-cyclopentamethylenepropionic acid)]arginine vasopressin, two highly potent antagonists of the vasopressor response to arginine vasopressin
    • 18. Kruszynski, M., Lammek, B., Manning, M., Seto, J., Haldar, J. & Sawyer, W.H. (1980) [1-(β-mercapto-β,β-cyclopentamethylenepropionic acid),2-(O-methyl)-tyrosine]arginine vasopressin and [1-(β-mercapto-β,β-cyclopentamethylenepropionic acid)]arginine vasopressin, two highly potent antagonists of the vasopressor response to arginine vasopressin. J. Med. Chem. 23, 364-368.
    • (1980) J. Med. Chem. , vol.23 , pp. 364-368
    • Kruszynski, M.1    Lammek, B.2    Manning, M.3    Seto, J.4    Haldar, J.5    Sawyer, W.H.6
  • 20
    • 0025944832 scopus 로고
    • Conformation of [8-arginine]vasopressin and V1 antagonists in dimethyl sulfoxide solution derived from two-dimensional NMR spectroscopy and molecular dynamics simulation
    • 20. Schmidt, J.M., Ohlenschläger, O., Rüterjans, H., Grzonka, Z., Kojro, E., Pavo, I. & Fahrenholz, F. (1991) Conformation of [8-arginine]vasopressin and V1 antagonists in dimethyl sulfoxide solution derived from two-dimensional NMR spectroscopy and molecular dynamics simulation. Eur. J. Biochem. 201, 355-371.
    • (1991) Eur. J. Biochem. , vol.201 , pp. 355-371
    • Schmidt, J.M.1    Ohlenschläger, O.2    Rüterjans, H.3    Grzonka, Z.4    Kojro, E.5    Pavo, I.6    Fahrenholz, F.7
  • 25
    • 0032217226 scopus 로고    scopus 로고
    • The D136A mutation of the V2 vasopressin receptor induces a constitutive activity which permits discrimination between antagonists with partial agonist and inverse agonist activities
    • 25. Morin, D., Cotte, N., Balestre, M.N., Mouillac, B., Manning, M., Breton, C. & Barberis, C. (1998) The D136A mutation of the V2 vasopressin receptor induces a constitutive activity which permits discrimination between antagonists with partial agonist and inverse agonist activities. FEBS Lett. 441, 470-475.
    • (1998) FEBS Lett. , vol.441 , pp. 470-475
    • Morin, D.1    Cotte, N.2    Balestre, M.N.3    Mouillac, B.4    Manning, M.5    Breton, C.6    Barberis, C.7
  • 26
    • 0019061918 scopus 로고
    • Ligand: A versatile computerized approach for the characterization of ligand binding systems
    • 26. Munson, P.J. & Rodbard, D. (1980) Ligand: a versatile computerized approach for the characterization of ligand binding systems. Anal. Biochem. 107, 220-239.
    • (1980) Anal. Biochem. , vol.107 , pp. 220-239
    • Munson, P.J.1    Rodbard, D.2
  • 27
    • 0025881062 scopus 로고
    • Three-dimensional models of neurotransmitter G-binding protein-coupled receptors
    • 27. Hibert, M., Trumpp-Kallmeyer, S., Bruinvels, A. & Hoflack, J. (1991) Three-dimensional models of neurotransmitter G-binding protein-coupled receptors. Mol. Pharmacol. 40, 8-15.
    • (1991) Mol. Pharmacol. , vol.40 , pp. 8-15
    • Hibert, M.1    Trumpp-Kallmeyer, S.2    Bruinvels, A.3    Hoflack, J.4
  • 28
    • 0026660322 scopus 로고
    • Modeling of G protein-coupled receptors: Application to dopamine, adrenaline, serotonin, acetylcholine, and mammalian opsin receptors
    • 28. Trumpp-Kallmeyer, S., Hoflack, J., Bruinvels, A. & Hibert, M. (1992) Modeling of G protein-coupled receptors: application to dopamine, adrenaline, serotonin, acetylcholine, and mammalian opsin receptors. J. Med. Chem. 35, 3448-3462.
    • (1992) J. Med. Chem. , vol.35 , pp. 3448-3462
    • Trumpp-Kallmeyer, S.1    Hoflack, J.2    Bruinvels, A.3    Hibert, M.4
  • 29
    • 0027190359 scopus 로고
    • Projection structure of rhodopsin
    • 29. Schertler, G.F., Villa, C. & Henderson, R. (1993) Projection structure of rhodopsin. Nature 362, 770-772.
    • (1993) Nature , vol.362 , pp. 770-772
    • Schertler, G.F.1    Villa, C.2    Henderson, R.3
  • 30
    • 0000296856 scopus 로고
    • Development of vasopressor specific vasotocin analogues with prolonged effects
    • (Giralt, E. & Andreu, D., eds). ESCOM Science Publishers, Leiden, Germany
    • 30. Aurell, C.J., Bengtsson, B., Ekholm, K., Kasprzykowska, R., Nilsson, A., Persson, R., Trojnar, J., Abbe, M. & Melin, P. (1991) Development of vasopressor specific vasotocin analogues with prolonged effects. In Peptides (Giralt, E. & Andreu, D., eds), pp. 671-673. ESCOM Science Publishers, Leiden, Germany.
    • (1991) Peptides , pp. 671-673
    • Aurell, C.J.1    Bengtsson, B.2    Ekholm, K.3    Kasprzykowska, R.4    Nilsson, A.5    Persson, R.6    Trojnar, J.7    Abbe, M.8    Melin, P.9
  • 33
    • 0029937609 scopus 로고    scopus 로고
    • Role of aromatic transmembrane residues of the d-opioid receptor in ligand recognition
    • 33. Befort, K., Tabbara, L., Kling, D., Maigret, B. & Kieffer, B.L. (1996) Role of aromatic transmembrane residues of the d-opioid receptor in ligand recognition. J. Biol. Chem. 271, 10161-10168.
    • (1996) J. Biol. Chem. , vol.271 , pp. 10161-10168
    • Befort, K.1    Tabbara, L.2    Kling, D.3    Maigret, B.4    Kieffer, B.L.5
  • 34
    • 0029165752 scopus 로고
    • Identification of residues involved in ligand binding to the neurokinin-2 receptor
    • 34. Huang, R.-R.C., Vicario, P.P., Strader, C.D. & Fong, T.M. (1995) Identification of residues involved in ligand binding to the neurokinin-2 receptor. Biochemistry 34, 10048-10055.
    • (1995) Biochemistry , vol.34 , pp. 10048-10055
    • Huang, R.-R.C.1    Vicario, P.P.2    Strader, C.D.3    Fong, T.M.4
  • 36
    • 0023740863 scopus 로고
    • Conserved aspartic acid residues 79 and 113 of the β-adrenergic receptor have different roles in receptor function
    • 36. Strader, C.D., Sigal, I.S., Candelore, M.R., Rands, E., Hill, W.S. & Dixon, R.A.F. (1988) Conserved aspartic acid residues 79 and 113 of the β-adrenergic receptor have different roles in receptor function. J. Biol. Chem. 263, 10267-10271.
    • (1988) J. Biol. Chem. , vol.263 , pp. 10267-10271
    • Strader, C.D.1    Sigal, I.S.2    Candelore, M.R.3    Rands, E.4    Hill, W.S.5    Dixon, R.A.F.6
  • 37
    • 0027296745 scopus 로고
    • Amino acid substitutions at position 312 in the seventh hydrophobic segment of the β2-adrenergic modify ligand-binding selectivity
    • 37. Suryanarayana, S. & Kobilka, B.K. (1993) Amino acid substitutions at position 312 in the seventh hydrophobic segment of the β2-adrenergic modify ligand-binding selectivity. Mol. Pharmacol. 44, 111-114.
    • (1993) Mol. Pharmacol. , vol.44 , pp. 111-114
    • Suryanarayana, S.1    Kobilka, B.K.2
  • 38
    • 0032541084 scopus 로고    scopus 로고
    • G protein-coupled receptors. Mechanism of agonist activation
    • 38. Gether, U. & Kobilka, B.K. (1998) G protein-coupled receptors. Mechanism of agonist activation. J. Biol. Chem. 273, 17979-17982.
    • (1998) J. Biol. Chem. , vol.273 , pp. 17979-17982
    • Gether, U.1    Kobilka, B.K.2
  • 39
    • 0029832901 scopus 로고    scopus 로고
    • Transmembrane regions V and VI of the luteinizing hormone receptor are required for constitutive activation by a mutation in the third intracellular loop
    • 39. Kudo, M., Osuga, Y., Kobilka, B.K. & Hsueh, A.J.W. (1996) Transmembrane regions V and VI of the luteinizing hormone receptor are required for constitutive activation by a mutation in the third intracellular loop. J. Biol. Chem. 271, 22470-22478.
    • (1996) J. Biol. Chem. , vol.271 , pp. 22470-22478
    • Kudo, M.1    Osuga, Y.2    Kobilka, B.K.3    Hsueh, A.J.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.