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Volumn 51, Issue 23, 2012, Pages 4685-4692

Conantokins derived from the Asprella clade impart con Rl-B, an N-methyl d-aspartate receptor antagonist with a unique selectivity profile for NR2B subunits

Author keywords

[No Author keywords available]

Indexed keywords

AMINO GROUP; ANTIEPILEPTIC DRUGS; CHEMICAL SYNTHESIS; CLINICAL APPLICATION; CONE SNAILS; D-ASPARTATE; DIVALENT METAL ION; HELICAL CONFORMATION; HIGH POTENCY; ION CHANNEL; MOLECULAR PHYLOGENY; NATURAL PRODUCTS; NMDA RECEPTOR; PEPTIDIC LIGANDS; POTENTIAL TARGETS; RECEPTOR ANTAGONISTS; SEQUENCE SIMILARITY; STRUCTURE-ACTIVITY STUDIES;

EID: 84862202566     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi300055n     Document Type: Article
Times cited : (15)

References (55)
  • 1
    • 0032914455 scopus 로고    scopus 로고
    • Antagonists selective for NMDA receptors containing the NR2B subunit
    • Chenard, B. L. and Menniti, F. S. (1999) Antagonists selective for NMDA receptors containing the NR2B subunit Curr. Pharm. Des. 5, 381-404 (Pubitemid 29238998)
    • (1999) Current Pharmaceutical Design , vol.5 , Issue.5 , pp. 381-404
    • Chenard, B.L.1    Menniti, F.S.2
  • 2
    • 0035577313 scopus 로고    scopus 로고
    • NMDA receptor antagonists as analgesics: Focus on the NR2B subtype
    • DOI 10.1016/S0165-6147(00)01863-0, PII S0165614700018630
    • Chizh, B. A., Headley, P. M., and Tzschentke, T. M. (2001) NMDA receptor antagonists as analgesics: Focus on the NR2B subtype Trends Pharmacol. Sci. 22, 636-642 (Pubitemid 33135525)
    • (2001) Trends in Pharmacological Sciences , vol.22 , Issue.12 , pp. 636-642
    • Chizh, B.A.1    Headley P.Max2    Tzschentke, T.M.3
  • 7
    • 70350452578 scopus 로고    scopus 로고
    • N-Methyl- d -aspartate (NMDA) receptor NR2 subunit selectivity of a series of novel piperazine-2,3-dicarboxylate derivatives: Preferential blockade of extrasynaptic NMDA receptors in the rat hippocampal CA3-CA1 synapse
    • Costa, B. M., Feng, B., Tsintsadze, T. S., Morley, R. M., Irvine, M. W., Tsintsadze, V., Lozovaya, N. A., Jane, D. E., and Monaghan, D. T. (2009) N-Methyl- d -aspartate (NMDA) receptor NR2 subunit selectivity of a series of novel piperazine-2,3-dicarboxylate derivatives: Preferential blockade of extrasynaptic NMDA receptors in the rat hippocampal CA3-CA1 synapse J. Pharmacol. Exp. Ther. 331, 618-626
    • (2009) J. Pharmacol. Exp. Ther. , vol.331 , pp. 618-626
    • Costa, B.M.1    Feng, B.2    Tsintsadze, T.S.3    Morley, R.M.4    Irvine, M.W.5    Tsintsadze, V.6    Lozovaya, N.A.7    Jane, D.E.8    Monaghan, D.T.9
  • 8
    • 1542269774 scopus 로고    scopus 로고
    • Structure - Activity analysis of a novel NR2C/NR2D-preferring NMDA receptor antagonist: 1-(phenanthrene-2-carbonyl) piperazine-2,3-dicarboxylic acid
    • DOI 10.1038/sj.bjp.0705644
    • Feng, B., Tse, H. W., Skifter, D. A., Morley, R., Jane, D. E., and Monaghan, D. T. (2004) Structure-activity analysis of a novel NR2C/NR2D-preferring NMDA receptor antagonist: 1-(Phenanthrene-2-carbonyl) piperazine-2,3-dicarboxylic acid Br. J. Pharmacol. 141, 508-516 (Pubitemid 38297013)
    • (2004) British Journal of Pharmacology , vol.141 , Issue.3 , pp. 508-516
    • Feng, B.1    Tse, H.W.2    Skifter, D.A.3    Morley, R.4    Jane, D.E.5    Monaghan, D.T.6
  • 10
    • 17144378207 scopus 로고    scopus 로고
    • 1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists
    • DOI 10.1021/jm0492498
    • Morley, R. M., Tse, H. W., Feng, B., Miller, J. C., Monaghan, D. T., and Jane, D. E. (2005) Synthesis and pharmacology of N1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists J. Med. Chem. 48, 2627-2637 (Pubitemid 40516452)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.7 , pp. 2627-2637
    • Morley, R.M.1    Tse, H.-W.2    Feng, B.3    Miller, J.C.4    Monaghan, D.T.5    Jane, D.E.6
  • 11
    • 0032478159 scopus 로고    scopus 로고
    • 5-Aminomethylquinoxaline-2,3-diones, Part III: Arylamide derivatives as highly potent and selective glycine-site NMDA receptor antagonists
    • DOI 10.1016/S0960-894X(98)00055-9, PII S0960894X98000559
    • Acklin, P., Allgeier, H., Auberson, Y. P., Bischoff, S., Ofner, S., Sauer, D., and Schmutz, M. (1998) 5-Aminomethylquinoxaline-2,3-diones, Part III: Arylamide derivatives as highly potent and selective glycine-site NMDA receptor antagonists Bioorg. Med. Chem. Lett. 8, 493-498 (Pubitemid 28092381)
    • (1998) Bioorganic and Medicinal Chemistry Letters , vol.8 , Issue.5 , pp. 493-498
    • Acklin, P.1    Allgeier, H.2    Auberson, Y.P.3    Bischoff, S.4    Ofner, S.5    Sauer, D.6    Schmutz, M.7
  • 12
    • 0034598310 scopus 로고    scopus 로고
    • Synthesis, radiolabelling and biological characterization of (D)-7-iodo- N-(1-phosphonoethyl)-5-aminomethylquinoxaline-2,3-dione, a glycine-binding site antagonist of NMDA receptors
    • DOI 10.1016/S0960-894X(99)00576-4, PII S0960894X99005764
    • Ametamey, S. M., Kokic, M., Carrey-Remy, N., Blauenstein, P., Willmann, M., Bischoff, S., Schmutz, M., Schubiger, P. A., and Auberson, Y. P. (2000) Synthesis, radiolabelling and biological characterization of d -7-iodo-N-(1-phosphonoethyl)-5-aminomethylquinoxaline-2,3-dione, a glycine-binding site antagonist of NMDA receptors Bioorg. Med. Chem. Lett. 10, 75-78 (Pubitemid 30014675)
    • (2000) Bioorganic and Medicinal Chemistry Letters , vol.10 , Issue.1 , pp. 75-78
    • Ametamey, S.M.1    Kokic, M.2    Carrey-Remy, N.3    Blauenstein, P.4    Willmann, M.5    Bischoff, S.6    Schmutz, M.7    Schubiger, P.A.8    Auberson, Y.P.9
  • 14
    • 0037041183 scopus 로고    scopus 로고
    • 5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition
    • DOI 10.1016/S0960-894X(02)00074-4, PII S0960894X02000744
    • Auberson, Y. P., Allgeier, H., Bischoff, S., Lingenhoehl, K., Moretti, R., and Schmutz, M. (2002) 5-Phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition Bioorg. Med. Chem. Lett. 12, 1099-1102 (Pubitemid 34242811)
    • (2002) Bioorganic and Medicinal Chemistry Letters , vol.12 , Issue.7 , pp. 1099-1102
    • Auberson, Y.P.1    Allgeier, H.2    Bischoff, S.3    Lingenhoehl, K.4    Moretti, R.5    Schmutz, M.6
  • 15
    • 9144236304 scopus 로고    scopus 로고
    • Conantokins: Peptide antagonists of NMDA receptors
    • Layer, R. T., Wagstaff, J. D., and White, H. S. (2004) Conantokins: Peptide antagonists of NMDA receptors Curr. Med. Chem. 11, 3073-3084 (Pubitemid 39545576)
    • (2004) Current Medicinal Chemistry , vol.11 , Issue.23 , pp. 3073-3084
    • Layer, R.T.1    Wagstaff, J.D.2    White, H.S.3
  • 16
    • 34249010244 scopus 로고    scopus 로고
    • The molecular basis of Conantokin antagonism of NMDA receptor function
    • DOI 10.2174/138945007780618481
    • Prorok, M. and Castellino, F. J. (2007) The molecular basis of conantokin antagonism of NMDA receptor function Curr. Drug Targets 8, 633-642 (Pubitemid 46785061)
    • (2007) Current Drug Targets , vol.8 , Issue.5 , pp. 633-642
    • Prorok, M.1    Castellino, F.J.2
  • 17
    • 0033851790 scopus 로고    scopus 로고
    • Conantokin G is an NR2B-selective competitive antagonist of N-methyl- d -aspartate receptors
    • Donevan, S. D. and McCabe, R. T. (2000) Conantokin G is an NR2B-selective competitive antagonist of N-methyl- d -aspartate receptors Mol. Pharmacol. 58, 614-623
    • (2000) Mol. Pharmacol. , vol.58 , pp. 614-623
    • Donevan, S.D.1    McCabe, R.T.2
  • 18
    • 34547211472 scopus 로고    scopus 로고
    • Subtype-selective antagonism of N-methyl-d-aspartate receptor ion channels by synthetic conantokin peptides
    • DOI 10.1016/j.neuropharm.2007.04.016, PII S0028390807001244
    • Sheng, Z., Dai, Q., Prorok, M., and Castellino, F. J. (2007) Subtype-selective antagonism of N-methyl- d -aspartate receptor ion channels by synthetic conantokin peptides Neuropharmacology 53, 145-156 (Pubitemid 47125955)
    • (2007) Neuropharmacology , vol.53 , Issue.1 , pp. 145-156
    • Sheng, Z.1    Dai, Q.2    Prorok, M.3    Castellino, F.J.4
  • 19
    • 67650125196 scopus 로고    scopus 로고
    • The selectivity of conantokin-G for ion channel inhibition of NR2B subunit-containing NMDA receptors is regulated by amino acid residues in the S2 region of NR2B
    • Sheng, Z., Liang, Z., Geiger, J. H., Prorok, M., and Castellino, F. J. (2009) The selectivity of conantokin-G for ion channel inhibition of NR2B subunit-containing NMDA receptors is regulated by amino acid residues in the S2 region of NR2B Neuropharmacology 57, 127-136
    • (2009) Neuropharmacology , vol.57 , pp. 127-136
    • Sheng, Z.1    Liang, Z.2    Geiger, J.H.3    Prorok, M.4    Castellino, F.J.5
  • 20
    • 79953236709 scopus 로고    scopus 로고
    • Specific determinants of conantokins that dictate their selectivity for the NR2B subunit of N-methyl- d -aspartate receptors
    • Sheng, Z., Prorok, M., and Castellino, F. J. (2010) Specific determinants of conantokins that dictate their selectivity for the NR2B subunit of N-methyl- d -aspartate receptors Neuroscience 170, 703-710
    • (2010) Neuroscience , vol.170 , pp. 703-710
    • Sheng, Z.1    Prorok, M.2    Castellino, F.J.3
  • 21
    • 62149122662 scopus 로고    scopus 로고
    • Neuroprotective and cardioprotective conopeptides: An emerging class of drug leads
    • Twede, V. D., Miljanich, G., Olivera, B. M., and Bulaj, G. (2009) Neuroprotective and cardioprotective conopeptides: An emerging class of drug leads Curr. Opin. Drug Discovery Dev. 12, 231-239
    • (2009) Curr. Opin. Drug Discovery Dev. , vol.12 , pp. 231-239
    • Twede, V.D.1    Miljanich, G.2    Olivera, B.M.3    Bulaj, G.4
  • 22
  • 23
    • 56349135882 scopus 로고    scopus 로고
    • NR2B-selective conantokin peptide inhibitors of the NMDA receptor display enhanced antinociceptive properties compared to non-selective conantokins
    • Xiao, C., Huang, Y., Dong, M., Hu, J., Hou, S., Castellino, F. J., Prorok, M., and Dai, Q. (2008) NR2B-selective conantokin peptide inhibitors of the NMDA receptor display enhanced antinociceptive properties compared to non-selective conantokins Neuropeptides 42, 601-609
    • (2008) Neuropeptides , vol.42 , pp. 601-609
    • Xiao, C.1    Huang, Y.2    Dong, M.3    Hu, J.4    Hou, S.5    Castellino, F.J.6    Prorok, M.7    Dai, Q.8
  • 24
    • 0037219288 scopus 로고    scopus 로고
    • Powerful antinociceptive effects of the cone snail venom-derived subtype-selective NMDA receptor antagonists conantokins G and T
    • DOI 10.1016/S0304-3959(02)00303-2
    • Malmberg, A. B., Gilbert, H., McCabe, R. T., and Basbaum, A. I. (2003) Powerful antinociceptive effects of the cone snail venom-derived subtype-selective NMDA receptor antagonists conantokins G and T Pain 101, 109-116 (Pubitemid 36044658)
    • (2003) Pain , vol.101 , Issue.1-2 , pp. 109-116
    • Malmberg, A.B.1    Gilbert, H.2    McCabe, R.T.3    Basbaum, A.I.4
  • 25
    • 58549085757 scopus 로고    scopus 로고
    • Antinociceptive effects of the marine snail peptides conantokin-G and conotoxin MVIIA alone and in combination in rat models of pain
    • Hama, A. and Sagen, J. (2009) Antinociceptive effects of the marine snail peptides conantokin-G and conotoxin MVIIA alone and in combination in rat models of pain Neuropharmacology 56, 556-563
    • (2009) Neuropharmacology , vol.56 , pp. 556-563
    • Hama, A.1    Sagen, J.2
  • 26
    • 2342649960 scopus 로고    scopus 로고
    • The effect of CGX-1007 and CI-1041, novel NMDA receptor antagonists, on NMDA receptor-mediated EPSCs
    • DOI 10.1016/j.eplepsyres.2003.12.011, PII S0920121104000506
    • Barton, M. E., White, H. S., and Wilcox, K. S. (2004) The effect of CGX-1007 and CI-1041, novel NMDA receptor antagonists, on NMDA receptor-mediated EPSCs Epilepsy Res. 59, 13-24 (Pubitemid 38595417)
    • (2004) Epilepsy Research , vol.59 , Issue.1 , pp. 13-24
    • Barton, M.E.1    White, H.S.2    Wilcox, K.S.3
  • 27
    • 0036146487 scopus 로고    scopus 로고
    • New antiepileptic drugs currently in clinical trials: Is there a strategy in their development?
    • DOI 10.1097/00007691-200202000-00015
    • Bialer, M. (2002) New antiepileptic drugs currently in clinical trials: Is there a strategy in their development? Ther. Drug Monit. 24, 85-90 (Pubitemid 34106737)
    • (2002) Therapeutic Drug Monitoring , vol.24 , Issue.1 , pp. 85-90
    • Bialer, M.1
  • 28
    • 0036752811 scopus 로고    scopus 로고
    • Progress report on new antiepileptic drugs: A summary of the Sixth Eilat Conference (EILAT VI)
    • DOI 10.1016/S0920-1211(02)00106-7, PII S0920121102001067
    • Bialer, M., Johannessen, S. I., Kupferberg, H. J., Levy, R. H., Loiseau, P., and Perucca, E. (2002) Progress report on new antiepileptic drugs: A summary of the Sixth Eilat Conference (EILAT VI) Epilepsy Res. 51, 31-71 (Pubitemid 35283878)
    • (2002) Epilepsy Research , vol.51 , Issue.1-2 , pp. 31-71
    • Bialer, M.1    Johannessen, S.I.2    Kupferberg, H.J.3    Levy, R.H.4    Loiseau, P.5    Perucca, E.6
  • 29
    • 52949118506 scopus 로고    scopus 로고
    • Conus Venoms: A Rich Source of Peptide-Based Therapeutics
    • Han, T. S., Teichert, R. W., Olivera, B. M., and Bulaj, G. (2008) Conus Venoms: A Rich Source of Peptide-Based Therapeutics Curr. Pharm. Des. 14, 2462-2479
    • (2008) Curr. Pharm. Des. , vol.14 , pp. 2462-2479
    • Han, T.S.1    Teichert, R.W.2    Olivera, B.M.3    Bulaj, G.4
  • 30
    • 33845992556 scopus 로고    scopus 로고
    • Conus peptides: Biodiversity-based discovery and exogenomics
    • DOI 10.1074/jbc.R600020200
    • Olivera, B. M. (2006) Conus peptides: Biodiversity-based discovery and exogenomics J. Biol. Chem. 281, 31173-31177 (Pubitemid 46041381)
    • (2006) Journal of Biological Chemistry , vol.281 , Issue.42 , pp. 31173-31177
    • Olivera, B.M.1
  • 31
    • 77953391048 scopus 로고    scopus 로고
    • Natural products and ion channel pharmacology
    • Teichert, R. W. and Olivera, B. M. (2010) Natural products and ion channel pharmacology Future Med. Chem. 2, 731-744
    • (2010) Future Med. Chem. , vol.2 , pp. 731-744
    • Teichert, R.W.1    Olivera, B.M.2
  • 33
    • 50449088156 scopus 로고    scopus 로고
    • Integrating the discovery pipeline for novel compounds targeting ion channels
    • Bulaj, G. (2008) Integrating the discovery pipeline for novel compounds targeting ion channels Curr. Opin. Chem. Biol. 12, 441-447
    • (2008) Curr. Opin. Chem. Biol. , vol.12 , pp. 441-447
    • Bulaj, G.1
  • 34
    • 37549069739 scopus 로고    scopus 로고
    • Novel Conantokins from Conus parius Venom Are Specific Antagonists of N-Methyl- d -aspartate Receptors
    • Teichert, R. W., Jimenez, E. C., Twede, V., Watkins, M., Hollmann, M., Bulaj, G., and Olivera, B. M. (2007) Novel Conantokins from Conus parius Venom Are Specific Antagonists of N-Methyl- d -aspartate Receptors J. Biol. Chem. 282, 36905-36913
    • (2007) J. Biol. Chem. , vol.282 , pp. 36905-36913
    • Teichert, R.W.1    Jimenez, E.C.2    Twede, V.3    Watkins, M.4    Hollmann, M.5    Bulaj, G.6    Olivera, B.M.7
  • 36
    • 77957300637 scopus 로고    scopus 로고
    • Characterization of conantokin Rl-A: Molecular phylogeny as structure/function study
    • Gowd, K. H., Watkins, M., Twede, V. D., Bulaj, G. W., and Olivera, B. M. (2010) Characterization of conantokin Rl-A: Molecular phylogeny as structure/function study J. Pept. Sci. 16, 375-382
    • (2010) J. Pept. Sci. , vol.16 , pp. 375-382
    • Gowd, K.H.1    Watkins, M.2    Twede, V.D.3    Bulaj, G.W.4    Olivera, B.M.5
  • 37
    • 0028169661 scopus 로고
    • Ligand affinities at recombinant N-methyl- d -aspartate receptors depend on subunit composition
    • Laurie, D. J. and Seeburg, P. H. (1994) Ligand affinities at recombinant N-methyl- d -aspartate receptors depend on subunit composition Eur. J. Pharmacol. 268, 335-345
    • (1994) Eur. J. Pharmacol. , vol.268 , pp. 335-345
    • Laurie, D.J.1    Seeburg, P.H.2
  • 38
    • 0028226884 scopus 로고
    • Regional and developmental heterogeneity in splicing of the rat brain NMDAR1 mRNA
    • Laurie, D. J. and Seeburg, P. H. (1994) Regional and developmental heterogeneity in splicing of the rat brain NMDAR1 mRNA J. Neurosci. 14, 3180-3194 (Pubitemid 24139002)
    • (1994) Journal of Neuroscience , vol.14 , Issue.5 , pp. 3180-3194
    • Laurie, D.J.1    Seeburg, P.H.2
  • 39
    • 0035920125 scopus 로고    scopus 로고
    • The amino acid residue at sequence position 5 in the conantokin peptides partially governs subunit-selective antagonism of recombinant N-methyl- d -aspartate receptors
    • Klein, R. C., Prorok, M., Galdzicki, Z., and Castellino, F. J. (2001) The amino acid residue at sequence position 5 in the conantokin peptides partially governs subunit-selective antagonism of recombinant N-methyl- d -aspartate receptors J. Biol. Chem. 276, 26860-26867
    • (2001) J. Biol. Chem. , vol.276 , pp. 26860-26867
    • Klein, R.C.1    Prorok, M.2    Galdzicki, Z.3    Castellino, F.J.4
  • 40
    • 0034783460 scopus 로고    scopus 로고
    • Kinetic and mechanistic characterization of NMDA receptor antagonism by replacement and truncation variants of the conantokin peptides
    • DOI 10.1016/S0028-3908(01)00119-8, PII S0028390801001198
    • Klein, R. C., Warder, S. E., Galdzicki, Z., Castellino, F. J., and Prorok, M. (2001) Kinetic and mechanistic characterization of NMDA receptor antagonism by replacement and truncation variants of the conantokin peptides Neuropharmacology 41, 801-810 (Pubitemid 33001414)
    • (2001) Neuropharmacology , vol.41 , Issue.7 , pp. 801-810
    • Klein, R.C.1    Warder, S.E.2    Galdzicki, Z.3    Castellino, F.J.4    Prorok, M.5
  • 43
    • 0030449042 scopus 로고    scopus 로고
    • Calcium binding properties of synthetic γ-carboxyglutamic acid-containing marine cone snail "sleeper" peptides, conantokin-G and conantokin-T
    • Prorok, M., Warder, S. E., Blandl, T., and Castellino, F. J. (1996) Calcium binding properties of synthetic γ-carboxyglutamic acid-containing marine cone snail "sleeper" peptides, conantokin-G and conantokin-T Biochemistry 35, 16528-16534
    • (1996) Biochemistry , vol.35 , pp. 16528-16534
    • Prorok, M.1    Warder, S.E.2    Blandl, T.3    Castellino, F.J.4
  • 44
    • 0032797897 scopus 로고    scopus 로고
    • Calcium binding mode of gamma-carboxyglutamic acids in conantokins
    • Lin, C. H., Chan, F. C., Hwang, J. K., and Lyu, P. C. (1999) Calcium binding mode of γ-carboxyglutamic acids in conantokins Protein Eng. 12, 589-595 (Pubitemid 29368966)
    • (1999) Protein Engineering , vol.12 , Issue.7 , pp. 589-595
    • Lin, C.H.1    Chan, F.C.H.2    Hwang, J.K.3    Lyu, P.C.4
  • 45
    • 0031456675 scopus 로고    scopus 로고
    • Role of gamma-carboxyglutamic acid in the calcium-induced structural transition of conantokin G, a conotoxin from the marine snail Conus geographus
    • DOI 10.1021/bi9718550
    • Rigby, A. C., Baleja, J. D., Li, L., Pedersen, L. G., Furie, B. C., and Furie, B. (1997) Role of γ-carboxyglutamic acid in the calcium-induced structural transition of conantokin G, a conotoxin from the marine snail Conus geographus Biochemistry 36, 15677-15684 (Pubitemid 28027366)
    • (1997) Biochemistry , vol.36 , Issue.50 , pp. 15677-15684
    • Rigby, A.C.1    Baleja, J.D.2    Li, L.3    Pedersen, L.G.4    Furie, B.C.5    Furie, B.6
  • 46
    • 0032568831 scopus 로고    scopus 로고
    • Conformational changes in conantokin-G induced upon binding of calcium and magnesium as revealed by NMR structural analysis
    • DOI 10.1074/jbc.273.26.16248
    • Chen, Z., Blandl, T., Prorok, M., Warder, S. E., Li, L., Zhu, Y., Pedersen, L. G., Ni, F., and Castellino, F. J. (1998) Conformational changes in conantokin-G induced upon binding of calcium and magnesium as revealed by NMR structural analysis J. Biol. Chem. 273, 16248-16258 (Pubitemid 28311401)
    • (1998) Journal of Biological Chemistry , vol.273 , Issue.26 , pp. 16248-16258
    • Chen, Z.1    Blandl, T.2    Prorok, M.3    Warder, S.E.4    Li, L.5    Zhu, Y.6    Pedersen, L.G.7    Ni, F.8    Castellino, F.J.9
  • 47
    • 33846961465 scopus 로고    scopus 로고
    • The crystal structures of the calcium-bound con-G and con-T[K7γ] dimeric peptides demonstrate a metal-dependent helix-forming motif
    • Cnudde, S. E., Prorok, M., Dai, Q., Castellino, F. J., and Geiger, J. H. (2007) The crystal structures of the calcium-bound con-G and con-T[K7γ] dimeric peptides demonstrate a metal-dependent helix-forming motif J. Am. Chem. Soc. 129, 1586-1593
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1586-1593
    • Cnudde, S.E.1    Prorok, M.2    Dai, Q.3    Castellino, F.J.4    Geiger, J.H.5
  • 48
    • 0034798601 scopus 로고    scopus 로고
    • Point mutations identify the glutamate binding pocket of the N-methyl-D-aspartate receptor as major site of Conantokin-G inhibition
    • DOI 10.1016/S0028-3908(01)00112-5, PII S0028390801001125
    • Wittekindt, B., Malany, S., Schemm, R., Otvos, L., Maccecchini, M. L., Laube, B., and Betz, H. (2001) Point mutations identify the glutamate binding pocket of the N-methyl- d -aspartate receptor as major site of conantokin-G inhibition Neuropharmacology 41, 753-761 (Pubitemid 32972193)
    • (2001) Neuropharmacology , vol.41 , Issue.6 , pp. 753-761
    • Wittekindt, B.1    Malany, S.2    Schemm, R.3    Otvos, L.4    Maccecchini, M.-L.5    Laube, B.6    Betz, H.7
  • 49
    • 79955099725 scopus 로고    scopus 로고
    • CGX-1007 prevents excitotoxic cell death via actions at multiple types of NMDA receptors
    • Alex, A. B., Saunders, G. W., Dalpe-Charron, A., Reilly, C. A., and Wilcox, K. S. (2011) CGX-1007 prevents excitotoxic cell death via actions at multiple types of NMDA receptors Neurotoxicology 32, 392-399
    • (2011) Neurotoxicology , vol.32 , pp. 392-399
    • Alex, A.B.1    Saunders, G.W.2    Dalpe-Charron, A.3    Reilly, C.A.4    Wilcox, K.S.5
  • 50
    • 33644837888 scopus 로고    scopus 로고
    • NMDA receptor subunit-dependent modulation by conantokin-G and Ala7-conantokin-G
    • Ragnarsson, L., Yasuda, T., Lewis, R. J., Dodd, P. R., and Adams, D. J. (2006) NMDA receptor subunit-dependent modulation by conantokin-G and Ala7-conantokin-G J. Neurochem. 96, 283-291
    • (2006) J. Neurochem. , vol.96 , pp. 283-291
    • Ragnarsson, L.1    Yasuda, T.2    Lewis, R.J.3    Dodd, P.R.4    Adams, D.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.