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Next Article 
The Journal of Neuroscience, January 15, 1998, 18(2):581-589
Identification of Amino Acid Residues of the NR2A Subunit That
Control Glutamate Potency in Recombinant NR1/NR2A NMDA
Receptors
Lesley C.
Anson1, 2,
Philip E.
Chen1, 2,
David J. A.
Wyllie2,
David
Colquhoun1, 2, and
Ralf
Schoepfer1, 2
University College London, 1 Wellcome Laboratory for
Molecular Pharmacology, and 2 Department of Pharmacology,
London WC1E 6BT, United Kingdom
The NMDA type of ligand-gated glutamate receptor requires the
presence of both glutamate and glycine for gating. These receptors are
hetero-oligomers of NR1 and NR2 subunits. Previously it was thought
that the binding sites for glycine and glutamate were formed by
residues on the NR1 subunit. Indeed, it has been shown that the effects
of glycine are controlled by residues on the NR1 subunit, and a
"Venus flytrap" model for the glycine binding site has been
suggested by analogy with bacterial periplasmic amino acid binding
proteins. By analysis of 10 mutant NMDA receptors, we now show that
residues on the NR2A subunit control glutamate potency in recombinant
NR1/NR2A receptors, without affecting glycine potency. Furthermore, we
provide evidence that, at least for some mutated residues, the reduced
potency of glutamate cannot be explained by alteration of gating but
has to be caused primarily by impairing the binding of the agonist to
the resting state of the receptor. One NR2A mutant, NR2A(T671A), had an
EC50 for glutamate 1000-fold greater than
wild type and a 255-fold reduced affinity for APV, yet it had
single-channel openings very similar to those of wild type. Therefore
we propose that the glutamate binding site is located on NR2 subunits
and (taking our data together with previous work) is not on the NR1
subunit. Our data further imply that each NMDA receptor subunit
possesses a binding site for an agonist (glutamate or glycine).
Key words:
N-methyl-D-aspartate (NMDA); glutamate; receptor; recombinant; subunit; ligand; binding; gating; single-channel; APV; Schild plot; affinity; oocyte; mutant; kinetic
Copyright © 1998 Society for Neuroscience 0270-6474/98/182581-09$05.00/0
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Glutamate But Not Glycine Agonist Affinity for NMDA Receptors Is Influenced by Small Cations
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K. S. Jones, H. M. A. VanDongen, and A. M. J. VanDongen
The NMDA Receptor M3 Segment Is a Conserved Transduction Element Coupling Ligand Binding to Channel Opening
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K. Kashiwagi, T. Masuko, C. D. Nguyen, T. Kuno, I. Tanaka, K. Igarashi, and K. Williams
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March 1, 2002;
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T. Green, C. A. Rogers, A. Contractor, and S. F. Heinemann
NMDA Receptors Formed by NR1 in Xenopus laevis Oocytes Do Not Contain the Endogenous Subunit XenU1
Mol. Pharmacol.,
February 1, 2002;
61(2):
326 - 333.
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Y.-B. Choi, H.-S. V. Chen, and S. A. Lipton
Three Pairs of Cysteine Residues Mediate Both Redox and Zn2+ Modulation of the NMDA Receptor
J. Neurosci.,
January 15, 2001;
21(2):
392 - 400.
[Abstract]
[Full Text]
[PDF]
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D. A. Wagner and C. Czajkowski
Structure and Dynamics of the GABA Binding Pocket: A Narrowing Cleft that Constricts during Activation
J. Neurosci.,
January 1, 2001;
21(1):
67 - 74.
[Abstract]
[Full Text]
[PDF]
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J. N. C. Kew, A. Koester, J.-L. Moreau, F. Jenck, A.-M. Ouagazzal, V. Mutel, J. G. Richards, G. Trube, G. Fischer, A. Montkowski, et al.
Functional Consequences of Reduction in NMDA Receptor Glycine Affinity in Mice Carrying Targeted Point Mutations in the Glycine Binding Site
J. Neurosci.,
June 1, 2000;
20(11):
4037 - 4049.
[Abstract]
[Full Text]
[PDF]
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J. M. Christie, D. E. Jane, and D. T. Monaghan
Native N-Methyl-D-aspartate Receptors Containing NR2A and NR2B Subunits Have Pharmacologically Distinct Competitive Antagonist Binding Sites
J. Pharmacol. Exp. Ther.,
March 1, 2000;
292(3):
1169 - 1174.
[Abstract]
[Full Text]
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A. I. Sobolevsky, S. G. Koshelev, and B. I. Khodorov
Probing of NMDA Channels with Fast Blockers
J. Neurosci.,
December 15, 1999;
19(24):
10611 - 10626.
[Abstract]
[Full Text]
[PDF]
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J. R. Howe
REVIEW {blacksquare} : How Glutamate Receptors Are Built
Neuroscientist,
September 1, 1999;
5(5):
311 - 323.
[Abstract]
[PDF]
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F. Conti, P. Barbaresi, M. Melone, and A. Ducati
Neuronal and Glial Localization of NR1 and NR2A/B Subunits of the NMDA Receptor in the Human Cerebral Cortex
Cereb Cortex,
March 1, 1999;
9(2):
110 - 120.
[Abstract]
[Full Text]
[PDF]
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R. Dingledine, K. Borges, D. Bowie, and S. F. Traynelis
The Glutamate Receptor Ion Channels
Pharmacol. Rev.,
March 1, 1999;
51(1):
7 - 62.
[Abstract]
[Full Text]
[PDF]
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W. Danysz and C. G. Parsons
Glycine and N-Methyl-D-Aspartate Receptors: Physiological Significance and Possible Therapeutic Applications
Pharmacol. Rev.,
December 1, 1998;
50(4):
597 - 664.
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A. Ivanovic, H. Reilander, B. Laube, and J. Kuhse
Expression and Initial Characterization of a Soluble Glycine Binding Domain of the N-Methyl-D-aspartate Receptor NR1 Subunit
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August 7, 1998;
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L.-H. Jiang, F. Rassendren, A. Surprenant, and R. A. North
Identification of Amino Acid Residues Contributing to the ATP-binding Site of a Purinergic P2X Receptor
J. Biol. Chem.,
October 27, 2000;
275(44):
34190 - 34196.
[Abstract]
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[PDF]
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E. Meddows, B. Le Bourdelles, S. Grimwood, K. Wafford, S. Sandhu, P. Whiting, and R. A. J. McIlhinney
Identification of Molecular Determinants That Are Important in the Assembly of N-Methyl-D-aspartate Receptors
J. Biol. Chem.,
May 25, 2001;
276(22):
18795 - 18803.
[Abstract]
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