Single-channel analysis of an NMDA receptor possessing a mutation in the region of the glutamate binding site

Authors

  • Lesley C. Anson,

    1. Department of Pharmacology and Wellcome Laboratory for Molecular Pharmacology, University College London, Gower Street, London WC1E 6BT, UK
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  • Ralf Schoepfer,

    1. Department of Pharmacology and Wellcome Laboratory for Molecular Pharmacology, University College London, Gower Street, London WC1E 6BT, UK
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  • David Colquhoun,

    1. Department of Pharmacology and Wellcome Laboratory for Molecular Pharmacology, University College London, Gower Street, London WC1E 6BT, UK
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  • David J. A. Wyllie

    Corresponding author
    1. Department of Pharmacology and Wellcome Laboratory for Molecular Pharmacology, University College London, Gower Street, London WC1E 6BT, UK
    • Corresponding author's present address
      D. J. A. Wyllie: Department of Neuroscience, University of Edinburgh, 1 George Square, Edinburgh EH8 9JZ, UK. Email: david.j.a.wyllie@ed.ac.uk

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  • Author's present address L. C. Anson: Nature Editorial Office, Macmillan Magazines Ltd, Porters South, 4–6 Crinan Street, London N1 9XW, UK.

Abstract

  • 1Recombinant NR1a/NR2A(T671A) N-methyl-D-aspartate (NMDA) receptor-channels, which carry a point mutation in the putative glutamate binding site that reduces glutamate potency by around 1000-fold, have been expressed in Xenopus laevis oocytes and their single-channel properties examined using patch-clamp recording techniques.
  • 2Shut time distributions of channel activity were fitted with a mixture of five exponential components. The first three components in each distribution were considered to occur within a channel activation as they exhibited little or no dependence on agonist concentration.
  • 3Bursts of single-channel openings were defined by a critical gap length with a mean of 5.65 ± 0.37 ms. Shut intervals with a duration longer than this value were considered to occur between separate bursts of channel openings. Distributions of the lengths of bursts of openings were fitted with a mixture of four exponential components. The longest two components carried the majority of the charge transfer in the channel recordings and had means of 7.71 ± 1.1 and 37.7 ± 4.3 ms. The overall probability of a channel being open during a burst was high (mean 0.92 ± 0.01).
  • 4Brief concentration jumps (1 ms) of 10 mm glutamate were applied to outside-out patches so that a comparison between the macroscopic current relaxation and steady-state single-channel activity evoked by glutamate could be made. The decay of such macroscopic currents was fitted with a single exponential component with a mean of 32.0 ± 3.53 ms.
  • 5The good agreement between macroscopic current decay following brief agonist exposure and the value for the slowest component of the burst length distribution suggests that the bursts of openings that we identified in steady-state recordings represent individual activations of recombinant NR1a/NR2A(T671A) NMDA receptor-channels.
  • 6A new way of displaying geometric distributions is suggested, and the utility of a modified definition of the ‘probability of being open within a burst’ is discussed.
  • 7The single-channel data that we present in this paper support further the idea that the point mutation T671A in the NR2A NMDA receptor subunit affects mainly the ability of glutamate to remain bound to these channels.

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