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The Journal of Neuroscience, January 15, 2001, 21(2):392-400
Three Pairs of Cysteine Residues Mediate Both Redox and
Zn2+ Modulation of the NMDA Receptor
Yun-Beom
Choi1, 2,
Huei-Sheng Vincent
Chen1, 2, and
Stuart A.
Lipton1, 2
1 Center for Neuroscience and Aging, The Burnham
Institute, La Jolla, California 92037, and
2 Cerebrovascular and NeuroScience Research Institute,
Brigham and Women's Hospital, Program in Neuroscience, Harvard Medical
School, Boston, Massachusetts 02115
NMDA receptor activity is modulated by various compounds, including
sulfhydryl redox agents and Zn2+. In addition to a
slow and persistent component of redox modulation common to all NMDA
receptors, NR1/NR2A receptors uniquely have a rapid and reversible
component that has been variously attributed to redox or
Zn2+ effects. Here we show that this rapid
modulatory effect can be described by two time constants with
relatively fast (~6 sec) and intermediate (60 sec) half lives, and it
is likely to be attributable to both redox agents and
Zn2+. Using site-directed mutagenesis, we identified
three pairs of cysteine residues that underlie the various kinetic
components of redox modulation of NMDA-evoked currents in
Xenopus oocytes expressing NR1/NR2A receptors: (1) Cys
87 and Cys 320 in NR2A underlie the fast component, (2) Cys 79 and Cys 308 in NR1 underlie the intermediate component, and (3) Cys 744 and Cys 798 in NR1 underlie the persistent component. Mutation of these
redox-sensitive cysteine residues also affects high-affinity,
voltage-independent Zn2+ inhibition that is specific
to NR1/NR2A receptors. Exposure to methanethiosulfonate agents that
modify cysteine residues did not block the Zn2+
inhibition. Thus, these cysteine residues do not appear to coordinate Zn2+ directly. Instead, the redox status of these
cysteine residues may modulate the sensitivity of the receptor
to Zn2+.
Key words:
NMDA receptor; glutamate; zinc; redox; recombinant cDNA; cysteine; dithiothreitol
Copyright © 2001 Society for Neuroscience 0270-6474/01/212392-09$05.00/0
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