1,666 research outputs found
Chimeric glutamate receptor subunits reveal the transmembrane domain is sufficient for NMDA receptor pore properties but some positive allosteric modulators require additional domains
NMDA receptors are ligand-gated ion channels that underlie transmission at excitatory synapses and play an important role in regulating synaptic strength and stability. Functional NMDA receptors require two copies of the GluN1 subunit coassembled with GluN2 (and/or GluN3) subunits into a heteromeric tetramer. A diverse array of allosteric modulators can upregulate or downregulate NMDA receptor activity. These modulators include both synthetic compounds and endogenous modulators, such as cis-unsaturated fatty acids, 24(S)-hydroxycholesterol, and various neurosteroids. To evaluate the structural requirements for the formation and allosteric modulation of NMDA receptor pores, we have replaced portions of the rat GluN1, GluN2A, and GluN2B subunits with homologous segments from the rat GluK2 kainate receptor subunit. Our results with these chimeric constructs show that the NMDA receptor transmembrane domain is sufficient to account for most pore properties, but that regulation by some allosteric modulators requires additional cytoplasmic or extracellular domains. SIGNIFICANCE STATEMENT Glutamate receptors mediate excitatory synaptic transmission by forming cation channels through the membrane that open upon glutamate binding. Although many compounds have been identified that regulate glutamate receptor activity, in most cases the detailed mechanisms that underlie modulation are poorly understood. To identify what parts of the receptor are essential for pore formation and sensitivity to allosteric modulators, we generated chimeric subunits that combined segments from NMDA and kainate receptors, subtypes with distinct pharmacological profiles. Surprisingly, our results identify separate domain requirements for allosteric potentiation of NMDA receptor pores by pregnenolone sulfate, 24(S)-hydroxycholesterol, and docosahexaenoic acid, three endogenous modulators derived from membrane constituents. Understanding where and how these compounds act on NMDA receptors should aid in designing better therapeutic agents
Cadmium activates AMPA and NMDA receptors with M3 helix cysteine substitutions
AMPA and NMDA receptors are ligand-gated ion channels that depolarize postsynaptic neurons when activated by the neurotransmitter L-glutamate. Changes in the distribution and activity of these receptors underlie learning and memory, but excessive change is associated with an array of neurological disorders, including cognitive impairment, developmental delay, and epilepsy. All of the ionotropic glutamate receptors (iGluRs) exhibit similar tetrameric architecture, transmembrane topology, and basic framework for activation; conformational changes induced by extracellular agonist binding deform and splay open the inner helix bundle crossing that occludes ion flux through the channel. NMDA receptors require agonist binding to all four subunits, whereas AMPA and closely related kainate receptors can open with less than complete occupancy. In addition to conventional activation by agonist binding, we recently identified two locations along the inner helix of the GluK2 kainate receptor subunit where cysteine (Cys) substitution yields channels that are opened by exposure to cadmium ions, independent of agonist site occupancy. Here, we generate AMPA and NMDA receptor subunits with homologous Cys substitutions and demonstrate similar activation of the mutant receptors by Cd. Coexpression of the auxiliary subunit stargazin enhanced Cd potency for activation of Cys-substituted GluA1 and altered occlusion upon treatment with sulfhydryl-reactive MTS reagents. Mutant NMDA receptors displayed voltage-dependent Mg block of currents activated by agonist and/or Cd as well as asymmetry between Cd effects on Cys-substituted GluN1 versus GluN2 subunits. In addition, Cd activation of each Cys-substituted iGluR was inhibited by protons. These results, together with our earlier work on GluK2, reveal a novel mechanism shared among the three different iGluR subtypes for prying open the gate that controls ion entry into the pore
Coexistence Curve Singularities at Critical End Points
We report an extensive Monte Carlo study of critical end point behaviour in a
symmetrical binary fluid mixture. On the basis of general scaling arguments,
singular behaviour is predicted in the diameter of the liquid-gas coexistence
curve as the critical end point is approached. The simulation results show
clear evidence for this singularity, as well as confirming a previously
predicted singularity in the coexistence chemical potential. Both singularities
should be detectable experimentally.Comment: 9 pages Revtex, 3 figures. To appear in Phys. Rev. Let
Wetting of a symmetrical binary fluid mixture on a wall
We study the wetting behaviour of a symmetrical binary fluid below the
demixing temperature at a non-selective attractive wall. Although it demixes in
the bulk, a sufficiently thin liquid film remains mixed. On approaching
liquid/vapour coexistence, however, the thickness of the liquid film increases
and it may demix and then wet the substrate. We show that the wetting
properties are determined by an interplay of the two length scales related to
the density and the composition fluctuations. The problem is analysed within
the framework of a generic two component Ginzburg-Landau functional
(appropriate for systems with short-ranged interactions). This functional is
minimized both numerically and analytically within a piecewise parabolic
potential approximation. A number of novel surface transitions are found,
including first order demixing and prewetting, continuous demixing, a
tricritical point connecting the two regimes, or a critical end point beyond
which the prewetting line separates a strongly and a weakly demixed film. Our
results are supported by detailed Monte Carlo simulations of a symmetrical
binary Lennard-Jones fluid at an attractive wall.Comment: submitted to Phys. Rev.
Separating content-specific retrieval from post-retrieval processing
According to cortical reinstatement accounts, neural processes engaged at the time of encoding are re-engaged at the time of memory retrieval. The temporal precision of event-related potentials (ERPs) has been exploited to assess this possibility, and in this study ERPs were acquired while people made memory judgments to visually presented words encoded in two different ways. There were reliable differences between the scalp distributions of the signatures of successful retrieval of different contents from 300 to 1100 ms after stimulus presentation. Moreover, the scalp distributions of these content-sensitive effects changed during this period. These findings are, to our knowledge, the first demonstration in one study that ERPs reflect content-specific processing in two separable ways: first, via reinstatement, and second, via downstream processes that operate on recovered information in the service of memory judgments
The Lennard-Jones-Devonshire cell model revisited
We reanalyse the cell theory of Lennard-Jones and Devonshire and find that in
addition to the critical point originally reported for the 12-6 potential (and
widely quoted in standard textbooks), the model exhibits a further critical
point. We show that the latter is actually a more appropriate candidate for
liquid-gas criticality than the original critical point.Comment: 5 pages, 3 figures, submitted to Mol. Phy
Direct real-time neural evidence for task-set inertia
One influential explanation for the costs incurred when switching between tasks is that they reflect interference arising from completing the previous task—known as task set inertia. We report a novel approach for assessing task-set inertia in a memory experiment using event related potentials (ERPs). After a study phase participants completed a test block in which they switched between a memory task (retrieving information from the study phase) and a perceptual task. These tasks alternated every two trials. An ERP index of the retrieval of study information was evident in the memory task. It was also present on the first trial of the perceptual task but was markedly attenuated on the second. Moreover, this task-irrelevant ERP activity was positively correlated with a behavioral cost associated with switching between tasks. This real-time measure of neural activity thus provides direct evidence of task-set inertia, its duration, and the functional role it plays in switch costs
Radial symmetry in a chimeric glutamate receptor pore
Ionotropic glutamate receptors comprise two conformationally different A/C and B/D subunit pairs. Closed channels exhibit 4-fold radial symmetry in the transmembrane domain (TMD) but transition to 2-fold dimer-of-dimers symmetry for extracellular ligand binding and N-terminal domains. Here, to evaluate symmetry in open pores we analyzed interaction between the Q/R editing site near the pore loop apex and the transmembrane M3 helix of kainate receptor subunit GluK2. Chimaeric subunits that combined the GluK2 TMD with extracellular segments from NMDA receptors, which are obligate heteromers, yielded channels made up of A/C and B/D subunit pairs with distinct substitutions along M3 and/or Q/R site editing status, in an otherwise identical homotetrameric TMD. Our results indicate that Q/R site interaction with M3 occurs within individual subunits and is essentially the same for both A/C and B/D subunit conformations, suggesting that 4-fold pore symmetry persists in the open state
Continuous demixing at liquid-vapor coexistence in a symmetrical binary fluid mixture
We report a Monte Carlo finite-size scaling study of the demixing transition
of a symmetrical Lennard-Jones binary fluid mixture. For equal concentration of
species, and for a choice of the unlike-to-like interaction ratio delta=0.7,
this transition is found to be continuous at liquid-vapor coexistence. The
associated critical end point exhibits Ising-like universality. These findings
confirm those of earlier smaller scale simulation studies of the same model,
but contradict the findings of recent integral equation and hierarchical
reference theory investigations.Comment: 7 pages, 6 figure
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