Publications by authors named "Jue Xiang Wang"

Article Synopsis
  • Current research has developed specific compounds for some NMDAR subtypes (GluN2A and GluN2B), but options for GluN2C and GluN2D are limited and not very effective.
  • The study identified UBP791 as a selective inhibitor for GluN2C/2D receptors and provided insights into its binding mechanism, leading to the creation of UBP1700, which is more potent and selective for these subtypes.
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N-Methyl-d-aspartate receptors (NMDARs) are glutamate-gated ion channels, which are critically involved in brain development, learning and memory, cognition, as well as a number of neurological diseases and disorders. Structural biology of NMDARs has been challenging due to technical difficulties associated with assembling a number of different membrane protein subunits. Here, we review historical X-ray crystallographic studies on isolated extracellular domains, which are still the most effective mean to delineate compound binding modes, as well as the most recent studies using electron cryo-microscopy (cryo-EM).

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