On the mechanism of calcium permeability and magnesium block in NMDA receptors - a central molecular paradigm in neuroplasticity

关于NMDA受体中钙离子通透性和镁离子阻滞的机制——神经可塑性的核心分子范式

阅读:3

Abstract

Neuroplasticity is a fundamental cellular mechanism underlying learning and memory formation and is primed by the coincidental detection of neurotransmitter release from the presynapse and the subsequent calcium influx upon voltage change in the postsynaptic membrane (Bliss and Collingridge, 1993). Molecular assemblies that achieve these events are N-methyl-D-aspartate receptors (NMDARs), which bind the neurotransmitter glutamate and a co-agonist, either glycine or D-serine, and allow Ca(2+) influx upon relief of the Mg(2+) channel blockade by membrane depolarization. However, the molecular basis governing Ca(2+) permeability and Mg(2+) blockade in NMDAR remains limited. Here, we demonstrate that Ca(2+) permea on through the narrow constriction of the cation selectivity filter involves partial dehydration, as evidenced by multiple Ca(2+) binding sites captured using single-particle cryo-electron microscopy (cryo-EM). In contrast, Mg(2+) binds outside of the selectivity filter through the water network by remaining hydrated, thereby serving as a channel blocker. Furthermore, we show that the lipid network around the selectivity filter influences the stability of Mg(2+) binding. Our study details the critical transmembrane chemistry of NMDAR for initiating neuroplasticity.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。