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环境因素和亚基组成对 NMDAR 激活效率的调节。

Regulation of NMDAR activation efficiency by environmental factors and subunit composition.

机构信息

Graduate Program in Biochemistry and Structural Biology, Stony Brook University , Stony Brook, NY, USA.

Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY, USA.

出版信息

J Gen Physiol. 2025 Jan 6;157(1). doi: 10.1085/jgp.202413637. Epub 2024 Nov 22.

Abstract

NMDA receptors (NMDAR) convert the major excitatory neurotransmitter glutamate into a synaptic signal. A key question is how efficiently the ion channel opens in response to the rapid exposure to presynaptic glutamate release. Here, we applied glutamate to single channel outside-out patches and measured the successes of channel openings and the latency to first opening to assay the activation efficiency of NMDARs under different physiological conditions and with different human subunit compositions. For GluN1/GluN2A receptors, we find that various factors, including intracellular ATP and GTP, can enhance the efficiency of activation presumably via the intracellular C-terminal domain. Notably, an energy-based internal solution or increasing the time between applications to increase recovery time improved efficiency. However, even under these optimized conditions and with a 1-s glutamate application, there remained around 10-15% inefficiency. Channel activation became more inefficient with brief synaptic-like pulses of glutamate at 2 ms. Of the different NMDAR subunit compositions, GluN2B-containing NMDARs showed the lowest success rate and longest latency to first openings, highlighting that they display the most distinct activation mechanism. In contrast, putative triheteromeric GluN1/GluN2A/GluN2B receptors showed high activation efficiency. Despite the low open probability, NMDARs containing either GluN2C or GluN2D subunits displayed high activation efficiency, nearly comparable with that for GluN2A-containing receptors. These results highlight that activation efficiency in NMDARs can be regulated by environmental surroundings and varies across different subunits.

摘要

N-甲基-D-天冬氨酸受体(NMDAR)将主要的兴奋性神经递质谷氨酸转化为突触信号。一个关键问题是,离子通道在快速暴露于突触前谷氨酸释放时,其开放效率如何。在这里,我们将谷氨酸应用于单通道胞外小片中,并测量通道开放的成功率和首次开放的潜伏期,以检测不同生理条件下和不同人亚基组成的 NMDAR 的激活效率。对于 GluN1/GluN2A 受体,我们发现包括细胞内 ATP 和 GTP 在内的各种因素可以通过细胞内 C 末端结构域增强激活效率。值得注意的是,基于能量的内部溶液或增加应用之间的时间以增加恢复时间可以提高效率。然而,即使在这些优化条件下,并且应用 1 秒的谷氨酸,仍然存在约 10-15%的低效。在 2 毫秒的短暂突触样谷氨酸脉冲下,通道激活变得更加低效。在不同的 NMDAR 亚基组成中,含有 GluN2B 的 NMDAR 显示出最低的成功率和首次开放的最长潜伏期,这突出表明它们显示出最独特的激活机制。相比之下,假定的三杂合 GluN1/GluN2A/GluN2B 受体显示出高的激活效率。尽管开放概率较低,但含有 GluN2C 或 GluN2D 亚基的 NMDAR 显示出高的激活效率,几乎可与含有 GluN2A 的受体相媲美。这些结果强调了 NMDAR 中的激活效率可以通过环境和不同的亚基而变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c01/11586625/00bfcdd72fcd/jgp_202413637_fig1.jpg

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