Poulsen Mette H, Andersen Jacob, Christensen Rune, Hansen Kasper B, Traynelis Stephen F, Strømgaard Kristian, Kristensen Anders Skov
Department of Drug Design and Pharmacology, University of Copenhagen, 2100 København, Denmark.
Department of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA.
J Mol Biol. 2015 Jan 16;427(1):176-89. doi: 10.1016/j.jmb.2014.05.017. Epub 2014 May 24.
The N-methyl-d-aspartate receptors (NMDARs) constitute an important class of ligand-gated cation channels that are involved in the majority of excitatory neurotransmission in the human brain. Compounds that bind in the NMDAR ion channel and act as blockers are use- and voltage-dependent inhibitors of NMDAR activity and have therapeutic potential for treatment of a variety of brain diseases or as pharmacological tools for studies of the neurobiological role of NMDARs. We have performed a kinetic analysis of the blocking mechanism of the prototypical polyamine toxin NMDAR ion channel blocker argiotoxin-636 (ArgTX-636) at recombinant GluN1/2A receptors to provide detailed information on the mechanism of block. The predicted binding site of ArgTX-636 is in the pore region of the NMDAR ion channel formed by residues in the transmembrane M3 and the M2 pore-loop segments of the GluN1 and GluN2A subunits. To assess the predicted binding mode in further detail, we performed an alanine- and glycine-scanning mutational analysis of this pore-loop segment to systematically probe the role of pore-lining M2 residues in GluN1 and GluN2A in the channel block by ArgTX-636. Comparison of M2 positions in GluN1 and GluN2A where mutation influences ArgTX-636 potency suggests differential contribution of the M2-loops of GluN1 and GluN2A to binding of ArgTX-636. The results of the mutational analysis are highly relevant for the future structure-based development of argiotoxin-derived NMDAR channel blockers.
N-甲基-D-天冬氨酸受体(NMDARs)构成了一类重要的配体门控阳离子通道,参与了人类大脑中大部分兴奋性神经传递。结合于NMDAR离子通道并作为阻滞剂起作用的化合物是NMDAR活性的使用和电压依赖性抑制剂,对治疗多种脑部疾病具有治疗潜力,或作为研究NMDARs神经生物学作用的药理学工具。我们对典型的多胺毒素NMDAR离子通道阻滞剂精毒素-636(ArgTX-636)在重组GluN1/2A受体上的阻断机制进行了动力学分析,以提供有关阻断机制的详细信息。ArgTX-636的预测结合位点位于由GluN1和GluN2A亚基的跨膜M3和M2孔环段中的残基形成的NMDAR离子通道的孔区域。为了更详细地评估预测的结合模式,我们对该孔环段进行了丙氨酸和甘氨酸扫描突变分析,以系统地探究GluN1和GluN2A中孔内衬M2残基在ArgTX-636对通道的阻断作用中的作用。比较GluN1和GluN2A中突变影响ArgTX-636效力的M2位置,表明GluN1和GluN2A的M2环对ArgTX-636结合的贡献不同。突变分析的结果对于未来基于结构开发精毒素衍生的NMDAR通道阻滞剂具有高度相关性。