Tikhonov Denis B
Sechenov Institute of Evolutionary Physiology and Biochemistry RAS, St. Petersburg, Russia.
Mol Membr Biol. 2007 Mar-Apr;24(2):135-47. doi: 10.1080/09687860601008806.
Ionotropic glutamate receptors belong to the superfamily of P-loop channels as well as K(+), Na(+), and Ca(2+) channels. However, the structural similarity between ion channels of the glutamate receptors and K(+) channels is a matter of discussion. The aim of this study was to analyze differences between the structures of K(+) channels and glutamate receptor channels. For this purpose, homology models of NMDA and AMPA receptor channels (M2 and M3 segments) were built using X-ray structures of K(+) channels as templates. The models were optimized and used to reproduce specific data on the structure of glutamate receptor channels. Particular attention was paid to the data of the binding of channel blockers and to the results of scanning mutagenesis. The modeling demonstrates that properties of glutamate receptor channel can be reproduced assuming only local structural deformations of the K(+) channel templates. The most valuable differences were found in the selectivity-filter region, whereas helical parts of M2 and M3 segments could have similar spatial organization with homologous segments in K(+) channels. It is concluded that the current experimental data on glutamate receptor channels does not reveal global structural differences with K(+) channels.
离子型谷氨酸受体属于P环通道超家族,以及钾离子、钠离子和钙离子通道。然而,谷氨酸受体的离子通道与钾离子通道之间的结构相似性仍存在争议。本研究的目的是分析钾离子通道与谷氨酸受体通道结构之间的差异。为此,以钾离子通道的X射线结构为模板,构建了NMDA和AMPA受体通道(M2和M3片段)的同源模型。对模型进行了优化,并用于重现谷氨酸受体通道结构的特定数据。特别关注了通道阻滞剂结合的数据以及扫描诱变的结果。建模表明,仅假设钾离子通道模板存在局部结构变形,就可以重现谷氨酸受体通道的特性。在选择性过滤器区域发现了最有价值的差异,而M2和M3片段的螺旋部分可能与钾离子通道中的同源片段具有相似的空间组织。得出的结论是,目前关于谷氨酸受体通道的实验数据并未揭示其与钾离子通道的整体结构差异。