I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St. Petersburg, Russia.
Biochemistry. 2011 Sep 27;50(38):8213-20. doi: 10.1021/bi200617v. Epub 2011 Aug 29.
Binding of argiotoxin in the closed state of Ca(2+)-permeable AMPA receptor channels was studied using electrophysiological and molecular modeling approaches. Experimental study unambiguously revealed that argiotoxin is trapped in the closed AMPA receptor channels after agonist dissociation. Docking of the argiotoxin to the channel model based on recently published X-ray structure demonstrated that the drug can be effectively accommodated in the cavity of the closed channel only if the terminal moiety of the molecule penetrates in the narrow portion of the pore below the selectivity filter. Combining these results, we conclude that the selectivity filter of the AMPA receptor channels is not sterically occluded in the closed state.
使用电生理学和分子建模方法研究了 argiotoxin 在 Ca(2+)可渗透 AMPA 受体通道的关闭状态下的结合。实验研究明确揭示,在激动剂解离后,argiotoxin 被捕获在关闭的 AMPA 受体通道中。基于最近发表的 X 射线结构,将 argiotoxin 对接至通道模型表明,只有分子的末端部分穿透位于选择性过滤器下方的孔的狭窄部分,该药物才能有效地容纳在封闭通道的腔中。结合这些结果,我们得出结论,AMPAR 通道的选择性过滤器在关闭状态下没有被空间位阻。