Tikhonov D B
I. M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, 44 M. Torez Prospekt, St. Petersburg, Russia.
Neurosci Behav Physiol. 2008 Jun;38(5):461-9. doi: 10.1007/s11055-008-9003-8. Epub 2008 Jul 18.
Potential-dependent sodium channels play a leading role in generating action potentials in excitable cells. Sodium channels are the site of action of a variety of modulator ligands. Despite numerous studies, the mechanisms of action of many modulators remain incompletely understood. The main reason that many important questions cannot be resolved is that there is a lack of precise data on the structures of the channels themselves. Structurally, potential-dependent sodium channels are members of the P-loop channel superfamily, which also include potassium and calcium channels and glutamate receptor channels. Crystallization of a series of potassium channels showed that it was possible to analyze the structures of different members of the superfamily using the "homologous modeling" method. The present study addresses model investigations of the actions of ligands of sodium channels, including tetrodotoxin and batrachotoxin, as well as local anesthetics. Comparison of experimental data on sodium channel ligands with x-ray analysis data allowed us to reach a new level of understanding of the mechanisms of channel modulation and to propose a series of experimentally verifiable hypotheses.
电压依赖性钠通道在可兴奋细胞动作电位的产生中起主导作用。钠通道是多种调节性配体的作用位点。尽管进行了大量研究,但许多调节剂的作用机制仍未完全明了。许多重要问题无法解决的主要原因是缺乏关于通道自身结构的确切数据。从结构上看,电压依赖性钠通道是P环通道超家族的成员,该超家族还包括钾通道、钙通道和谷氨酸受体通道。一系列钾通道的结晶表明,使用“同源建模”方法可以分析超家族不同成员的结构。本研究涉及钠通道配体作用的模型研究,包括河豚毒素、蟾毒素以及局部麻醉药。将钠通道配体的实验数据与X射线分析数据进行比较,使我们对通道调节机制的理解达到了一个新水平,并提出了一系列可通过实验验证的假设。