Popescu Gabriela, Auerbach Anthony
Center for Single Molecule Biophysics and the Department of Physiology and Biophysics, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York 14214, USA.
Nat Neurosci. 2003 May;6(5):476-83. doi: 10.1038/nn1044.
N-methyl-D-aspartate receptor (NMDAR) channels mediate the slow component of excitatory potentials at glutamatergic synapses. They have complex kinetic behavior, and much remains to be understood about NMDAR gating mechanisms and the molecular events that shape the synaptic current. Here we show that an individual NMDAR produces at least three stable patterns of activity. For all modes, channels gate by the same mechanism and can occupy either of two open states. The relative stability of the open states differs across modes because of a common perturbation to the NMDAR structure that may be subject to cellular control. Simulations indicate that native NMDAR-mediated synaptic responses arise mainly from the most common mode, and that the slow rise and decay of the current can be attributed to multiple transitions between fully liganded open and closed states rather than to agonist dissociation.
N-甲基-D-天冬氨酸受体(NMDAR)通道介导谷氨酸能突触处兴奋性电位的慢成分。它们具有复杂的动力学行为,关于NMDAR门控机制以及形成突触电流的分子事件仍有许多有待了解之处。在这里,我们表明单个NMDAR产生至少三种稳定的活动模式。对于所有模式,通道通过相同的机制门控,并且可以占据两种开放状态中的任何一种。由于对NMDAR结构的共同扰动(可能受细胞控制),开放状态的相对稳定性在不同模式之间有所不同。模拟表明,天然NMDAR介导的突触反应主要源于最常见的模式,并且电流的缓慢上升和衰减可归因于完全配体化的开放和关闭状态之间的多次转换,而不是激动剂解离。