Gerstbrein K, Sitte H H
Institute of Pharmacology, Center for Biomolecular Medicine and Pharmacology, Medical University Vienna, Währingerstrasse 13a, 1090 Vienna, Austria.
Handb Exp Pharmacol. 2006(175):95-111. doi: 10.1007/3-540-29784-7_5.
Traditionally, substrate translocation by neurotransmitter transporters has been described by the alternate access model. Recent structural data obtained with three distantly related transporters have also been interpreted as supportive of this model, because conformational correlates were visualized (inward-facing conformation, occluded state). However, the experimental evidence is overwhelmingly in favour of a more complex mode of operation: Transporters also exist in conformations that do not seal the permeation pathway. These conformations support a channel-like activity, including random permeation of substrate and co-substrate ions in a single-file mode. It is likely that the channel-like activity is modified by the interaction of the transporters with accessory proteins and regulatory kinases. Finally, channel-like activity is instrumental to understand the mechanism of action of amphetamines.
传统上,神经递质转运体介导的底物转运是由交替访问模型来描述的。最近通过三种远亲转运体获得的结构数据也被解释为支持该模型,因为观察到了构象相关性(内向构象、堵塞状态)。然而,实验证据压倒性地支持一种更为复杂的运作模式:转运体也存在不封闭渗透途径的构象。这些构象支持一种类似通道的活性,包括底物和共底物离子以单列模式随机渗透。很可能这种类似通道的活性会因转运体与辅助蛋白和调节激酶的相互作用而改变。最后,类似通道的活性有助于理解苯丙胺的作用机制。