Department of Pharmacological and Physiological Science, and The Center for Excellence in Neuroscience, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Proc Natl Acad Sci U S A. 2011 Aug 16;108(33):13800-5. doi: 10.1073/pnas.1017550108. Epub 2011 Aug 1.
P2X receptors are trimeric cation channels with widespread roles in health and disease. The recent crystal structure of a P2X4 receptor provides a 3D view of their topology and architecture. A key unresolved issue is how ions gain access to the pore, because the structure reveals two different pathways within the extracellular domain. One of these is the central pathway spanning the entire length of the extracellular domain and covering a distance of ≈70 Å. The second consists of three lateral portals, adjacent to the membrane and connected to the transmembrane pore by short tunnels. Here, we demonstrate the preferential use of the lateral portals. Owing to their favorable diameters and equivalent spacing, the lateral portals split the task of ion supply threefold and minimize an ion's diffusive path before it succumbs to transmembrane electrochemical gradients.
P2X 受体是三聚体阳离子通道,在健康和疾病中具有广泛的作用。最近 P2X4 受体的晶体结构提供了它们拓扑结构和架构的 3D 视图。一个未解决的关键问题是离子如何进入孔道,因为该结构揭示了细胞外域内的两条不同途径。其中之一是贯穿细胞外域全长并覆盖约 70Å 的中央途径。另一个由三个侧门组成,它们紧邻膜并通过短隧道与跨膜孔连接。在这里,我们证明了侧门的优先使用。由于它们的有利直径和等效间距,侧门将离子供应的任务分成三份,并在离子屈服于跨膜电化学梯度之前最小化离子的扩散路径。