Quick M W
Department of Biological Sciences, University of Southern California, HNB 228, 3641 Watt Way, Los Angeles, CA 90089-2520, USA.
Handb Exp Pharmacol. 2006(175):181-96. doi: 10.1007/3-540-29784-7_9.
The SNARE hypothesis of vesicle fusion proposes that a series of protein-protein interactions governs the delivery of vesicles to various membrane targets such as the Golgi network and the plasma membrane. Key players in this process include members of the syntaxin family of membrane proteins. The first member identified in this family, syntaxin 1A, plays an essential role in the docking and fusion of neurotransmitter-containing vesicles to the presynaptic membrane of neurons. Syntaxin 1A and other syntaxin family members have also been shown to interact with, and directly regulate, a variety of ion channels. More recently, the family of plasma membrane neurotransmitter transporters, proteins that function in part to control transmitter levels in brain, have been shown to be direct targets of syntaxin 1A regulation. This regulation involves both the trafficking of transporters as well as the control of ion and transmitter flux through transporters. In this chapter, the functional effects of syntaxin-transporter interactions are reviewed, and how such interactions may regulate neuronal signaling are considered.
囊泡融合的SNARE假说提出,一系列蛋白质-蛋白质相互作用控制着囊泡向各种膜靶点(如高尔基体网络和质膜)的运输。这一过程中的关键参与者包括膜蛋白Syntaxin家族的成员。该家族中第一个被鉴定的成员Syntaxin 1A,在含神经递质的囊泡与神经元突触前膜的对接和融合中起重要作用。Syntaxin 1A和其他Syntaxin家族成员也已被证明与多种离子通道相互作用并直接调节它们。最近,质膜神经递质转运体家族,即部分功能是控制大脑中递质水平的蛋白质,已被证明是Syntaxin 1A调节的直接靶点。这种调节既涉及转运体的运输,也涉及通过转运体对离子和递质通量的控制。在本章中,将综述Syntaxin与转运体相互作用的功能效应,并探讨这种相互作用如何调节神经元信号传导。