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钠离子/氯离子神经递质转运体家族。

The family of Na+/Cl- neurotransmitter transporters.

作者信息

Nelson N

机构信息

Department of Biochemistry, Tel Aviv University, Israel.

出版信息

J Neurochem. 1998 Nov;71(5):1785-803. doi: 10.1046/j.1471-4159.1998.71051785.x.

Abstract

The termination of neurotransmission is achieved by rapid uptake of the released neurotransmitter by specific high-affinity neurotransmitter transporters. Most of these transporters are encoded by a family of genes (Na+/Cl- transporters) having a similar membrane topography of 12 transmembrane helices. An evolutionary tree revealed five distinct subfamilies: gamma-aminobutyric acid transporters, monoamine transporters, amino acid transporters, "orphan" transporters, and the recently discovered bacterial transporters. The bacterial transporters that belong to this family may help to develop heterologous expression systems with the aim of solving the three-dimensional structure of these membrane proteins. Some of the neurotransmitter transporters have been implicated as important sites for drug action. Monoamine transporters, for example, are targeted by major classes of antidepressants, psychostimulants, and antihypertensive drugs. Localization of individual transporters in specific cells and brain areas is pertinent to understanding their contribution to neurotransmission and their potential as targets for drugs. The most important questions in the field include resolving the mechanism of neurotransmitter transport, the structure of the transporters, and the interaction of each transporter in complex neurological activities.

摘要

神经传递的终止是通过特定的高亲和力神经递质转运体快速摄取释放的神经递质来实现的。这些转运体大多由一个基因家族(钠/氯转运体)编码,该家族具有相似的12个跨膜螺旋的膜拓扑结构。进化树显示有五个不同的亚家族:γ-氨基丁酸转运体、单胺转运体、氨基酸转运体、“孤儿”转运体以及最近发现的细菌转运体。属于这个家族的细菌转运体可能有助于开发异源表达系统,以解决这些膜蛋白的三维结构问题。一些神经递质转运体已被认为是药物作用的重要位点。例如,单胺转运体是主要类型的抗抑郁药、精神兴奋剂和抗高血压药物的作用靶点。单个转运体在特定细胞和脑区的定位对于理解它们对神经传递的贡献以及它们作为药物靶点的潜力至关重要。该领域最重要的问题包括解析神经递质转运机制、转运体结构以及每个转运体在复杂神经活动中的相互作用。

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