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通过N-糖基化揭示的两种海人酸受体亚基的跨膜拓扑结构

Transmembrane topology of two kainate receptor subunits revealed by N-glycosylation.

作者信息

Wo Z G, Oswald R E

机构信息

Department of Pharmacology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.

出版信息

Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7154-8. doi: 10.1073/pnas.91.15.7154.

Abstract

Glutamate receptors are the primary excitatory neurotransmitter receptors in vertebrate brain and are of critical importance to a wide variety of neurological processes. Recent reports suggest that ionotropic glutamate receptors may have a unique transmembrane topology not shared by other ligand-gated ion channels. We report here the cloning of cDNAs from goldfish brain encoding two homologous kainate receptors with protein molecular masses of 41 kDa. Using a cell-free translation/translocation system, we show that (i) a portion of these receptors previously thought to be a large intracellular loop is actually located extracellularly and (ii) the putative second transmembrane region of the receptor thought to line the ion channel may not be a true membrane-spanning domain. An alternative model for the transmembrane topology of kainate receptors is proposed that could potentially serve as a framework for future detailed study of the structure of this important class of neurotransmitter receptors.

摘要

谷氨酸受体是脊椎动物大脑中的主要兴奋性神经递质受体,对多种神经过程至关重要。最近的报道表明,离子型谷氨酸受体可能具有一种独特的跨膜拓扑结构,这是其他配体门控离子通道所没有的。我们在此报告从金鱼脑中克隆出编码两种同源红藻氨酸受体的cDNA,其蛋白质分子量为41 kDa。使用无细胞翻译/转位系统,我们发现:(i)这些受体中先前被认为是一个大的细胞内环的部分实际上位于细胞外;(ii)被认为构成离子通道的受体假定的第二个跨膜区域可能不是一个真正的跨膜结构域。我们提出了一种红藻氨酸受体跨膜拓扑结构的替代模型,该模型可能为今后详细研究这类重要神经递质受体的结构提供一个框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/beba/44357/be8f9ac1ec68/pnas01137-0450-a.jpg

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