Transmembrane topology of two kainate receptor subunits revealed by N-glycosylation.
Author(s) -
Z. Galen Wo,
Robert E. Oswald
Publication year - 1994
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.91.15.7154
Subject(s) - kainate receptor , rhodopsin like receptors , class c gpcr , ionotropic effect , neurotransmitter receptor , biology , microbiology and biotechnology , transmembrane domain , ion channel , receptor , ligand gated ion channel , transmembrane protein , ion channel linked receptors , glutamate receptor , neuroscience , metabotropic receptor , metabotropic glutamate receptor , biochemistry , ampa receptor
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.
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