2ojt
From Proteopedia
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'''Structure and mechanism of kainate receptor modulation by anions''' | '''Structure and mechanism of kainate receptor modulation by anions''' | ||
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[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Mayer, M L.]] | [[Category: Mayer, M L.]] | ||
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Revision as of 08:03, 4 May 2008
Structure and mechanism of kainate receptor modulation by anions
Overview
L-glutamate, the major excitatory neurotransmitter in the human brain, activates a family of ligand-gated ion channels, the major subtypes of which are named AMPA, kainate, and NMDA receptors. In common with many signal transduction proteins, glutamate receptors are modulated by ions and small molecules, including Ca(2+), Mg(2+), Zn(2+), protons, polyamines, and steroids. Strikingly, the activation of kainate receptors by glutamate requires the presence of both Na(+) and Cl(-) in the extracellular solution, and in the absence of these ions, receptor activity is abolished. Here, we identify the site and mechanism of action of anions. Surprisingly, we find that Cl(-) ions are essential structural components of kainate receptors. Cl(-) ions bind in a cavity formed at the interface between subunits in a dimer pair. In the absence of Cl(-), dimer stability is reduced, the rate of desensitization increases, and the fraction of receptors competent for activation by glutamate drops precipitously.
About this Structure
2OJT is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.
Reference
Structure and mechanism of kainate receptor modulation by anions., Plested AJ, Mayer ML, Neuron. 2007 Mar 15;53(6):829-41. PMID:17359918 Page seeded by OCA on Sun May 4 11:03:34 2008