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-Structure paper
タイトル | Structural basis of kainate subtype glutamate receptor desensitization. |
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ジャーナル・号・ページ | Nature, Vol. 537, Issue 7621, Page 567-571, Year 2016 |
掲載日 | 2016年9月22日 |
![]() | Joel R Meyerson / Sagar Chittori / Alan Merk / Prashant Rao / Tae Hee Han / Mihaela Serpe / Mark L Mayer / Sriram Subramaniam / ![]() |
PubMed 要旨 | Glutamate receptors are ligand-gated tetrameric ion channels that mediate synaptic transmission in the central nervous system. They are instrumental in vertebrate cognition and their dysfunction ...Glutamate receptors are ligand-gated tetrameric ion channels that mediate synaptic transmission in the central nervous system. They are instrumental in vertebrate cognition and their dysfunction underlies diverse diseases. In both the resting and desensitized states of AMPA and kainate receptor subtypes, the ion channels are closed, whereas the ligand-binding domains, which are physically coupled to the channels, adopt markedly different conformations. Without an atomic model for the desensitized state, it is not possible to address a central problem in receptor gating: how the resting and desensitized receptor states both display closed ion channels, although they have major differences in the quaternary structure of the ligand-binding domain. Here, by determining the structure of the kainate receptor GluK2 subtype in its desensitized state by cryo-electron microscopy (cryo-EM) at 3.8 Å resolution, we show that desensitization is characterized by the establishment of a ring-like structure in the ligand-binding domain layer of the receptor. Formation of this 'desensitization ring' is mediated by staggered helix contacts between adjacent subunits, which leads to a pseudo-four-fold symmetric arrangement of the ligand-binding domains, illustrating subtle changes in symmetry that are important for the gating mechanism. Disruption of the desensitization ring is probably the key switch that enables restoration of the receptor to its resting state, thereby completing the gating cycle. |
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手法 | EM (単粒子) / X線回折 |
解像度 | 1.271 - 11.6 Å |
構造データ | ![]() PDB-5cmk: ![]() PDB-5cmm: |
化合物 | ![]() ChemComp-GLU: ![]() ChemComp-LI: ![]() ChemComp-CL: ![]() ChemComp-LY5: ![]() ChemComp-SO4: ![]() ChemComp-HOH: ![]() ChemComp-SYM: |
由来 |
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![]() | TRANSPORT PROTEIN / Membrane protein / SIGNALING PROTEIN / GluK2EM with 2S / 4R-4-methylglutamate / GluK2EM with LY466195 |