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dc.contributor.authorChen, Xiaobing
dc.contributor.authorNelson, Christopher D.
dc.contributor.authorLi, Xiang
dc.contributor.authorWinters, Christine A.
dc.contributor.authorAzzam, Rita
dc.contributor.authorSousa, Alioscka A.
dc.contributor.authorLeapman, Richard D.
dc.contributor.authorGainer, Harold
dc.contributor.authorSheng, Morgan Hwa-Tze
dc.contributor.authorReese, Thomas S.
dc.date.accessioned2011-11-09T16:01:08Z
dc.date.available2011-11-09T16:01:08Z
dc.date.issued2011-03
dc.date.submitted2011-03
dc.identifier.issn0270-6474
dc.identifier.issn1529-2401
dc.identifier.urihttp://hdl.handle.net/1721.1/66976
dc.description.abstractPSD-95, a membrane-associated guanylate kinase, is the major scaffolding protein in the excitatory postsynaptic density (PSD) and a potent regulator of synaptic strength. Here we show that PSD-95 is in an extended configuration and positioned into regular arrays of vertical filaments that contact both glutamate receptors and orthogonal horizontal elements layered deep inside the PSD in rat hippocampal spine synapses. RNA interference knockdown of PSD-95 leads to loss of entire patches of PSD material, and electron microscopy tomography shows that the patchy loss correlates with loss of PSD-95-containing vertical filaments, horizontal elements associated with the vertical filaments, and putative AMPA receptor-type, but not NMDA receptor-type, structures. These observations show that the orthogonal molecular scaffold constructed from PSD-95-containing vertical filaments and their associated horizontal elements is essential for sustaining the three-dimensional molecular organization of the PSD. Our findings provide a structural basis for understanding the functional role of PSD-95 at the PSD.en_US
dc.description.sponsorshipNational Institute of Neurological Disorders and Stroke (U.S.)en_US
dc.description.sponsorshipNational Institute of Biomedical Imaging and Bioengineering (U.S.)en_US
dc.description.sponsorshipHoward Hughes Medical Instituteen_US
dc.language.isoen_US
dc.publisherSociety for Neuroscienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1523/jneurosci.5968-10.2011en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSFNen_US
dc.titlePSD-95 Is Required to Sustain the Molecular Organization of the Postsynaptic Densityen_US
dc.typeArticleen_US
dc.identifier.citationChen, X. et al. “PSD-95 Is Required to Sustain the Molecular Organization of the Postsynaptic Density.” Journal of Neuroscience 31 (2011): 6329-6338.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentPicower Institute for Learning and Memoryen_US
dc.contributor.approverSheng, Morgan Hwa-Tze
dc.contributor.mitauthorNelson, Christopher D.
dc.contributor.mitauthorSheng, Morgan Hwa-Tze
dc.relation.journalJournal of Neuroscienceen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsChen, X.; Nelson, C. D.; Li, X.; Winters, C. A.; Azzam, R.; Sousa, A. A.; Leapman, R. D.; Gainer, H.; Sheng, M.; Reese, T. S.en
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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