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dc.contributor.authorHan, Xue
dc.contributor.authorChow, Brian Y.
dc.contributor.authorZhou, Huihui
dc.contributor.authorKlapoetke, Nathan Cao
dc.contributor.authorChuong, Amy S.
dc.contributor.authorRajimehr, Reza
dc.contributor.authorYang, Aimei
dc.contributor.authorBaratta, Michael V.
dc.contributor.authorWinkle, Jonathan Andrew
dc.contributor.authorDesimone, Robert
dc.contributor.authorBoyden, Edward Stuart
dc.date.accessioned2012-04-13T16:59:59Z
dc.date.available2012-04-13T16:59:59Z
dc.date.issued2011-04
dc.identifier.issn1662-5137
dc.identifier.urihttp://hdl.handle.net/1721.1/70022
dc.description.abstractTechnologies for silencing the electrical activity of genetically targeted neurons in the brain are important for assessing the contribution of specific cell types and pathways toward behaviors and pathologies. Recently we found that archaerhodopsin-3 from Halorubrum sodomense (Arch), a light-driven outward proton pump, when genetically expressed in neurons, enables them to be powerfully, transiently, and repeatedly silenced in response to pulses of light. Because of the impressive characteristics of Arch, we explored the optogenetic utility of opsins with high sequence homology to Arch, from archaea of the Halorubrum genus. We found that the archaerhodopsin from Halorubrum strain TP009, which we named ArchT, could mediate photocurrents of similar maximum amplitude to those of Arch (∼900 pA in vitro), but with a >3-fold improvement in light sensitivity over Arch, most notably in the optogenetic range of 1–10 mW/mm2, equating to >2× increase in brain tissue volume addressed by a typical single optical fiber. Upon expression in mouse or rhesus macaque cortical neurons, ArchT expressed well on neuronal membranes, including excellent trafficking for long distances down neuronal axons. The high light sensitivity prompted us to explore ArchT use in the cortex of the rhesus macaque. Optical perturbation of ArchT-expressing neurons in the brain of an awake rhesus macaque resulted in a rapid and complete (∼100%) silencing of most recorded cells, with suppressed cells achieving a median firing rate of 0 spikes/s upon illumination. A small population of neurons showed increased firing rates at long latencies following the onset of light stimulation, suggesting the existence of a mechanism of network-level neural activity balancing. The powerful net suppression of activity suggests that ArchT silencing technology might be of great use not only in the causal analysis of neural circuits, but may have therapeutic applications.en_US
dc.description.sponsorshipHelen Hay Whitney Foundationen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH K99MH085944)en_US
dc.description.sponsorshipMcGovern Institute Neurotechnology (MINT) Programen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Director’s New Innovator Award 1DP2OD002002, 1R01DA029639, 1R43NS070453, 1RC2DE020919, 1R01NS067199)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (NSF (EFRI 0835878))en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (DMS 0848804)en_US
dc.description.sponsorshipUnited States. Dept. of Defenseen_US
dc.description.sponsorshipBrain & Behavior Research Foundationen_US
dc.description.sponsorshipAlfred P. Sloan Foundationen_US
dc.description.sponsorshipDr. Gerald Burnett and Marjorie Burnetten_US
dc.description.sponsorshipSFN Research Award for Innovation in Neuroscienceen_US
dc.description.sponsorshipMassachusetts Institute of Technology. Media Laboratoryen_US
dc.description.sponsorshipMcGovern Institute for Brain Research at MITen_US
dc.description.sponsorshipBenesse Foundationen_US
dc.description.sponsorshipMassachusetts Institute of Technology (Neurotechnology Fund)en_US
dc.description.sponsorshipWallace H. Coulter Foundationen_US
dc.language.isoen_US
dc.publisherFrontiers Research Foundationen_US
dc.relation.isversionofhttp://dx.doi.org/10.3389/fnsys.2011.00018en_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.sourceFrontiersen_US
dc.titleA high-light sensitivity optical neural silencer: development and application to optogenetic control of non-human primate cortexen_US
dc.typeArticleen_US
dc.identifier.citationHan, Xue et al. “A High-Light Sensitivity Optical Neural Silencer: Development and Application to Optogenetic Control of Non-Human Primate Cortex.” Frontiers in Systems Neuroscience 5 (2011): 1-8.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Synthetic Neurobiology Groupen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Media Laboratoryen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.departmentProgram in Media Arts and Sciences (Massachusetts Institute of Technology)en_US
dc.contributor.approverDesimone, Robert
dc.contributor.mitauthorHan, Xue
dc.contributor.mitauthorChow, Brian Y.
dc.contributor.mitauthorZhou, Huihui
dc.contributor.mitauthorKlapoetke, Nathan Cao
dc.contributor.mitauthorChuong, Amy S.
dc.contributor.mitauthorRajimehr, Reza
dc.contributor.mitauthorYang, Aimei
dc.contributor.mitauthorBaratta, Michael V.
dc.contributor.mitauthorWinkle, Jonathan Andrew
dc.contributor.mitauthorDesimone, Robert
dc.contributor.mitauthorBoyden, Edward Stuart
dc.relation.journalFrontiers in Systems 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.orderedauthorsHan, Xue; Chow, Brian Y.; Zhou, Huihui; Klapoetke, Nathan C.; Chuong, Amy; Rajimehr, Reza; Yang, Aimei; Baratta, Michael V.; Winkle, Jonathan; Desimone, Robert; Boyden, Edward S.en
dc.identifier.orcidhttps://orcid.org/0000-0002-8860-5914
dc.identifier.orcidhttps://orcid.org/0000-0003-3466-8706
dc.identifier.orcidhttps://orcid.org/0000-0002-0419-3351
dc.identifier.orcidhttps://orcid.org/0000-0002-5938-4227
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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