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dc.contributor.authorQian, Yong
dc.contributor.authorCosio, Danielle M. Orozco
dc.contributor.authorPiatkevich, Kiryl D.
dc.contributor.authorAufmkolk, Sarah
dc.contributor.authorSu, Wan-Chi
dc.contributor.authorCeliker, Orhan T.
dc.contributor.authorSchohl, Anne
dc.contributor.authorMurdock, Mitchell H.
dc.contributor.authorAggarwal, Abhi
dc.contributor.authorChang, Yu-Fen
dc.contributor.authorWiseman, Paul W.
dc.contributor.authorRuthazer, Edward S.
dc.contributor.authorBoyden, Edward S.
dc.contributor.authorCampbell, Robert E.
dc.date.accessioned2022-06-13T15:05:55Z
dc.date.available2021-10-27T19:57:46Z
dc.date.available2022-06-13T15:05:55Z
dc.date.issued2020-11
dc.date.submitted2020-04
dc.identifier.issn1545-7885
dc.identifier.urihttps://hdl.handle.net/1721.1/134043.2
dc.description.abstract© 2020 Qian et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Near-infrared (NIR) genetically encoded calcium ion (Ca2+) indicators (GECIs) can provide advantages over visible wavelength fluorescent GECIs in terms of reduced phototoxicity, minimal spectral cross talk with visible light excitable optogenetic tools and fluorescent probes, and decreased scattering and absorption in mammalian tissues. Our previously reported NIR GECI, NIR-GECO1, has these advantages but also has several disadvantages including lower brightness and limited fluorescence response compared to state-of-the-art visible wavelength GECIs, when used for imaging of neuronal activity. Here, we report 2 improved NIR GECI variants, designated NIR-GECO2 and NIR-GECO2G, derived from NIR-GECO1. We characterized the performance of the new NIR GECIs in cultured cells, acute mouse brain slices, and Caenorhabditis elegans and Xenopus laevis in vivo. Our results demonstrate that NIR-GECO2 and NIR-GECO2G provide substantial improvements over NIR-GECO1 for imaging of neuronal Ca2+ dynamics.en_US
dc.language.isoen
dc.publisherPublic Library of Science (PLoS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pbio.3000965en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourcePLoSen_US
dc.titleImproved genetically encoded near-infrared fluorescent calcium ion indicators for in vivo imagingen_US
dc.typeArticleen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.contributor.departmentProgram in Media Arts and Sciences (Massachusetts Institute of Technology)
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciences
dc.contributor.departmentMcGovern Institute for Brain Research at MIT
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Center for Neurobiological Engineering
dc.contributor.departmentHoward Hughes Medical Institute
dc.relation.journalPLoS Biologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-03-12T15:47:32Z
dspace.orderedauthorsQian, Y; Cosio, DMO; Piatkevich, KD; Aufmkolk, S; Su, W-C; Celiker, OT; Schohl, A; Murdock, MH; Aggarwal, A; Chang, Y-F; Wiseman, PW; Ruthazer, ES; Boyden, ES; Campbell, REen_US
dspace.date.submission2021-03-12T15:47:34Z
mit.journal.volume18en_US
mit.journal.issue11en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work Neededen_US


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