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dc.contributor.authorSubach, Oksana M.
dc.contributor.authorSotskov, Vladimir P.
dc.contributor.authorPlusnin, Viktor V.
dc.contributor.authorGruzdeva, Anna M.
dc.contributor.authorBarykina, Natalia V.
dc.contributor.authorIvashkina, Olga I.
dc.contributor.authorAnokhin, Konstantin V.
dc.contributor.authorNikolaeva, Alena Y.
dc.contributor.authorKorzhenevskiy, Dmitry A.
dc.contributor.authorVlaskina, Anna V.
dc.contributor.authorLazarenko, Vladimir A.
dc.contributor.authorBoyko, Konstantin M.
dc.contributor.authorRakitina, Tatiana V.
dc.contributor.authorVarizhuk, Anna M.
dc.contributor.authorPozmogova, Galina E.
dc.contributor.authorPodgorny, Oleg V.
dc.contributor.authorPiatkevich, Kiryl
dc.contributor.authorBoyden, Edward
dc.contributor.authorSubach, Fedor V.
dc.date.accessioned2020-05-18T21:16:48Z
dc.date.available2020-05-18T21:16:48Z
dc.date.issued2020-02
dc.date.submitted2020-02
dc.identifier.issn1422-0067
dc.identifier.urihttps://hdl.handle.net/1721.1/125303
dc.description.abstractGreen fluorescent genetically encoded calcium indicators (GECIs) are the most popular tool for visualization of calcium dynamics in vivo. However, most of them are based on the EGFP protein and have similar molecular brightnesses. The NTnC indicator, which is composed of the mNeonGreen fluorescent protein with the insertion of troponin C, has higher brightness as compared to EGFP-based GECIs, but shows a limited inverted response with an ΔF/F of 1. By insertion of a calmodulin/M13-peptide pair into the mNeonGreen protein, we developed a green GECI called NCaMP7. In vitro, NCaMP7 showed positive response with an ΔF/F of 27 and high affinity (Kd of 125 nM) to calcium ions. NCaMP7 demonstrated a 1.7-fold higher brightness and similar calcium-association/dissociation dynamics compared to the standard GCaMP6s GECI in vitro. According to fluorescence recovery after photobleaching (FRAP) experiments, the NCaMP7 design partially prevented interactions of NCaMP7 with the intracellular environment. The NCaMP7 crystal structure was obtained at 1.75 Å resolution to uncover the molecular basis of its calcium ions sensitivity. The NCaMP7 indicator retained a high and fast response when expressed in cultured HeLa and neuronal cells. Finally, we successfully utilized the NCaMP7 indicator for in vivo visualization of grating-evoked and place-dependent neuronal activity in the visual cortex and the hippocampus of mice using a two-photon microscope and an NVista miniscope, respectively.en_US
dc.language.isoen
dc.publisherMDPI AGen_US
dc.relation.isversionofhttp://dx.doi.org/10.3390/ijms21051644en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceMDPIen_US
dc.titleNovel Genetically Encoded Bright Positive Calcium Indicator NCaMP7 Based on the mNeonGreen Fluorescent Proteinen_US
dc.typeArticleen_US
dc.identifier.citationSubach, Oksana et al. "Novel Genetically Encoded Bright Positive Calcium Indicator NCaMP7 Based on the mNeonGreen Fluorescent Protein." International Journal of Molecular Sciences 21, 5: 1644 © 2020 Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Media Laboratory
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciences
dc.contributor.departmentProgram in Media Arts and Sciences (Massachusetts Institute of Technology)
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.relation.journalInternational Journal of Molecular Sciencesen_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.updated2020-03-24T14:45:27Z
dspace.date.submission2020-03-24T14:47:38Z
mit.journal.volume21en_US
mit.journal.issue5en_US
mit.licensePUBLISHER_CC
mit.metadata.statusComplete


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