Jensen, Nickels A.

[["dc.bibliographiccitation.artnumber","4762"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Nature Communications"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Kamper, Maria"],["dc.contributor.author","Ta, Haisen"],["dc.contributor.author","Jensen, Nickels A."],["dc.contributor.author","Hell, Stefan W."],["dc.contributor.author","Jakobs, Stefan"],["dc.date.accessioned","2019-07-09T11:50:56Z"],["dc.date.available","2019-07-09T11:50:56Z"],["dc.date.issued","2018"],["dc.description.abstract","The near infrared (NIR) optical window between the cutoff for hemoglobin absorption at 650 nm and the onset of increased water absorption at 900 nm is an attractive, yet largely unexplored, spectral regime for diffraction-unlimited super-resolution fluorescence microscopy (nanoscopy). We developed the NIR fluorescent protein SNIFP, a bright and photostable bacteriophytochrome, and demonstrate its use as a fusion tag in live-cell microscopy and STED nanoscopy. We further demonstrate dual color red-confocal/NIR-STED imaging by co-expressing SNIFP with a conventional red fluorescent protein."],["dc.identifier.doi","10.1038/s41467-018-07246-2"],["dc.identifier.pmid","30420676"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16027"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/59855"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.subject.ddc","610"],["dc.title","Near-infrared STED nanoscopy with an engineered bacterial phytochrome"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","ChemPhysChem"],["dc.contributor.author","Adam, Virgile"],["dc.contributor.author","Hadjidemetriou, Kyprianos"],["dc.contributor.author","Jensen, Nickels"],["dc.contributor.author","Shoeman, Robert L."],["dc.contributor.author","Woodhouse, Joyce"],["dc.contributor.author","Aquila, Andrew"],["dc.contributor.author","Banneville, Anne‐Sophie"],["dc.contributor.author","Barends, Thomas R. M."],["dc.contributor.author","Bezchastnov, Victor"],["dc.contributor.author","Boutet, Sébastien"],["dc.contributor.author","Weik, Martin"],["dc.date.accessioned","2022-09-01T09:49:35Z"],["dc.date.available","2022-09-01T09:49:35Z"],["dc.date.issued","2022"],["dc.description.sponsorship"," Basic Energy Sciences https://doi.org/10.13039/100006151"],["dc.description.sponsorship"," National Institutes of Health https://doi.org/10.13039/100000002"],["dc.description.sponsorship"," Max-Planck-Gesellschaft https://doi.org/10.13039/501100004189"],["dc.identifier.doi","10.1002/cphc.202200192"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/113470"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-597"],["dc.relation.eissn","1439-7641"],["dc.relation.issn","1439-4235"],["dc.rights.uri","http://creativecommons.org/licenses/by-nc/4.0/"],["dc.title","Rational Control of Off‐State Heterogeneity in a Photoswitchable Fluorescent Protein Provides Switching Contrast Enhancement**"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Communications Biology"],["dc.bibliographiccitation.volume","3"],["dc.contributor.author","Ruhlandt, Daja"],["dc.contributor.author","Andresen, Martin"],["dc.contributor.author","Jensen, Nickels"],["dc.contributor.author","Gregor, Ingo"],["dc.contributor.author","Jakobs, Stefan"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Chizhik, Alexey I."],["dc.date.accessioned","2021-03-05T08:58:32Z"],["dc.date.available","2021-03-05T08:58:32Z"],["dc.date.issued","2020"],["dc.description.sponsorship","Open-Access-Publikationsfonds 2021"],["dc.identifier.doi","10.1038/s42003-020-01316-2"],["dc.identifier.pmid","33128009"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17780"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/80175"],["dc.identifier.url","https://mbexc.uni-goettingen.de/literature/publications/87"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-393"],["dc.notes.intern","Merged from goescholar"],["dc.relation","EXC 2067: Multiscale Bioimaging"],["dc.relation.eissn","2399-3642"],["dc.relation.orgunit","Fakultät für Physik"],["dc.relation.workinggroup","RG Enderlein"],["dc.relation.workinggroup","RG Jakobs (Structure and Dynamics of Mitochondria)"],["dc.rights","CC BY 4.0"],["dc.rights.uri","http://creativecommons.org/licenses/by/4.0/"],["dc.title","Absolute quantum yield measurements of fluorescent proteins using a plasmonic nanocavity"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","756"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","ChemPhysChem"],["dc.bibliographiccitation.lastpage","762"],["dc.bibliographiccitation.volume","15"],["dc.contributor.author","Jensen, Nickels A."],["dc.contributor.author","Danzl, Johann G."],["dc.contributor.author","Willig, Katrin I."],["dc.contributor.author","Lavoie-Cardinal, Flavie"],["dc.contributor.author","Brakemann, Tanja"],["dc.contributor.author","Hell, Stefan W."],["dc.contributor.author","Jakobs, Stefan"],["dc.date.accessioned","2017-09-07T11:46:25Z"],["dc.date.available","2017-09-07T11:46:25Z"],["dc.date.issued","2014"],["dc.description.abstract","Diffraction-unlimited far-field super-resolution fluorescence (nanoscopy) methods typically rely on transiently transferring fluorophores between two states, whereby this transfer is usually laid out as a switch. However, depending on whether this is induced in a spatially controlled manner using a pattern of light (coordinate-targeted) or stochastically on a single-molecule basis, specific requirements on the fluorophores are imposed. Therefore, the fluorophores are usually utilized just for one class of methods only. In this study we demonstrate that the reversibly switchable fluorescent protein Dreiklang enables live-cell recordings in both spatially controlled and stochastic modes. We show that the Dreiklang chromophore entails three different light-induced switching mechanisms, namely a reversible photochemical one, off-switching by stimulated emission, and a reversible transfer to a long-lived dark state from the S-1 state, all of which can be utilized to overcome the diffraction barrier. We also find that for the single-molecule-based stochastic GSDIM approach (ground-state depletion followed by individual molecule return), Dreiklang provides a larger number of on-off localization events as compared to its progenitor Citrine. Altogether, Dreiklang is a versatile probe for essentially all popular forms of live-cell fluorescence nanoscopy."],["dc.identifier.doi","10.1002/cphc.201301034"],["dc.identifier.gro","3142169"],["dc.identifier.isi","000332747500026"],["dc.identifier.pmid","24497300"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/5299"],["dc.language.iso","en"],["dc.notes.intern","WoS Import 2017-03-10"],["dc.notes.status","final"],["dc.notes.submitter","PUB_WoS_Import"],["dc.relation.eissn","1439-7641"],["dc.relation.issn","1439-4235"],["dc.title","Coordinate-Targeted and Coordinate-Stochastic Super-Resolution Microscopy with the Reversibly Switchable Fluorescent Protein Dreiklang"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.subtype","original"],["dspace.entity.type","Publication"]]

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[["dc.bibliographiccitation.firstpage","20992"],["dc.bibliographiccitation.issue","49"],["dc.bibliographiccitation.journal","Proceedings of the National Academy of Sciences"],["dc.bibliographiccitation.lastpage","20997"],["dc.bibliographiccitation.volume","107"],["dc.contributor.author","Bohn, S."],["dc.contributor.author","Beck, F."],["dc.contributor.author","Sakata, E."],["dc.contributor.author","Walzthoeni, T."],["dc.contributor.author","Beck, M."],["dc.contributor.author","Aebersold, R."],["dc.contributor.author","Forster, F."],["dc.contributor.author","Baumeister, W."],["dc.contributor.author","Nickell, S."],["dc.date.accessioned","2022-03-01T11:46:22Z"],["dc.date.available","2022-03-01T11:46:22Z"],["dc.date.issued","2010"],["dc.identifier.doi","10.1073/pnas.1015530107"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/103646"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-531"],["dc.relation.eissn","1091-6490"],["dc.relation.issn","0027-8424"],["dc.title","Structure of the 26S proteasome from Schizosaccharomyces pombe at subnanometer resolution"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","655"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","ChemPhysChem"],["dc.bibliographiccitation.lastpage","663"],["dc.bibliographiccitation.volume","15"],["dc.contributor.author","Lavoie-Cardinal, Flavie"],["dc.contributor.author","Jensen, Nickels A."],["dc.contributor.author","Westphal, Volker"],["dc.contributor.author","Stiel, Andre C."],["dc.contributor.author","Chmyrov, Andriy"],["dc.contributor.author","Bierwagen, Jakob"],["dc.contributor.author","Testa, Ilaria"],["dc.contributor.author","Jakobs, Stefan"],["dc.contributor.author","Hell, Stefan W."],["dc.date.accessioned","2017-09-07T11:46:25Z"],["dc.date.available","2017-09-07T11:46:25Z"],["dc.date.issued","2014"],["dc.description.abstract","Up to now, all demonstrations of reversible saturable optical fluorescence transitions (RESOLFT) superresolution microscopy of living cells have relied on the use of reversibly switchable fluorescent proteins (RSFP) emitting in the green spectral range. Here we show RESOLFT imaging with rsCherryRev1.4, a new red-emitting RSFP enabling a spatial resolution up to four times higher than the diffraction barrier. By co-expressing green and red RSFPs in living cells we demonstrate two-color RESOLFT imaging both for single (donut) beam scanning and for parallelized versions of RESOLFT nanoscopy where an array of >23000 donut-like minima are scanned simultaneously."],["dc.identifier.doi","10.1002/cphc.201301016"],["dc.identifier.gro","3142168"],["dc.identifier.isi","000332747500013"],["dc.identifier.pmid","24449030"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/12826"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/5288"],["dc.language.iso","en"],["dc.notes.intern","WoS Import 2017-03-10 / Funder: Deutsche Forschungsgemeinschaft"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","final"],["dc.notes.submitter","PUB_WoS_Import"],["dc.relation.eissn","1439-7641"],["dc.relation.issn","1439-4235"],["dc.rights","CC BY-NC-ND 3.0"],["dc.rights.uri","https://creativecommons.org/licenses/by-nc-nd/3.0"],["dc.title","Two-Color RESOLFT Nanoscopy with Green and Red Fluorescent Photochromic Proteins"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.subtype","original"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","9509"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","ACS Nano"],["dc.bibliographiccitation.lastpage","9521"],["dc.bibliographiccitation.volume","15"],["dc.contributor.author","Konen, Timo"],["dc.contributor.author","Stumpf, Daniel"],["dc.contributor.author","Grotjohann, Tim"],["dc.contributor.author","Jansen, Isabelle"],["dc.contributor.author","Bossi, Mariano"],["dc.contributor.author","Weber, Michael"],["dc.contributor.author","Jensen, Nickels"],["dc.contributor.author","Hell, Stefan W."],["dc.contributor.author","Jakobs, Stefan"],["dc.date.accessioned","2021-08-12T07:44:53Z"],["dc.date.available","2021-08-12T07:44:53Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1021/acsnano.0c08207"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/88319"],["dc.identifier.url","https://rdp.sfb274.de/literature/publications/34"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-448"],["dc.relation","TRR 274: Checkpoints of Central Nervous System Recovery"],["dc.relation","TRR 274 | Z01: Bioimaging Platform"],["dc.relation.eissn","1936-086X"],["dc.relation.issn","1936-0851"],["dc.relation.workinggroup","RG Jakobs (Structure and Dynamics of Mitochondria)"],["dc.title","The Positive Switching Fluorescent Protein Padron2 Enables Live-Cell Reversible Saturable Optical Linear Fluorescence Transitions (RESOLFT) Nanoscopy without Sequential Illumination Steps"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1479"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","Proceedings of the National Academy of Sciences"],["dc.bibliographiccitation.lastpage","1484"],["dc.bibliographiccitation.volume","109"],["dc.contributor.author","Sakata, E."],["dc.contributor.author","Bohn, S."],["dc.contributor.author","Mihalache, O."],["dc.contributor.author","Kiss, P."],["dc.contributor.author","Beck, F."],["dc.contributor.author","Nagy, I."],["dc.contributor.author","Nickell, S."],["dc.contributor.author","Tanaka, K."],["dc.contributor.author","Saeki, Y."],["dc.contributor.author","Forster, F."],["dc.contributor.author","Baumeister, W."],["dc.date.accessioned","2022-03-01T11:46:23Z"],["dc.date.available","2022-03-01T11:46:23Z"],["dc.date.issued","2012"],["dc.identifier.doi","10.1073/pnas.1119394109"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/103649"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-531"],["dc.relation.eissn","1091-6490"],["dc.relation.issn","0027-8424"],["dc.title","Localization of the proteasomal ubiquitin receptors Rpn10 and Rpn13 by electron cryomicroscopy"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","14870"],["dc.bibliographiccitation.issue","37"],["dc.bibliographiccitation.journal","Proceedings of the National Academy of Sciences"],["dc.bibliographiccitation.lastpage","14875"],["dc.bibliographiccitation.volume","109"],["dc.contributor.author","Beck, F."],["dc.contributor.author","Unverdorben, P."],["dc.contributor.author","Bohn, S."],["dc.contributor.author","Schweitzer, A."],["dc.contributor.author","Pfeifer, G."],["dc.contributor.author","Sakata, E."],["dc.contributor.author","Nickell, S."],["dc.contributor.author","Plitzko, J. M."],["dc.contributor.author","Villa, E."],["dc.contributor.author","Baumeister, W."],["dc.contributor.author","Forster, F."],["dc.date.accessioned","2022-03-01T11:46:23Z"],["dc.date.available","2022-03-01T11:46:23Z"],["dc.date.issued","2012"],["dc.identifier.doi","10.1073/pnas.1213333109"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/103650"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-531"],["dc.relation.eissn","1091-6490"],["dc.relation.issn","0027-8424"],["dc.title","Near-atomic resolution structural model of the yeast 26S proteasome"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]