Enderlein, Jörg

[["dc.bibliographiccitation.issue","36"],["dc.bibliographiccitation.journal","Nanotechnology"],["dc.bibliographiccitation.volume","33"],["dc.contributor.affiliation","Ghosh, Subhabrata;"],["dc.contributor.affiliation","Hollingsworth, Jennifer A;"],["dc.contributor.affiliation","Gallea, Jose Ignacio;"],["dc.contributor.affiliation","Majumder, Somak;"],["dc.contributor.affiliation","Enderlein, Jörg;"],["dc.contributor.affiliation","Chizhik, Alexey I;"],["dc.contributor.author","Ghosh, Subhabrata"],["dc.contributor.author","Hollingsworth, Jennifer"],["dc.contributor.author","Gallea, Jose Ignacio"],["dc.contributor.author","Majumder, Somak"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Chizhik, Alexey"],["dc.date.accessioned","2022-06-01T09:39:18Z"],["dc.date.available","2022-06-01T09:39:18Z"],["dc.date.issued","2022"],["dc.date.updated","2022-06-17T02:42:41Z"],["dc.description.abstract","Abstract We report on proof of principle measurements of a concept for a super-resolution imaging method that is based on excitation field density-dependent lifetime modulation of semiconductor nanocrystals. The prerequisite of the technique is access to semiconductor nanocrystals with emission lifetimes that depend on the excitation intensity. Experimentally, the method requires a confocal microscope with fluorescence-lifetime measurement capability that makes it easily accessible to a broad optical imaging community. We demonstrate with single particle imaging that the method allows one to achieve a spatial resolution of the order of several tens of nanometers at moderate fluorescence excitation intensity."],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft https://doi.org/10.13039/501100001659"],["dc.description.sponsorship","H2020 European Research Council https://doi.org/10.13039/100010663"],["dc.description.sponsorship","Office of Energy Efficiency and Renewable Energy https://doi.org/10.13039/100006134"],["dc.identifier.doi","10.1088/1361-6528/ac73a2"],["dc.identifier.pmid","35617874"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/108438"],["dc.identifier.url","https://mbexc.uni-goettingen.de/literature/publications/491"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-572"],["dc.relation","EXC 2067: Multiscale Bioimaging"],["dc.relation.eissn","1361-6528"],["dc.relation.issn","0957-4484"],["dc.relation.workinggroup","RG Enderlein"],["dc.rights.uri","http://creativecommons.org/licenses/by/4.0/"],["dc.title","Excited state lifetime modulation in semiconductor nanocrystals for super-resolution imaging"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","Biophysical Journal"],["dc.contributor.author","Yudovich, Shimon"],["dc.contributor.author","Marzouqe, Adan"],["dc.contributor.author","Kantorovitsch, Joseph"],["dc.contributor.author","Teblum, Eti"],["dc.contributor.author","Chen, Tao"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Miller, Evan W."],["dc.contributor.author","Weiss, Shimon"],["dc.date.accessioned","2022-06-01T09:40:11Z"],["dc.date.available","2022-06-01T09:40:11Z"],["dc.date.issued","2022"],["dc.description.abstract","Supported lipid bilayers are a well-developed model system for the study of membranes and their associated proteins, such as membrane channels, enzymes, and receptors. These versatile model membranes can be made from various components, ranging from simple synthetic phospholipids to complex mixtures of constituents, mimicking the cell membrane with its relevant physiochemical and molecular phenomena. In addition, the high stability of supported lipid bilayers allows for their study via a wide array of experimental probes. In this work, we describe a platform for supported lipid bilayers that is accessible both electrically and optically, and demonstrate direct optical observation of the transmembrane potential of supported lipid bilayers. We show that the polarization of the supported membrane can be electrically controlled and optically probed using voltage-sensitive dyes. Membrane polarization dynamics is understood through electrochemical impedance spectroscopy and the analysis of an equivalent electrical circuit model. In addition, we describe the effect of the conducting electrode layer on the fluorescence of the optical probe through metal-induced energy transfer, and show that while this energy transfer has an adverse effect on the voltage sensitivity of the fluorescent probe, its strong distance dependency allows for axial localization of fluorescent emitters with ultrahigh accuracy. We conclude with a discussion on possible applications of this platform for the study of voltage-dependent membrane proteins and other processes in membrane biology and surface science."],["dc.identifier.doi","10.1016/j.bpj.2022.05.037"],["dc.identifier.pii","S0006349522004301"],["dc.identifier.pmid","35619563"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/108658"],["dc.identifier.url","https://mbexc.uni-goettingen.de/literature/publications/494"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-572"],["dc.relation","EXC 2067: Multiscale Bioimaging"],["dc.relation.issn","0006-3495"],["dc.relation.workinggroup","RG Enderlein"],["dc.rights","CC BY-ND 4.0"],["dc.title","Electrically Controlling and Optically Observing the Membrane Potential of Supported Lipid Bilayers"],["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","38"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Communications Biology"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Oleksiievets, Nazar"],["dc.contributor.author","Sargsyan, Yelena"],["dc.contributor.author","Thiele, Jan Christoph"],["dc.contributor.author","Mougios, Nikolaos"],["dc.contributor.author","Sograte-Idrissi, Shama"],["dc.contributor.author","Nevskyi, Oleksii"],["dc.contributor.author","Gregor, Ingo"],["dc.contributor.author","Opazo, Felipe"],["dc.contributor.author","Thoms, Sven"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Tsukanov, Roman"],["dc.date.accessioned","2022-01-13T06:27:32Z"],["dc.date.available","2022-01-13T06:27:32Z"],["dc.date.issued","2022-01-11"],["dc.description.abstract","DNA point accumulation for imaging in nanoscale topography (DNA-PAINT) is a powerful super-resolution technique highly suitable for multi-target (multiplexing) bio-imaging. However, multiplexed imaging of cells is still challenging due to the dense and sticky environment inside a cell. Here, we combine fluorescence lifetime imaging microscopy (FLIM) with DNA-PAINT and use the lifetime information as a multiplexing parameter for targets identification. In contrast to Exchange-PAINT, fluorescence lifetime PAINT (FL-PAINT) can image multiple targets simultaneously and does not require any fluid exchange, thus leaving the sample undisturbed and making the use of flow chambers/microfluidic systems unnecessary. We demonstrate the potential of FL-PAINT by simultaneous imaging of up to three targets in a cell using both wide-field FLIM and 3D time-resolved confocal laser scanning microscopy (CLSM). FL-PAINT can be readily combined with other existing techniques of multiplexed imaging and is therefore a perfect candidate for high-throughput multi-target bio-imaging."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2022"],["dc.identifier.doi","10.1038/s42003-021-02976-4"],["dc.identifier.pmid","35017652"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/98096"],["dc.identifier.url","https://mbexc.uni-goettingen.de/literature/publications/392"],["dc.identifier.url","https://sfb1002.med.uni-goettingen.de/production/literature/publications/415"],["dc.language.iso","en"],["dc.relation","EXC 2067: Multiscale Bioimaging"],["dc.relation","SFB 1002: Modulatorische Einheiten bei Herzinsuffizienz"],["dc.relation","SFB 1002 | A10: Peroxisomen als modulatorische Einheiten im Herzstoffwechsel und bei Herzinsuffizienz"],["dc.relation.issn","2399-3642"],["dc.relation.orgunit","III. Physikalisches Institut - Biophysik"],["dc.relation.workinggroup","RG Enderlein"],["dc.relation.workinggroup","RG Thoms (Biochemistry and Molecular Medicine)"],["dc.rights","CC BY 4.0"],["dc.title","Fluorescence lifetime DNA-PAINT for multiplexed super-resolution imaging of cells"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","055016"],["dc.bibliographiccitation.firstpage","1"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","New Journal of Physics"],["dc.bibliographiccitation.lastpage","10"],["dc.bibliographiccitation.volume","13"],["dc.contributor.author","Marshall, Graham D."],["dc.contributor.author","Gaebel, Torsten"],["dc.contributor.author","Matthews, Jonathan C. F."],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","O’Brien, Jeremy L."],["dc.contributor.author","Rabeau, James R."],["dc.date.accessioned","2018-04-23T11:49:31Z"],["dc.date.available","2018-04-23T11:49:31Z"],["dc.date.issued","2011"],["dc.description.abstract","On-demand, high repetition rate sources of indistinguishable, polarized single photons are the key component for future photonic quantum technologies (O'Brien et al 2009 Nat. Photonics 3 687–95). Colour centres in diamond offer a promising solution, and the narrow linewidth of the recently identified nickel-based NE8 centre makes it particularly appealing for realizing the transform-limited sources necessary for quantum interference. Here, we report the characterization of dipole orientation and coherence properties of a single NE8 colour centre in a diamond nanocrystal at room temperature. We observe a single-photon coherence time of 0.21 ps and an emission lifetime of 1.5 ns. Combined with an emission wavelength that is ideally suited for applications in existing quantum optical systems, these results show that NE8 is a far more promising source than the more commonly studied nitrogen-vacancy centre and point the way to the realization of a practical diamond colour centre-based single-photon source."],["dc.identifier.doi","10.1088/1367-2630/13/5/055016"],["dc.identifier.fs","590726"],["dc.identifier.gro","3142139"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/8628"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/13721"],["dc.language.iso","en"],["dc.notes.intern","lifescience updates Crossref Import"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","final"],["dc.relation.doi","10.1088/1367-2630/13/5/055016"],["dc.relation.issn","1367-2630"],["dc.relation.issn","1367-2630"],["dc.relation.orgunit","Fakultät für Physik"],["dc.title","Coherence properties of a single dipole emitter in diamond"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","no"],["dc.type.version","published_version"],["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","6310"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","6313"],["dc.bibliographiccitation.volume","60"],["dc.contributor.author","Glogger, Marius"],["dc.contributor.author","Spahn, Christoph"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Heilemann, Mike"],["dc.date.accessioned","2021-04-14T08:29:30Z"],["dc.date.available","2021-04-14T08:29:30Z"],["dc.date.issued","2021"],["dc.description.abstract","Abstract Super‐resolution optical fluctuation imaging (SOFI) is a super‐resolution microscopy technique that overcomes the diffraction limit by analyzing intensity fluctuations of statistically independent emitters in a time series of images. The final images are background‐free and show confocality and enhanced spatial resolution (super‐resolution). Fluorophore photobleaching, however, is a key limitation for recording long time series of images that will allow for the calculation of higher order SOFI results with correspondingly increased resolution. Here, we demonstrate that photobleaching can be circumvented by using fluorophore labels that reversibly and transiently bind to a target, and which are being replenished from a buffer which serves as a reservoir. Using fluorophore‐labeled short DNA oligonucleotides, we labeled cellular structures with target‐specific antibodies that contain complementary DNA sequences and record the fluctuation events caused by transient emitter binding. We show that this concept bypasses extensive photobleaching and facilitates two‐color imaging of cellular structures with SOFI."],["dc.description.abstract","Fluorophore labels that transiently bind to and unbind from a protein target allow photobleaching in super‐resolution optical fluctuation imaging (SOFI) to be circumvented. Using short fluorophore‐labeled DNA oligonucleotides, we demonstrate high‐contrast, low‐background, and multi‐color super‐resolution imaging with SOFI. image"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659"],["dc.identifier.doi","10.1002/anie.202013166"],["dc.identifier.pmid","33301653"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82919"],["dc.identifier.url","https://mbexc.uni-goettingen.de/literature/publications/131"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation","EXC 2067: Multiscale Bioimaging"],["dc.relation.eissn","1521-3773"],["dc.relation.issn","1433-7851"],["dc.relation.workinggroup","RG Enderlein"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited."],["dc.title","Multi‐Color, Bleaching‐Resistant Super‐Resolution Optical Fluctuation Imaging with Oligonucleotide‐Based Exchangeable Fluorophores"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","169"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Nanophotonics"],["dc.bibliographiccitation.lastpage","202"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Koenderink, A. Femius"],["dc.contributor.author","Tsukanov, Roman"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Izeddin, Ignacio"],["dc.contributor.author","Krachmalnicoff, Valentina"],["dc.date.accessioned","2022-02-01T10:31:35Z"],["dc.date.available","2022-02-01T10:31:35Z"],["dc.date.issued","2021"],["dc.description.abstract","Abstract Probing light–matter interaction at the nanometer scale is one of the most fascinating topics of modern optics. Its importance is underlined by the large span of fields in which such accurate knowledge of light–matter interaction is needed, namely nanophotonics, quantum electrodynamics, atomic physics, biosensing, quantum computing and many more. Increasing innovations in the field of microscopy in the last decade have pushed the ability of observing such phenomena across multiple length scales, from micrometers to nanometers. In bioimaging, the advent of super-resolution single-molecule localization microscopy (SMLM) has opened a completely new perspective for the study and understanding of molecular mechanisms, with unprecedented resolution, which take place inside the cell. Since then, the field of SMLM has been continuously improving, shifting from an initial drive for pushing technological limitations to the acquisition of new knowledge. Interestingly, such developments have become also of great interest for the study of light–matter interaction in nanostructured materials, either dielectric, metallic, or hybrid metallic-dielectric. The purpose of this review is to summarize the recent advances in the field of nanophotonics that have leveraged SMLM, and conversely to show how some concepts commonly used in nanophotonics can benefit the development of new microscopy techniques for biophysics. To this aim, we will first introduce the basic concepts of SMLM and the observables that can be measured. Then, we will link them with their corresponding physical quantities of interest in biophysics and nanophotonics and we will describe state-of-the-art experiments that apply SMLM to nanophotonics. The problem of localization artifacts due to the interaction of the fluorescent emitter with a resonant medium and possible solutions will be also discussed. Then, we will show how the interaction of fluorescent emitters with plasmonic structures can be successfully employed in biology for cell profiling and membrane organization studies. We present an outlook on emerging research directions enabled by the synergy of localization microscopy and nanophotonics."],["dc.identifier.doi","10.1515/nanoph-2021-0551"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/98897"],["dc.identifier.url","https://mbexc.uni-goettingen.de/literature/publications/375"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-517"],["dc.relation","EXC 2067: Multiscale Bioimaging"],["dc.relation.eissn","2192-8614"],["dc.relation.workinggroup","RG Enderlein"],["dc.rights","CC BY 4.0"],["dc.title","Super-resolution imaging: when biophysics meets nanophotonics"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","overview_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","4541"],["dc.bibliographiccitation.issue","15"],["dc.bibliographiccitation.journal","Nanoscale Advances"],["dc.bibliographiccitation.lastpage","4553"],["dc.bibliographiccitation.volume","3"],["dc.contributor.author","Selvaggio, Gabriele"],["dc.contributor.author","Weitzel, Milan"],["dc.contributor.author","Oleksiievets, Nazar"],["dc.contributor.author","Oswald, Tabea A."],["dc.contributor.author","Nißler, Robert"],["dc.contributor.author","Mey, Ingo"],["dc.contributor.author","Karius, Volker"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Tsukanov, Roman"],["dc.contributor.author","Kruss, Sebastian"],["dc.date.accessioned","2021-08-12T07:45:03Z"],["dc.date.available","2021-08-12T07:45:03Z"],["dc.date.issued","2021"],["dc.description.abstract","The layered silicates Egyptian Blue (CaCuSi 4 O 10 , EB), Han Blue (BaCuSi 4 O 10 , HB) and Han Purple (BaCuSi 2 O 6 , HP) emit as bulk materials bright and stable fluorescence in the near-infrared (NIR), which is of high interest for (bio)photonics due to minimal scattering, absorption and phototoxicity in this spectral range. So far the optical properties of nanosheets (NS) of these silicates are poorly understood. Here, we exfoliate them into monodisperse nanosheets, report their physicochemical properties and use them for (bio)photonics. The approach uses ball milling followed by tip sonication and centrifugation steps to exfoliate the silicates into NS with lateral size and thickness down to ≈ 16–27 nm and 1–4 nm, respectively. They emit at ≈ 927 nm (EB-NS), 953 nm (HB-NS) and 924 nm (HP-NS), and single NS can be imaged in the NIR. The fluorescence lifetimes decrease from ≈ 30–100 μs (bulk) to 17 μs (EB-NS), 8 μs (HB-NS) and 7 μs (HP-NS), thus enabling lifetime-encoded multicolor imaging both on the microscopic and the macroscopic scale. Finally, remote imaging through tissue phantoms reveals the potential for bioimaging. In summary, we report a procedure to gain monodisperse NIR fluorescent silicate nanosheets, determine their size-dependent photophysical properties and showcase the potential for NIR photonics."],["dc.identifier.doi","10.1039/D1NA00238D"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/88360"],["dc.identifier.url","https://mbexc.uni-goettingen.de/literature/publications/324"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-448"],["dc.relation","EXC 2067: Multiscale Bioimaging"],["dc.relation.eissn","2516-0230"],["dc.relation.workinggroup","RG Enderlein"],["dc.rights","CC BY 3.0"],["dc.rights.uri","http://creativecommons.org/licenses/by/3.0/"],["dc.title","Photophysical properties and fluorescence lifetime imaging of exfoliated near-infrared fluorescent silicate nanosheets"],["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","1937"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Soft Matter"],["dc.bibliographiccitation.lastpage","1946"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Sengupta, Anupam"],["dc.contributor.author","Pieper, Christoph"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Bahr, Christian"],["dc.contributor.author","Herminghaus, Stephan"],["dc.date.accessioned","2017-09-07T11:51:51Z"],["dc.date.available","2017-09-07T11:51:51Z"],["dc.date.issued","2012"],["dc.description.abstract","We study the flow of a nematic liquid crystal past a micron-sized cylindrical pillar within a microfluidic confinement of a rectangular cross-section. The liquid crystal molecules are anchored perpendicularly (homeotropic anchoring) to the surface of the pillar and the channel walls. Flow past the cylindrical obstacle generated topological defect structures whose nature, dimensions and morphology varied with the flow velocity and channel dimensions. On increasing the flow speed, we observed sequential evolution of a semi-integer loop, which transformed into an integer hedgehog defect, and finally equilibrated to an extended defect wall. On stopping the flow, the topological defect states reversed its sequence of appearance. Additionally, we introduce dual-focus fluorescence correlation spectroscopy as a general velocimetry technique for microfluidics of liquid crystal systems – with or without topological defect structures."],["dc.identifier.doi","10.1039/c2sm27337c"],["dc.identifier.gro","3146188"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10477"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/3943"],["dc.language.iso","en"],["dc.notes","This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively."],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","public"],["dc.relation","info:eu-repo/grantAgreement/EC/FP7/215851/EU//HIERARCHY"],["dc.relation.issn","1744-683X"],["dc.relation.orgunit","Fakultät für Physik"],["dc.title","Flow of a nematogen past a cylindrical micro-pillar"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","no"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","48"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Cells"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Sograte-Idrissi, Shama"],["dc.contributor.author","Oleksiievets, Nazar"],["dc.contributor.author","Isbaner, Sebastian"],["dc.contributor.author","Eggert Martínez, Mariana"],["dc.contributor.author","Enderlein, Jörg"],["dc.contributor.author","Tsukanov, Roman"],["dc.contributor.author","Opazo, Felipe"],["dc.date.accessioned","2020-12-10T18:46:58Z"],["dc.date.available","2020-12-10T18:46:58Z"],["dc.date.issued","2019"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft"],["dc.identifier.doi","10.3390/cells8010048"],["dc.identifier.eissn","2073-4409"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/78601"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.publisher","MDPI"],["dc.relation.eissn","2073-4409"],["dc.rights","https://creativecommons.org/licenses/by/4.0/"],["dc.title","Nanobody Detection of Standard Fluorescent Proteins Enables Multi-Target DNA-PAINT with High Resolution and Minimal Displacement Errors"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]