dc.contributor.author | Ahluwalia, Balpreet Singh | |
dc.contributor.author | Helle, Øystein Ivar | |
dc.contributor.author | Diekmann, Robin | |
dc.contributor.author | Øie, Cristina Ionica | |
dc.contributor.author | McCourt, Peter A. G. | |
dc.contributor.author | Schuttpelz, Mark | |
dc.date.accessioned | 2018-01-22T09:38:54Z | |
dc.date.available | 2018-01-22T09:38:54Z | |
dc.date.issued | 2017-04-24 | |
dc.description.abstract | Present optical nanoscopy techniques use a complex microscope for imaging and a simple glass slide to hold the sample. Here, we demonstrate the inverse: the use of a complex, but mass-producible optical chip, which hosts the sample and provides a waveguide for the illumination source, and a standard low-cost microscope to acquire super-resolved images via two different approaches. Waveguides composed of a material with high refractive-index contrast provide a strong evanescent field that is used for single-molecule switching and fluorescence excitation, thus enabling chip-based single-molecule localization microscopy. Additionally, multimode interference patterns induce spatial fluorescence intensity variations that enable fluctuation-based super-resolution imaging. As chip-based nanoscopy separates the illumination and detection light paths, total-internal-reflection fluorescence excitation is possible over a large field of view, with up to 0.5 mm × 0.5 mm being demonstrated. Using multicolour chip-based nanoscopy, we visualize fenestrations in liver sinusoidal endothelial cells. | en_US |
dc.description.sponsorship | The research leading to these results has received funding from the European Union's Seventh
Framework Programme (FP7/2007-2013) under grant agreement n° 336716 (B.S.A.). This work was also supported by the Research Council of Norway (grant no. 244764/F11 to B.S.A.), and the German Academic Exchange Service (grant no. 57160327 to M.S.). R.D. acknowledges additional support by grant no. KF2140610NT4 of the German Federal Ministry for Economic Affairs and Energy. | en_US |
dc.description | Accepted manuscript version. Published version available at <a href=http://doi.org/10.1038/nphoton.2017.55>http://doi.org/10.1038/nphoton.2017.55</a>. | en_US |
dc.identifier.citation | Diekmann, R., Helle, Ø.I., Øie, C.I., McCourt, P., Huser, T.R, Schüttpelz, M. & Ahluwalia, B.S. (2017). Chip-based wide field-of-view nanoscopy. <i>Nature Photonics, 11</i>, 322-328. http://doi.org/10.1038/nphoton.2017.55 | en_US |
dc.identifier.cristinID | FRIDAID 1482342 | |
dc.identifier.doi | 10.1038/nphoton.2017.55 | |
dc.identifier.issn | 1749-4885 | |
dc.identifier.issn | 1749-4893 | |
dc.identifier.uri | https://hdl.handle.net/10037/11998 | |
dc.language.iso | eng | en_US |
dc.publisher | Nature Publishing Group | en_US |
dc.relation.ispartof | Helle, Ø.I. (2019). On-chip optical nanoscopy: towards high throughput and multi-modality. (Doctoral thesis). <a href=https://hdl.handle.net/10037/16641>https://hdl.handle.net/10037/16641. </a> | |
dc.relation.journal | Nature Photonics | |
dc.relation.projectID | info:eu-repo/grantAgreement/EC/FP7/336716//// | en_US |
dc.relation.projectID | info:eu-repo/grantAgreement/RCN/FundingProgram/244764/F11/Norway/// | |
dc.rights.accessRights | openAccess | en_US |
dc.subject | Super-resolution microscopy | en_US |
dc.subject | Total internal reflection microscopy | en_US |
dc.title | Chip-based wide field-of-view nanoscopy | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |