Carmel L Howe
Surface plasmon resonance imaging of excitable cells
Howe, Carmel L; Webb, Kevin F; Abayzeed, Sidahmed A; Anderson, David J; Denning, Chris; Russell, Noah A
Authors
Dr KEVIN WEBB KEVIN.WEBB@NOTTINGHAM.AC.UK
ASSOCIATE PROFESSOR
Dr SIDAHMED ABAYZEED SIDAHMED.ABAYZEED2@NOTTINGHAM.AC.UK
ASSISTANT PROFESSOR
David J Anderson
Professor CHRIS DENNING chris.denning@nottingham.ac.uk
PROFESSOR OF STEM CELL BIOLOGY
Noah A Russell
Abstract
Surface plasmons (SPs) are surface charge density oscillations occuring at a metal/dieletric interface and are highly sensitive to refractive index variations adjacent to the surface. This sensitivity has been exploited successfully for chemical and biological assays. In these systems, a surface plasmon resonance (SPR)-based sensor detects temporal variations in the refractive index at a point. SPR has also been used in imaging systems where the spatial variations of refractive index in the sample provide the contrast mechanism. SPR imaging systems using high numerical aperture (NA) objective lenses have been designed to image adherent live cells with high magnification and near-diffraction limited spatial resolution. Addressing research questions in cell physiology and pharmacology often requires the development of a multimodal microscope where complementary information can be obtained.
In this paper, we present the development of a multimodal microscope that combines SPR imaging with a number of additional imaging modalities including bright-field, epifluorescence, total internal reflection microscopy and SPR fluorescence microscopy. We used a high NA objective lens for SPR and TIR microscopy and the platform has been used to image live cell cultures demonstrating both fluorescent and label-free techniques. Both the SPR and TIR imaging systems feature a wide field of view (~300 µm) that allows measurements from multiple cells whilst maintaining a resolution sufficient to image fine cellular processes. The capability of the platform to perform label-free functional imaging of living cells was demonstrated by imaging the spatial variations in contractions from stem cell-derived cardiomyocytes. This technique shows promise for non-invasive imaging of cultured cells over very long periods of time during development.
Citation
Howe, C. L., Webb, K. F., Abayzeed, S. A., Anderson, D. J., Denning, C., & Russell, N. A. (2019). Surface plasmon resonance imaging of excitable cells. Journal of Physics D: Applied Physics, 52(10), Article 104001. https://doi.org/10.1088/1361-6463/aaf849
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 12, 2018 |
Online Publication Date | Jan 4, 2019 |
Publication Date | Mar 6, 2019 |
Deposit Date | Jan 7, 2019 |
Publicly Available Date | Jan 7, 2019 |
Journal | Journal of Physics D: Applied Physics |
Print ISSN | 0022-3727 |
Electronic ISSN | 1361-6463 |
Publisher | IOP Publishing |
Peer Reviewed | Peer Reviewed |
Volume | 52 |
Issue | 10 |
Article Number | 104001 |
DOI | https://doi.org/10.1088/1361-6463/aaf849 |
Keywords | Acoustics and Ultrasonics; Electronic, Optical and Magnetic Materials; Surfaces, Coatings and Films; Condensed Matter Physics |
Public URL | https://nottingham-repository.worktribe.com/output/1447131 |
Publisher URL | https://iopscience.iop.org/article/10.1088/1361-6463/aaf849 |
Additional Information | Journal title: Journal of Physics D: Applied Physics; Article type: paper; Article title: Surface plasmon resonance imaging of excitable cells; Copyright information: © 2019 IOP Publishing Ltd; License information: cc-by Original content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence. Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI.; Date received: 2018-08-07; Date accepted: 2018-12-12; Online publication date: 2019-01-04 |
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Publisher Licence URL
https://creativecommons.org/licenses/by/3.0/
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