Author:
Marthy Baptiste,Bénéfice Maëlle,Baffou Guillaume
Abstract
AbstractThe article introduces an optical microscopy technique capable of simultaneously acquiring quantitative fluorescence and phase (or equivalently wavefront) images with a single camera sensor, avoiding any delay between both images, or registration of images acquired separately. The method is based on the use of a 2-dimensional diffraction grating (aka cross-grating) positioned at a millimeter distance from a 2-color camera. Fluorescence and wavefront images are extracted from the two color channels of the camera, and retrieved by image demodulation. The applicability of the method is illustrated on various samples, namely fluorescent micro-beads, bacteria and mammalian cells.
Funder
Horizon 2020 Framework Programme
HORIZON EUROPE Framework Programme
Publisher
Springer Science and Business Media LLC
Reference37 articles.
1. Cox, G. Fundamentals of Fluorescence Microscopy (Jenny Stanford Publishing, 2019).
2. Valeur, B. Molecular Fluorescence: Principles and Applications (Wiley-VCH, 2007).
3. Lakovicz, J. R. Principles of Fluorescence Spectroscopy (Springer, 2007).
4. Montecinos-Franjola, F., Bauer, B. L., Mears, J. A. & Ramachandran, R. GFP fluorescence tagging alters dynamin-related protein 1 oligomerization dynamics and creates disassembly-refractory puncta to mediate mitochondrial fission. Sci. Rep. 10, 14777 (2020).
5. Baffou, G., Rigneault, H., Marguet, D. & Jullien, L. A critique of methods for temperature imaging in single cells. Nat. Methods 11, 899–901 (2014).
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