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  Combined fluorescence, optical diffraction tomography and Brillouin microscopy

Schlüßler, R., Kim, K., Nötzel, M., Taubenberger, A., Abuhattum Hofemeier, S., Beck, T., et al. (2020). Combined fluorescence, optical diffraction tomography and Brillouin microscopy. bioRxiv 2020.10.30.361808.

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2020.10.30.361808v1.full.pdf (Preprint), 5MB
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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.

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 Creators:
Schlüßler, Raimund1, Author
Kim, Kyoohyun1, 2, Author           
Nötzel, Martin1, Author
Taubenberger, Anna1, Author
Abuhattum Hofemeier, Shada2, 3, Author           
Beck, Timon2, Author           
Müller, Paul2, 3, Author           
Maharana, Shovamayee1, Author
Cojoc, Gheorghe1, Author
Girardo, Salvatore2, 3, Author           
Hermann, Andreas4, Author
Alberti, Simon4, Author
Guck, Jochen1, 2, 3, Author           
Affiliations:
1Technische Universität Dresden, ou_persistent22              
2Guck Division, Max Planck Institute for the Science of Light, Max Planck Society, ou_3164416              
3Guck Division, Max-Planck-Zentrum für Physik und Medizin, Max Planck Institute for the Science of Light, Max Planck Society, ou_3596668              
4external, ou_persistent22              

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 Abstract: Quantitative measurements of physical parameters become increasingly important for understanding biological processes. Brillouin microscopy (BM) has recently emerged as one technique providing the 3D distribution of viscoelastic properties inside biological samples — so far relying on the implicit assumption that refractive index (RI) and density can be neglected. Here, we present a novel method (FOB microscopy) combining BM with optical diffraction tomography and epi-fluorescence imaging for explicitly measuring the Brillouin shift, RI and absolute density with molecular specificity. We show that neglecting the RI and density might lead to erroneous conclusions. Investigating the cell nucleus, we find that it has lower density but higher longitudinal modulus. Thus, the longitudinal modulus is not merely sensitive to the water content of the sample — a postulate vividly discussed in the field. We demonstrate the further utility of FOB on various biological systems including adipocytes and intracellular membraneless compartments. FOB microscopy can provide unexpected scientific discoveries and shed quantitative light on processes such as phase separation and transition inside living cells.

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Language(s): eng - English
 Dates: 2020-10-30
 Publication Status: Published online
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 Identifiers: bioRxiv: 10.1101/2020.10.30.361808
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Title: bioRxiv 2020.10.30.361808
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