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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. doi:10.1101/2020.10.30.361808.

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2020.10.30.361808v1.full.pdf (Preprint), 5MB
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2020.10.30.361808v1.full.pdf
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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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Schlüßler, Raimund1, Autor
Kim, Kyoohyun1, 2, Autor           
Nötzel, Martin1, Autor
Taubenberger, Anna1, Autor
Abuhattum Hofemeier, Shada2, 3, Autor           
Beck, Timon2, Autor           
Müller, Paul2, 3, Autor           
Maharana, Shovamayee1, Autor
Cojoc, Gheorghe1, Autor
Girardo, Salvatore2, 3, Autor           
Hermann, Andreas4, Autor
Alberti, Simon4, Autor
Guck, Jochen1, 2, 3, Autor           
Affiliations:
1Technische Universität Dresden, ou_persistent22              
2Guck Division, Max Planck Institute for the Science of Light, Max Planck Society, ou_3164416              
3Max-Planck-Zentrum für Physik und Medizin, Max Planck Institute for the Science of Light, Max Planck Society, ou_3164414              
4external, ou_persistent22              

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 Zusammenfassung: 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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Sprache(n): eng - English
 Datum: 2020-10-30
 Publikationsstatus: Online veröffentlicht
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 Identifikatoren: DOI: 10.1101/2020.10.30.361808
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Titel: bioRxiv
Genre der Quelle: Kommentar
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