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  Flow conditions in the vicinity of microstructured interfaces studied by holography and implications for the assembly of artificial actin networks

Weiße, S., Heydt, M., Maier, T., Schulz, S., Spatz, J. P., Grunze, M., et al. (2011). Flow conditions in the vicinity of microstructured interfaces studied by holography and implications for the assembly of artificial actin networks. Physical Chemistry Chemical Physics, 13(29), 13395-13402. doi:10.1039/C1CP20153K.

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 Urheber:
Weiße, Sebastian, Autor
Heydt, Matthias, Autor
Maier, Timo1, 2, Autor           
Schulz, Simon1, Autor           
Spatz, Joachim P.1, 2, Autor           
Grunze, Michael1, 2, Autor           
Haraszti, Tamas1, 2, Autor           
Rosenhahn, Axel, Autor
Affiliations:
1Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society, ou_2364731              
2Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany, ou_persistent22              

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 Zusammenfassung: Microstructured fluidic devices have successfully been used for the assembly of free standing actin networks as mechanical model systems on the top of micropillars. The assembly occurs spontaneously at the pillar heads when preformed filaments are injected into the channel. In order to reveal the driving mechanism of this localization, we studied the properties of the flow profile by holographic tracking. Despite the strong optical disturbances originating from the pillar field, 2 μm particles were traced with digital in-line holographic microscopy (DIHM). Trajectories in the pillar free region and local alterations of the flow profile induced by the channel structure in the pillar decorated region can be distinguished. Velocity histograms at different z-positions reveal that the laminar flow profile across the channel shows a difference between the minimum in the z-component of the velocity field and the maximum of the overall velocity. This minimum drag in vertical direction is present at the top of the pillars and explains why biopolymer networks readily assemble in this region instead of forming a homogeneous three-dimensional network in between the pillars. On the basis of the observations we propose a new mechanism for actin network formation on top of the microstructures.

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Sprache(n): eng - English
 Datum: 2011-01-182011-06-032011-06-232011
 Publikationsstatus: Erschienen
 Seiten: 8
 Ort, Verlag, Ausgabe: -
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 Art der Begutachtung: Expertenbegutachtung
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Titel: Physical Chemistry Chemical Physics
  Kurztitel : Phys. Chem. Chem. Phys.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, England : Royal Society of Chemistry
Seiten: - Band / Heft: 13 (29) Artikelnummer: - Start- / Endseite: 13395 - 13402 Identifikator: ISSN: 1463-9076
CoNE: https://pure.mpg.de/cone/journals/resource/954925272413_1