Evolution of DNA compaction in microchannels

2006-04-19 | journal article; research paper. A publication with affiliation to the University of Göttingen.

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​Evolution of DNA compaction in microchannels​
Dootz, R.; Otten, A.; Köster, S. ; Struth, B. & Pfohl, T.​ (2006) 
Journal of Physics: Condensed Matter18(18) pp. 639​-652​.​ DOI: https://doi.org/10.1088/0953-8984/18/18/s10 

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Authors
Dootz, Rolf; Otten, Alexander; Köster, Sarah ; Struth, Bernd; Pfohl, Thomas
Abstract
Combining microfluidics with x-ray microdiffraction and Raman microscopy, the dynamic behaviour of soft matter, with specific consideration of the molecular structure, can be investigated. Microfluidic systems enable a reduction of sample volume and shorter reaction times. By performing experiments under continuous microflow, material damage is avoided and the influence of external stress on biomacromolecules can be analysed. The generated elongated flow induces alignment of the investigated materials, allowing for an improved structural characterization. Here, the dynamics of the compaction of DNA by polypropyleneimine dotriacontaamine dendrimers, generation 4 is studied. As a consequence of the laminar flow inside the microchannels, highly defined, diffusion-controlled compaction of the DNA occurs enabling the study of different states of the reaction during one measurement by varying the observation position in the channels. The evolution of a columnar mesophase with an in-plane square symmetry is monitored by x-ray microdiffraction and the molecular interaction between the two reactants is traced using Raman microscopy, leading to a more profound comprehension of the condensation reaction. The experimental results are in accordance with finite element method simulations of the flow and diffusion profiles in the elongated flow device.
Issue Date
19-April-2006
Journal
Journal of Physics: Condensed Matter 
Organization
Institut für Röntgenphysik 
Working Group
RG Köster (Cellular Biophysics) 
ISSN
0953-8984
Language
English
Subject(s)
x-ray scattering; molecular biophysics; microfluidics

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