Evolution of DNA compaction in microchannels

被引:30
作者
Dootz, Rolf
Otten, Alexander
Koester, Sarah
Struth, Bernd
Pfohl, Thomas
机构
[1] Max Planck Inst Dynam & Self Org, D-37073 Gottingen, Germany
[2] Univ Ulm, Dept Appl Phys, D-89069 Ulm, Germany
[3] European Synchrotron Radiat Facil, F-38043 Grenoble, France
关键词
D O I
10.1088/0953-8984/18/18/S10
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
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.
引用
收藏
页码:S639 / S652
页数:14
相关论文
共 39 条
  • [1] Atkins P., 2014, Physical chemistry
  • [2] Physics and applications of microfluidics in biology
    Beebe, DJ
    Mensing, GA
    Walker, GM
    [J]. ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 : 261 - 286
  • [3] CONCENTRATION EVALUATION OF CHROMATIN IN UNSTAINED RESIN-EMBEDDED SECTIONS BY MEANS OF LOW-DOSE RATIO-CONTRAST IMAGING IN STEM
    BOHRMANN, B
    HAIDER, M
    KELLENBERGER, E
    [J]. ULTRAMICROSCOPY, 1993, 49 (1-4) : 235 - 251
  • [4] Structure/function relationships of polyamidoamine/DNA dendrimers as gene delivery vehicles
    Braun, CS
    Vetro, JA
    Tomalia, DA
    Koe, GS
    Koe, JG
    Middaugh, CR
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 94 (02) : 423 - 436
  • [5] Solvent mediated interactions in the structure of the nucleosome core particle at 1.9 Å resolution
    Davey, CA
    Sargent, DF
    Luger, K
    Maeder, AW
    Richmond, TJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2002, 319 (05) : 1097 - 1113
  • [6] Structural basis of polyamine-DNA recognition: spermidine and spermine interactions with genomic B-DNAs of different GC content probed by Raman spectroscopy
    Deng, H
    Bloomfield, VA
    Benevides, JM
    Thomas, GJ
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (17) : 3379 - 3385
  • [7] Deng H, 1999, BIOPOLYMERS, V50, P656, DOI 10.1002/(SICI)1097-0282(199911)50:6<656::AID-BIP10>3.0.CO
  • [8] 2-9
  • [9] DENNIG J, 2002, REV MOL BIOTECHNOL, V90, P339, DOI DOI 10.1016/S1389-0352(01)00066-6
  • [10] DURAND D, 1992, J PHYS II, V2, P1769, DOI 10.1051/jp2:1992233