Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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Arbeitskreis Biologische Physik Freitag<br />
tified by statistically distributed or alternating gold and silver islands. A<br />
microscope with ATR capability allows to evaluated both, the coordinate<br />
system and the diffusion of molecular probes in cells.<br />
AKB 50.34 Fr 10:30 B<br />
Elastic interactions of cells with soft materials — •Ilka Bischofs<br />
and Ulrich Schwarz — Max Planck Institut für Kolloid- und Grenzflächenforschung,<br />
Theorie, 14424 Potsdam<br />
Mechanically active cells sense the mechanical properties of their environment<br />
and respond by strenghtening their cytoskeleton in the direction<br />
of maximal effective stiffness. Rigidity gradients, prestrain induced<br />
by external forces, traction by other cells, and the presence of sample<br />
boundaries locally alter the effective stiffness encountered by contractile<br />
cells. We model cells as anisotropic force contraction dipoles and use linear<br />
elasticity theory to calculate optimal cell organization in soft media.<br />
Our predictions for single cells agree nicely with experiments for fibroblasts:<br />
cells orient toward clamped and away from free surfaces and along<br />
the direction of tensile strain. The elastic interaction between cells shows<br />
a similar angular dependence as electrical dipoles. At low cell density,<br />
this leads to strings of cells, while at high cell density, branching into<br />
ring-like structures occurs.<br />
AKB 50.35 Fr 10:30 B<br />
Active forces of motile cells — •Claudia Brunner, Michael<br />
Gögler, Allen Ehrlicher, and Josef Käs — a<br />
Cellular motility is a ubiquitous component of prokaryotic and eukaryotic<br />
cells, spanning varied functions from the immune system, to the<br />
developing brain, to the grave invasiveness of cancer.<br />
Various individual components, such as molecular motors and actin<br />
filament polymerization have been explored to explain cell movement,<br />
but the cell as a whole system is not well understood. Experiments on<br />
living cells are necessary to understand the properties and abilities of<br />
their polymer networks functioning together as one system.<br />
The atomic force microscope is an excellent tool to determine the<br />
mechanical forces which are responsible for cell movement. With a<br />
polystyrene bead glued on a commercial AFM-tip, living cells can be<br />
safely measured. We have probed fast moving keratocytes and directly<br />
measured the cell extension forces, allowing us to compare extension<br />
forces with the cells velocities and other properties.<br />
AKB 50.36 Fr 10:30 B<br />
Functionalization and Passivation of a Silicon-on-Insulator<br />
based Sensor Device — •Petra A. Neff, Michael G. Nikolaides,<br />
Stefan Rauschenbach, Simon Q. Lud, and Andreas<br />
R. Bausch — Lehrstuhl für Biophysik - E22, Technische Universität<br />
München, 85747 Garching<br />
The sensitive and specific detection of biomolecular interactions relies<br />
on the functionalization and passivation of the detecting surfaces.<br />
Recently, a new Silicon-on-Insulator (SOI) based thin film resistor device<br />
for chemical and biological sensor applications was introduced. It<br />
has been shown that this sensor is highly sensitive to variations of the<br />
surface potential evoked by the adsorption of small amounts of charged<br />
molecules. Whereas most of the conventional detection techniques require<br />
the labeling of molecules, the SOI based sensor allows a label-free<br />
detection of interactions.<br />
Here we discuss the passivation and functionalization of the bare silicon<br />
oxide surface by physical adsorption of polyelectrolytes and the covalent<br />
binding of silanes. Results of the adsorption of PAH/PSS multilayers are<br />
presented and their interpretation will be discussed. First results of the<br />
application of the sensor device towards the label-free detection of DNA<br />
hybridization will be presented.<br />
AKB 50.37 Fr 10:30 B<br />
Activation of Integrin Function by Nanopatterned Adhesive Interfaces<br />
— •Marco Arnold 1 , Elisabetta Ada Cavalcanti 1 ,<br />
Roman Glass 1 , Jacques Blümmel 1 , Wolfgang Eck 2 , Martin<br />
Kantlehner 3 , Horst Kessler 3 , and Joachim P. Spatz 1<br />
— 1 University of Heidelberg, Institute for Physical Chemistry, Biophysical<br />
Chemistry, INF 253, D-69120 Heidelberg — 2 University of Heidelberg,<br />
Institute for Physical Chemistry, Applied Physical Chemistry, INF<br />
253, D-69120 Heidelberg — 3 Technical University of Munich, Institute<br />
for Organic Chemistry and Biochemistry, Lichtenbergstrasse 4, D-85747<br />
Garching<br />
To study the function behind molecular arrangement of single integrins<br />
in cell adhesion, we designed a hexagonally closepacked rigid template of<br />
cell adhesive gold nanodots by lithographic means of diblock copolymer<br />
selfassembly. The diameter of the adhesive dots are smaller than 8nm,<br />
which allows the binding of one integrin per dot. These dots are positioned<br />
with high precision at 28, 58, 73 and 85nm spacing at interfaces.<br />
A separation of more than 73nm between the dots results in limited cell<br />
attachment and spreading and reduces the formation of focal adhesion<br />
and actin stress fibers. We attribute these cellular responses to restricted<br />
integrin clustering rather than insufficient number of ligand molecules<br />
in cellmatrix interface since micronanopatterned substrates consisting of<br />
alternating fields with dense and no nanodots support cell adhesion. We<br />
propose that the range between 58 and 73nm is a universal length scale<br />
for integrin clustering and activation.<br />
AKB 50.38 Fr 10:30 B<br />
Coherent Scatter Computed Tomography — •Johannes Delfs 1 ,<br />
Jens-Peter Schlomka 1 , and Robert L. Johnson 2 — 1 Philips Research<br />
Laboratories Hamburg, Röntgenstrasse 24-26, 22335 Hamburg,<br />
Germany — 2 Institut für Experimentalphysik, Universität Hamburg, Luruper<br />
Chaussee 149, 22761 Hamburg, Germany<br />
The dominant component of low-angle scatter in the energy regime<br />
of diagnostic radiology ( 60 keV) is coherent scatter. This leads to the<br />
phenomenon of x-ray diffraction, which is widely used for determining<br />
atomic structure in material science.<br />
A reconstructive tomographic imaging technique (”Coherent Scatter<br />
Computed Tomography (CSCT) ”) is presented for the spatially-resolved<br />
measurement of the coherent scatter cross-section in extended objects.<br />
These diffraction patterns supplement conventional CT images in material<br />
discrimination.The technique is based on the energy analysis, at<br />
known angle, of coherent x-ray scatter by polychromatic radiation employing<br />
a novel energy-resolving CdZnTe detector array. Images of test<br />
objects are shown to illustrate the feasibility of the technique and potential<br />
applications in medicine and industrial material inspection.<br />
AKB 50.39 Fr 10:30 B<br />
An individual-based Model to Tumor Growth in Vitro —<br />
•Drasdo Dirk 1 and Hoehme Stefan 2 — 1 MPI fuer Mathematik in<br />
den Naturwissenschaften, Inselstr. 22-26,Leipzig — 2 Interdisciplinary<br />
Inst. for Bioinformatics, Kreuzstr. 7b, Leipzig<br />
We present a mathematical model to study the spatio-temporal growth<br />
dynamics of two-dimensional tumor monolayers and three-dimensional<br />
tumor spheroids as a complementary tool to in-vitro experiments. Within<br />
our model each cell is represented as an individual object and parameterized<br />
by cell-biophysical and cell-kinetic parameters that can all be experimentally<br />
determined. Hence our modeling strategy in principle provides<br />
a link between mechanisms on the microscopic level of individual cells<br />
and the macroscopic properties of a growing tumor. We find a remarkable<br />
robustness of the growth kinetics and patterns in early growth stages<br />
although their mechanistic origin can be different. Quantitative comparisons<br />
of computer simulations with our model to published experimental<br />
observations on monolayer cultures suggest a biomechanically-mediated<br />
form of growth inhibition during the experimentally observed transition<br />
from exponential to sub-exponential growth at sufficiently large tumor<br />
sizes. Our simulations show that for avascular tumor spheroids this transition<br />
can usually be explained by a nutrient or oxygen depletion, and<br />
predict that it becomes biomechanically triggered at a sufficiently large<br />
nutrient and oxygen supply.<br />
AKB 50.40 Fr 10:30 B<br />
Dynamics of Tension in Semiflexible Polymers — •Oskar Hallatschek<br />
1 , Erwin Frey 1,2 , and Klaus Kroy 1 — 1 Abteilung Theorie,<br />
Hahn-Meitner Institut, Glienicker Str. 100, 14109 Berlin, Germany<br />
— 2 Fachbereich Physik, Freie Universität,14195 Berlin, Germany<br />
We present a general discussion of non-equilibrium tension propagation<br />
through a semiflexible polymer in various situations of experimental<br />
interest. Typical situations include the response of the polymer’s conformation<br />
to a given longitudinal force at one end, or the relaxation of the<br />
polymer after it has been equilibrated under a certain applied tension.<br />
In both cases the propagation of tension exhibits power law behavior,<br />
but with distinct dynamic exponents. Whereas the initial exponent always<br />
equals 1/8, the exponent for late time propagation depends on the<br />
experimental situation. Based on a set of coarse-grained equations of motion<br />
we give a unified theoretical explanation of the various scenarios. In<br />
addition, we discuss the behavior of end grafted chains in an external<br />
field, and analyze the problem of a polymer that undergoes a sudden<br />
temperature change.