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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.

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