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Plenarvorträge - DPG-Tagungen

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Arbeitskreis Biologische Physik Freitag<br />

AKB 50.101 Fr 10:30 B<br />

Biomechanical investigations of collagen fibrils — •Stefan<br />

Strasser, Wolfgang M. Heckl, and Stefan Thalhammer —<br />

Department for Geo und Environmental Sciences, GeoBioCenter and<br />

Center for Nanoscience, Ludwig Maximilians University, Theresienstr.<br />

41, 80333 Munich, Germany<br />

Collagen fibrils, type I and II with various periodicities were investigated,<br />

using the Atomic Force Microscope both as tool for imaging and<br />

nanomanipulation. Native and fibrous long spacing (FLS) collagen fibrils<br />

were formed by self assembling in vitro, using a special setup for<br />

dialysing. Depending on the conditions of assembly, collagen may form a<br />

variety of different structures. The received collagen fibrils of type I had<br />

a bending pattern of 67nm for the native fibrils, and 200nm to 300nm<br />

for the FLS fibrils. Collagen is a system which shows a large degree of<br />

polymorphism. All fibrils with a periodicity greater than 67nm can be<br />

considered as FLS collagen. The collagen fibrils were imaged in air and<br />

in liquids. To determine the elastic properties of collagen fibrils the tip of<br />

the AFM was used as a nano-indentor. Force displacement curves were<br />

recorded in liquids at different hights of collagen clusters as well as on<br />

single fibrils and the youngs modulus has been calculated utilizing the<br />

Hertzian theory. Results will be shown and discussed on single fibrils and<br />

on multilayer stacks.<br />

AKB 50.102 Fr 10:30 B<br />

Contact Resistance of Cell Silicon Junctions Measured with<br />

Voltage-Sensitive Dye — •Raimund Gleixner and Peter<br />

Fromherz — MPI für Biochemie, Abt. Membran und Neurophysik,<br />

Martinsried<br />

The electrical sheet resistance between a cell and a solid substrate is<br />

a crucial parameter for bioelectronic coupling. It can be determined by<br />

applying transient voltages to a silicon chip, observing the response of<br />

the membrane with a voltage-sensitive dye (Braun:PRL86,2905,2002).<br />

We used the novel dye ANNINE-5 (Hübener:JPC,107,7896,2003) to<br />

study the contact between HEK293 cells and fibronectin-coated oxidized<br />

silicon. We determined the sheet resistance as a function of salt concentration<br />

in the bath. A train of voltage transients was applied to the<br />

chip and the fluorescence in the attached membrane was averaged in a<br />

confocal microscope over several periods. For sinusoidal stimulation, the<br />

frequency dependent spatially resolved transfer function was fitted with<br />

a core-coat conductor model of the junction.<br />

We found that the sheet resistance was proportional to the bulk specific<br />

resistance. This indicated a cleft of 80nm filled with bulk electrolyte.<br />

¿From fluorescence interference contrast (FLIC)microscopy we obtained<br />

a distance of 70nm between membrane and chip, independent of salt<br />

concentration. We conclude: (i)The narrow extracellular space of cell<br />

adhesion is filled with bulk electrolyte. (ii)The sheet resistance can be<br />

enhanced by enhancing the resistance of the bath.<br />

AKB 50.103 Fr 10:30 B<br />

Correlation functions and Boltzmann Langevin approach for<br />

driven one dimensional lattices gases — •Paolo Pierobon 1,2 , Felix<br />

Von Oppen 2 , Andrea Parmeggiani 1 , and Erwin Frey 1,2 for the<br />

collaboration — 1 Hahn-Meitner Institut, Abteilung Theorie, Glienicker<br />

Str.100, D-14109 Berlin, Germany — 2 Fachbereich Physik, Freie Universitaet<br />

Berlin, Arnimallee 14, D-14195 Berlin, Germany<br />

The Totally Asymmetric Simple Exclusion Process (TASEP) is a simple<br />

one dimensional driven lattice gas model. It may serve as a simplified<br />

model highlighting some aspects of traffic flow and biological transport<br />

phenomena, e.g. motion of molecular motors on microtubules. At the<br />

same time it has become a paradigm of non-equilibrium systems which<br />

exhibit dynamic phase transitions driven by the boundaries. Although<br />

the stationary density profile has been understood for long time, the time<br />

dependent properties are still under investigation. We study the dynamic<br />

correlation function of the particle density in such a system using real<br />

time Monte Carlo simulations. In certain regimes the results can be rationalized<br />

using a Boltzmann-Langevin approach i.e. adding a fluctuating<br />

current to the mean field equation in a phenomenological way. We also<br />

analyze our results within the ”domain wall”picture, where a “shock”<br />

separates two phases and fluctuates as a Brownian walker with reflective<br />

boundary conditions. Critical exponents are measured with great accuracy<br />

from the properties of autocorrelation function at the critical point<br />

(where three phases coexist), and in the maximal current phase. The<br />

results corroborate that the system, in such conditions, belongs to the<br />

KPZ universality class.<br />

AKB 50.104 Fr 10:30 B<br />

An off-lattice model for multicellular tumor spheroid growth —<br />

•Gernot Schaller and Michael Meyer-Hermann — Institut für<br />

Theoretische Physik, Zellescher Weg 17, 01062 Dresden<br />

We model three-dimensional multicellular tumor spheroids using an<br />

agent-based Delaunay/Voronoi-model which relies on experimentally accesible<br />

cellular properties.<br />

For the detection of natural neighbors we use three-dimensional<br />

weighted dynamic and kinetic Delaunay/Voronoi tessellations. The<br />

resulting bidirectional graph can be dynamically updated with in<br />

average linear complexity versus the number of cells. Cells are assumed<br />

to be elastically deformable spheres with varying radii. The growth of<br />

cells is modeled by coupling the cells to a reaction-diffusion-equation for<br />

nutrients. The dynamics is then calculated using the Langevin equation<br />

in the overdamped limit.<br />

We study the emergence of typical avascular tumor morphologies starting<br />

with a single tumor cell. The influence of several mechanisms such<br />

as nutrient limitation, external tissue pressure and intercellular adhesion<br />

on growth and morphology is studied.<br />

This work has been financially supported by the SMWK.<br />

AKB 50.105 Fr 10:30 B<br />

Molecular dynamics of intramyocellular metabolites from highresolution<br />

in vivo 1 H NMR spectroscopy — •Leif Schröder 1 ,<br />

Christian Schmitz 2 , and Peter Bachert 1 — 1 Dept. of Medical<br />

Physics in Radiology, Deutsches Krebsforschungszentrum, Heidelberg,<br />

Germany — 2 Biophysikalische Chemie, Physikalisch-Chemisches Institut,<br />

Universität Heidelberg, Germany<br />

Residual dipolar couplings affecting resonances in 1 H NMR spectra of<br />

living tissue have been discovered 10 years ago (Kreis et. al.). Our purpose<br />

was to explore molecular dynamics of creatine (Cr), taurine (Tau),<br />

and carnosine (Cs) in human calf muscle (m. gastrocnemius) in vivo by<br />

analyzing dipolar-coupled multiplets in localized high-resolution 1 H NMR<br />

spectra (STEAM and PRESS technique). Measurements were performed<br />

in healthy volunteers on a whole-body MR tomograph at B0 = 1.5T. The<br />

residual coupling strength SD0 derived from the spectra was compared<br />

to the coupling constant D0 calculated using the internuclear distance<br />

under the assumption of completely frozen molecular libration. The order<br />

parameter S is a measure of molecular mobility. We found a large<br />

S (1.2 × 10 −2 ) for the detectable Cs spin system, i.e. the imidazole ring<br />

protons, which indicates restricted reorientational motion of this compound<br />

in contrast to high mobilities of the CH2 and CH3 groups of Tau<br />

and Cr (S = 1.4 − 3 × 10 −4 ). The observed motional restriction of Cs is<br />

explained by interaction of the metabolite with phospholipids in muscle<br />

cell membranes. These results demonstrate that 1 H NMR spectroscopy<br />

permits noninvasive studies of intermolecular processes in vivo.<br />

AKB 50.106 Fr 10:30 B<br />

Are there lipid rafts? — •Heiko Heerklotz — Biozentrum Basel,<br />

Klingelbergstr. 70, CH-4056 Basel<br />

Functional domains in biological membranes and the role of lipids in<br />

the formation of such structures are still not unequivocally clarified. A<br />

classical definition of the term lipid rafts refers to large, long-lived domains<br />

in native cellular membranes that are formed by a spontaneous demixing<br />

of a liquid ordered phase rich in sphingomyelin (SM) and cholesterol<br />

(Cho) from the fluid, phosphatidylcholine (PC)-rich matrix. Rafts<br />

have been believed to accumulate large numbers of proteins and it has<br />

been assumed that rafts can be isolated from membranes as so-called detergent<br />

resistant membrane fragments (DRMs). Our investigations have<br />

revealed however that these common assumptions are inconsistent. Putative<br />

lipid rafts having stability properties similar to liquid ordered domains<br />

in a PC-SM-Cho mixture cannot be isolated by detergent without<br />

changing their properties substantially. We came to this conclusion on<br />

the basis of studies of the stability of domains and intermolecular interactions<br />

between lipids (POPC-SM-Cho) and detergents (Triton X-100<br />

and others) by various microcalorimetric techniques (isothermal titration<br />

calorimetry, differential scanning calorimetry, pressure perturbation<br />

calorimetry) and solid-state NMR. A simple thermodynamic model based<br />

on the enthalpy and entropy of the interactions of different lipids with<br />

the detergent explains the phenomena.<br />

AKB 50.107 Fr 10:30 B<br />

Contact mechanics of bioinspired fibrillar structures — •Ralph<br />

Spolenak, Stanislav Gorb, and Eduard Arzt — Max-Planck-<br />

Institut für Metallforschung, Heisenbergstr. 3, D- 70569 Stuttgart

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