Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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