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Plenarvorträge - DPG-Tagungen

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Arbeitskreis Biologische Physik Freitag<br />

und gemessen werden, die als Modellverbindungen für den Einsatz dieser<br />

Sonde in den ” Life Sciences“ dienen werden. Im Vergleich zu anderen<br />

TDPAC-Isotopen verfügt diese Sonde über eine sehr lange Lebensdauer<br />

des Zwischenzustandes (tN = 382 ns) und damit über eine exzellente Frequenzauflösung,<br />

die sie für Dynamik-Studien prädestinieren. Die 204m Pb-<br />

Aktiviät wurde auch mit einem 204 Bi/ 204m Pb-Generator hergestellt. Mit<br />

dieser Sonde sind zum ersten Mal TDPAC-Experimente mit einem Isomer<br />

im ” Heimlabor“ möglich. Die Ergebnisse der 204m Pb-TDPAC-Messungen<br />

am ISOLDE/CERN und an der Uni Leipzig werden vorgestellt.<br />

AKB 50.27 Fr 10:30 B<br />

A model for pathfinding and targeting in mixed populations<br />

of axons — •Peter Borowski and Martin Zapotocky — Max-<br />

Planck-Institut für Physik komplexer Systeme; Nöthnitzer Str. 38; 01187<br />

Dresden<br />

We present a model for the development of a neural map involving<br />

multiple axon species. The model is motivated by the neural connectivity<br />

scheme of the olfactory system, where axons start in a spatially disordered<br />

configuration in the sensory epithelium, yet converge to specific<br />

points on the olfactory bulb depending on which type of odorant receptor<br />

they express. An important ingredient of our model is the presence<br />

of axon-axon interactions which lead to preferential bundling of axons of<br />

the same species. We classify the connectivity patterns that develop in<br />

such a system in the presence and absence of spatially graded guidance<br />

cues, and discuss the robustness of the corresponding neural maps.<br />

AKB 50.28 Fr 10:30 B<br />

Minkowski Functionals of high-dimensional data sets: application<br />

to protein analysis — •Boris Breidenbach 1,2 , Hubert<br />

Mantz 1 , and Klaus Mecke 1,2 — 1 MPI für Metallforschung, Heisenbergstr.3,<br />

70569 Stuttgart — 2 Universität Stuttgart, Institut für theoretische<br />

und angewandte Physik, Pfaffenwaldring 57, 70569 Stuttgart<br />

The Minkowski functionals are a well established tool for the analysis<br />

of various types of spatial experimental data such as tomographic images<br />

of porous materials and atomic force measurements of thin polymer<br />

films where they have proven their ability to extract physically relevant<br />

information. Here, we present the first application of integral geometry in<br />

spaces with more than three dimensions: data is taken from microarray<br />

experiments of gene expression profiles in cells. Each protein is assigned<br />

a point in the high-dimensional concentration space. The functionals can<br />

be calculated exactly and efficiently for such decorated point distributions.<br />

The method is fast and statistically robust. We illustrate it by<br />

analyzing the gene-expression timecourse during the development of the<br />

Drosophila life cycle with respect to its clustering behaviour, i.e., its<br />

protein-protein interactions. The results are subsequently compared to<br />

standard techniques in bioinformatics such as hierarchical clustering and<br />

self-organising maps.<br />

AKB 50.29 Fr 10:30 B<br />

Filament depolimerization by motor molecules — •Gernot<br />

Klein 1 , Giovanni Cuniberti 2 , Karsten Kruse 1 , and Frank<br />

Jülicher 1 — 1 Max-Planck-Institut fuer Physik komplexer Systeme,<br />

Dresden — 2 Universitaet Regensburg, Regensburg<br />

Motor proteins are specialized molecules which bind to filaments of the<br />

cytoskeleton and are able to generate forces. An unusual protein, closely<br />

related to kinesin motors is MCAK, which binds to microtubule ends and<br />

depolymerizes them (1),(2).<br />

We study the process of MCAK binding to microtubules and subsequent<br />

depolymerization using stochastic models.Computer simulations<br />

of a one-dimensional hopping model are compared to the mean-field theory<br />

of the adopted discrete model.Our theory can explain how molecules<br />

accumulate at depolymerizing ends.<br />

(1) A.W. Hunter, M.Caplow, D.L. Coy, W.O. Hancock, S. Diez,<br />

L.Wordeman, J. Howard; Mol. Cell, Vol 11, 445-457, 2003.<br />

(2) R. Ohi, M.L. Coughlin, W.S. Lane, T. Mitchison; Dev. Cell, Vol.5,<br />

309-321, 2003.<br />

AKB 50.30 Fr 10:30 B<br />

In-situ investigation of wood pyrolysis with synchrotron radiation<br />

— •Gerald Andreas Zickler 1 , Cordt Zollfrank 2 , Manfred<br />

Burghammer 3 , and Oskar Paris 1 — 1 Max Planck Institute<br />

of Colloids and Interfaces, Dept. Biomaterials, Am Mühlenberg 1, D-<br />

14476 Potsdam, Germany — 2 Friedrich Alexander University Erlangen-<br />

Nuremberg, Dept. Materials Science - Glass and Ceramics, Martensstr.<br />

5, D-91058 Erlangen, Germany — 3 European Synchrotron Radiation Facility<br />

(ESRF), 6 Rue Jules Horowitz, F-38043 Grenoble, France<br />

Advanced cellular ceramics from biologically derived pre-forms have<br />

gained considerable interest over the last years. Aim of biomimetic materials<br />

synthesis is the transformation of biological tissue into anorganic<br />

structures for the production of biomorphous ceramics and composite<br />

materials with advanced properties. The present study is focusing on<br />

structural aspects of non oxidising pyrolysis of native spruce wood, with<br />

the aim to transform the hierarchical structure of wood into oriented Biocarbon.<br />

Microfocus synchrotron radiation is used in combination with a<br />

custom made furnace to study wood pyrolysis in situ. Scanning the specimens<br />

provides further information on the micrometre scale. Detailed<br />

time resolved diffraction data from single wood slices give deeper insight<br />

into the kinetics of cellulose degradation, nano pore formation and development<br />

of turbostratic carbon at different pyrolysis temperatures. The<br />

results are presented and discussed with respect to existing structural<br />

models of cellulose degradation from literature.<br />

AKB 50.31 Fr 10:30 B<br />

Modelling of Rhodopsin Chromophore — •Minoru Sugihara 1 ,<br />

Ana-Nicoleta Bondar 2 , Peter Entel 1 , Volker Buss 3 , and Marcus<br />

Elstner 4 — 1 Institute of Physics, University of Duisburg-Essen —<br />

2 IWR, University of Heidelberg — 3 Institute of Chemistry, University of<br />

Duisburg-Essen — 4 Institute of Physics, University of Paderborn<br />

Bovine retinal photoreceptor rhodopsin is the only one visual pigment<br />

whose three-dimensional atomic coordinates are available now [1,2]. It<br />

is composed of the 40-kDa apoprotein opsin (348 amino acids) and its<br />

chromophore. The chromophore of rhodopsin is 11-it cis-retinal which<br />

is covalently attached to Lys296 via a Schiff base. The Schiff base nitrogen<br />

atom is protonated and there is a salt-bridge between the protonated<br />

Schiff base and its counterion, Glu113. Illumination of light of ∼<br />

500nm leads to photoisomerization from 11-cis retinal to all-trans within<br />

200fs, which is the primary event in visual system and is the only lightdependent<br />

step. This is followed by a conformational change in the protein<br />

and after a series of intermediates, the pigment reaches the signaling<br />

state, the so-called meta-II. In the present work we focus on the modelling<br />

of the chromophore in the dark state (rhodopsin state) and the<br />

first intermediate state (batho state) based on the crystal structure of<br />

rhodopsin state [2]. We use the recently developed quantum mechanical<br />

/ molecular mechanical (QM/MM) method [3]. [1] K. Palczewski, et al.<br />

Science 2000, 289, 739. [2] T. Okada, et al. Proc. Natl. Acad. Sci, U.S.A.<br />

2002, 99, 5982. [3] Q. Cui, et al. J. Phys. Chem. B 2001, 20, 569.<br />

AKB 50.32 Fr 10:30 B<br />

Unbinding Transitions of Filament Bundles — •Jan Kierfeld,<br />

Torsten Kühne, and Reinhard Lipowsky — MPI für Kolloid- und<br />

Grenzflächenforschung, 14424 Potsdam<br />

Filament bundles are an important structural element of the cytoskeleton.<br />

We study the unbinding transition bundles of semiflexible filaments<br />

such as F-actin. The interaction between the filaments is mediated by<br />

crosslinking stickers. It is shown that the formation of a filament bundle<br />

requires a threshold concentration of stickers. We find that the corresponding<br />

unbinding transition of the filament bundle happens in a single,<br />

discontinuous transition.<br />

AKB 50.33 Fr 10:30 B<br />

Application of micron and nano scale metal island patterns as<br />

coordinative system for quantifying intracellular diffusion —<br />

•Tamas Haraszti and Joachim P. Spatz — University of Heidelberg,<br />

INF 253, 69120 Heidelberg<br />

Quantitative determination of intracellular diffusion in adhering cells<br />

allows access to evaluate dynamics important in cell functions. On very<br />

small length scales we face the problem that the absolute localisation of<br />

a diffusive probe such as fluorescent molecules or quantum dots in cells<br />

relative to the adhering substrate might fail. In our studies we correlate<br />

cellular diffusion to an absolute coordinative system made of micro and<br />

nano scale metal islands. Either e-beam or micellar diblock copolymer<br />

lithography applied to form the desired patterns. The patterns are iden-

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