Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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-