Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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Arbeitskreis Biologische Physik Freitag<br />
modes. As a microscopic example a model of ion-channels with openclosing<br />
kinetics embedded in a biomembrane is presented. This model<br />
leads to generic amplitude equations occuring in systems with conserved<br />
order parameter and are furthermore studied in the general case of a<br />
simple reaction-diffusion system.<br />
AKB 50.115 Fr 10:30 B<br />
Hopf-bifurcations in systems with conserved quantities —<br />
•Markus Hilt and Walter Zimmermann — Theoretische Physik,<br />
Universität des Saarlandes, 66041 Saarbrücken<br />
A cubic Ginzburg–Landau equation is presented, which describes for<br />
the first time the universal properties of a Hopf-bifurcation in a system<br />
with conserved quantities. This bifurcation occurs for instance in a model<br />
describing the dynamics of two interacting ion-channels in a membrane.<br />
It is a universal feature of this bifurcation that all nonlinear traveling<br />
wave solutions are linear unstable in general, besides the smallest possible<br />
wavenumber in a finite system with periodic boundary conditions.<br />
Spatio-temporal chaos occurs either due to boundary effects or due to<br />
an extension of the destabilizing wavenumber band. This scenario is different<br />
from other cases, where spatio-temporal chaos often occurs, as for<br />
instance for one of the most studied nonlinear equations in physics, the<br />
Ginzburg–Landau equation for unconserved systems (see e.g. I. Aranson<br />
and L. Kramer, Rev. Mod. Phys. 74, 99 (2002)).<br />
AKB 50.116 Fr 10:30 B<br />
Fluorescence Excitation Spectroscopy on Single Light-<br />
Harvesting Complexes of Higher Plants — •Carsten Tietz 1 ,<br />
Sebastian Schuler 1 , Fedor Jelezko 1 , Heiko Lokstein 2 ,<br />
and Jörg Wrachtrup 1 — 1 3. Physikalisches Institut, Universität<br />
Stuttgart, 70550 Stuttgart, Germany — 2 Institut für Pflanzenphysiologie,<br />
Humboldt-Universität Berlin, 10099 Berlin, Germany<br />
Photosynthesis of higher plants and green algae is the most important<br />
metabolic process on earth. The absorption of light in higher plants is<br />
carried out by pigment-protein complexes. Besides the well known major<br />
Light-Harvesting Complex II (LHCII) that exists in a trimeric form<br />
there are several minor chlorophyll (Chl) a and b binding complexes to<br />
be found in Photosystem 2.<br />
Single molecule spectroscopy has been used to investigate the photophysics<br />
of the minor plant antenna CP29 in its native monomeric form.<br />
This complex binds 8 chlorophylls of which 2 are supposed to be Chl<br />
b and 6 Chl a. Although the structure is not known, sequence analysis<br />
showed a strong resemblance between LHCII monomers and CP29.<br />
Therefore it was possible to construct a structural model of CP29 on the<br />
basis of LHCII.<br />
With combined excitation and emission spectra of single CP29 complexes<br />
at low temperatures (2 K), we can gather information about the<br />
energy levels of the bound Chl molecules, the relative orientation of their<br />
transition dipole moments and the energy transfer rate. Here we report<br />
on the first fluorescence excitation spectra of single CP29 complexes.<br />
AKB 50.117 Fr 10:30 B<br />
Cell Adhesion onto Highly Curved Particle Surfaces - One-<br />
Step Immobilization of Cell Membranes — •Motomu Tanaka<br />
und Stefan Kaufmann — Biophysics Lab, Tech. Univ. Munich<br />
We report single-step, orientation selective immobilization of human<br />
erythrocyte membranes on bare silica beads with different topographies:<br />
1) solid (nonporous) silica beads with a diameter of 3 microns and 2) porous<br />
silica beads with a diameter of 5 microns. Erythrocyte membranes<br />
were immobilized onto beads simply by incubation, without sonication or<br />
osmotic lysis. Membrane orientation before and after the immobilization<br />
was identified with a first monoclonal antibody and a second fluorescent<br />
polyclonal antibody. Adherent erythrocytes on the beads all ruptured,<br />
inverted the asymmetric orientation of the membrane, and selectively<br />
exposed their cytoplasmic domain. The surface topography did not influence<br />
orientation or the amount of immobilized membranes. On the other<br />
hand, the fact that no adsorption or rupture of erythrocytes could be<br />
observed on planar quartz substrates suggests a significant influence of<br />
contact curvatures on the adhesion free energy.<br />
AKB 50.118 Fr 10:30 B<br />
Analysis of Spatiotemporal Data Sets in Dictyostelium —<br />
•Christiane Hilgardt 1 , Marc-Thorsten Hütt 2 , and Stefan C.<br />
Müller 1 — 1 Otto-von-Guericke Universität Magdeburg, Institut für<br />
Experimentelle Physik, Abteilung Biophysik, Universitätsplatz 2, 39106<br />
Magdeburg — 2 Technische Universität Darmstadt, Institut für Botanik,<br />
Arbeitsgruppe Theoretische Biologie und Bioinformatik, Schnittspahnstraße<br />
3, 64287 Darmstadt<br />
We investigate reaction-diffusion waves in the slime mould Dictyostelium<br />
with spatiotemporal analysis filters, [1, 2, 3]. Our hypothesis<br />
is that the spatial distribution of cell properties determines the architecture<br />
of structures in later morphogenetic stages, e.g. aggregation<br />
streams. Our investigations address the constructive role of variability<br />
in biological structure formation. To this goal we visualize local inhomogeneities<br />
in fluctuations, which allow to distinguish between fast and<br />
directed dynamics. We correlate extremal behavior with later structures.<br />
In particular, we focus on the borders between the different states of<br />
an excitable medium (excitable, excited and refractory) to evaluate biological<br />
variability as the ”roughness” of these border lines. First results<br />
support our hypothesis. The spatial distribution of our observable shows<br />
an elevated correlation with the position of later aggregation streams.<br />
Furthermore, methods of information theory and estimation theory from<br />
sequence analysis are developed and applied to the spatiotemporal data<br />
sets. [1] Müller S. C. et al. (1998) Biophys. Chem. 72: 37-47. [2] Hütt<br />
M.-Th., Neff R. (2001) Physica A 289: 498-516. [3] Hütt M.-Th. et al.<br />
(2002) Phys. Rev. E. 66: 26117.<br />
AKB 50.119 Fr 10:30 B<br />
Functional Micro-Domains of Glycolipids with Partially Fluorinated<br />
Membrane Anchors - Impact on Cell Adhesion —<br />
•Motomu Tanaka 1 , Matthias Schneider 1 , Laurent Limozin 1 ,<br />
Doris Heinrich 1 , Gabriele Schumacher 2 , Gerd Bendas 2 , Ulrich<br />
Rothe 3 , Christian Gege 4 , and Richard Schmidt 4 — 1 Dept.<br />
Physics E22, Tech. Univ. Munich — 2 Dept. Pharmacy, Univ. Bonn —<br />
3 Dept. Physiol. Chem., Univ. Halle — 4 Dept. Chem., Univ. Konstanz<br />
Functional micro-domains of glycolipids were designed by mixing neoglycolipids<br />
with partially fluorinated (F-alkyl) chains and matrix lipids<br />
with alkyl chains. Fluorescence images of the mixed lipid monolayers<br />
at air/water interface demonstrated that it is possible to control both<br />
size and distribution of the micro-domains according to the strong demixing<br />
of alkyl and F-alkyl membrane anchors, while the correlation<br />
between carbohydrate head groups seemed to play rather minor roles.<br />
These micro-domains in monolayers could be transferred onto hydrophobized<br />
substrates, and subjected to dynamic flow chamber experiments.<br />
The results obtained here clearly indicated that the dynamic adhesion of<br />
Chinese hamster ovarial cells expressing E-selectin (CHO-E cells) onto<br />
the lipid monolayer containing micro-domains of sialyl LewisX (sLeX)<br />
can be both enhanced and reduced by controlled de-mixing of ligands<br />
and matrices. Moreover, the same clusters of sLeX could also be formed<br />
in giant lipid vesicles, which can be used as a model cell that locally<br />
expresses bio-specific functions.<br />
AKB 50.120 Fr 10:30 B<br />
Functional Micro-Domains of Glycolipids with Partially Fluorinated<br />
Membrane Anchors - Impact on Cell Adhesion —<br />
•Motomu Tanaka 1 , Matthias Schneider 1 , Laurent Limozin 1 ,<br />
Doris Heinrich 1 , Gabriele Schumacher 2 , Gerd Bendas 2 , Ulrich<br />
Rothe 3 , Christian Gege 4 , and Richard Schmidt 4 — 1 Dept.<br />
Physics E22, Tech. Univ. Munich — 2 Dept. Pharmacy, Univ. Bonn —<br />
3 Dept. Physiol. Chem., Univ. Halle — 4 Dept. Chem., Univ. Konstanz<br />
Functional micro-domains of glycolipids were designed by mixing neoglycolipids<br />
with partially fluorinated (F-alkyl) chains and matrix lipids<br />
with alkyl chains. Fluorescence images of the mixed lipid monolayers<br />
at air/water interface demonstrated that it is possible to control both<br />
size and distribution of the micro-domains according to the strong demixing<br />
of alkyl and F-alkyl membrane anchors, while the correlation<br />
between carbohydrate head groups seemed to play rather minor roles.<br />
These micro-domains in monolayers could be transferred onto hydrophobized<br />
substrates, and subjected to dynamic flow chamber experiments.<br />
The results obtained here clearly indicated that the dynamic adhesion of<br />
Chinese hamster ovarial cells expressing E-selectin (CHO-E cells) onto<br />
the lipid monolayer containing micro-domains of sialyl LewisX (sLeX)<br />
can be both enhanced and reduced by controlled de-mixing of ligands<br />
and matrices. Moreover, the same clusters of sLeX could also be formed<br />
in giant lipid vesicles, which can be used as a model cell that locally