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Schwille Group
(Visit the group site)
Scientific Profile
Our group is primarily concerned with the development and application of
novel spectroscopic and microscopic techniques for the quantitative
investigation of sparse and single molecules in solution and living
cells. Additionally, we aim for the design of appropriate
fluorescence-based protein and enzyme assays for rapid but
ultrasensitive characterization. In addition to basic research, the
integration of such ultrasensitive detection modules in so-called
lab-on-a-chip microfluidic structures is pursued, to facilitate
manipulation of minute analyte quantities, subsequent to multiparameter
fluorescence analysis. The ultimate goal here is to rapidly and
efficiently select cells and molecules with desired characteristics from
large heterogeneous libraries.
Motivation and Techniques
Scientific discoveries are often stimulated by the invention of new
scientific tools. The enormous progress in the life sciences in recent
years is a direct result of the emergence of new powerful bioanalytical
technologies. At the dawn of the modern proteomics age, methods are
required which greatly simplify the quantitative analysis of protein
dynamics and interactions. Ideally, different kinds of proteins should
be directly and simultaneously observed in their native environment,
i.e., the living cell or even organism, at physiological, i.e. mostly
submicromolar, concentrations. Single molecule fluorescence microscopy
and spectroscopy, relatively young disciplines at the interface of
physics, chemistry and biology, provide excellent conditions for such
investigations. During the past years, confocal fluorescence correlation
spectroscopy (FCS) and related techniques have enabled us to study a
masnifold of different parameters such as diffusion and transport rates,
molecular association and dissociation, enzyme dynamics and
intramolecular dynamics in vitro, but also in the living cell. Employing
cross-correlation schemes and nonlinear fluorescence excitation modes,
many different fluorescent species can be observed simulateously.
Fluorescence lifetime and anistotropy measurements can further be
integrated as they add even more information. In the context of basic
cell biological research, these novel techniques open up fascinating
perspectives to unravel complex intracellular processes involving
multiple species of biomolecules, such as signal transduction and
protein trafficking with high spatial and temporal precision. Besides
the scientific relevance for single molecule analysis in physics,
chemistry and biology, these techniques are of increasing importance
also in pharmacologic drug screening. One challenge here is the
miniaturized manipulation and selection of biomolecules with respect to
their individual properties. The requirement of only minute amounts of
analytes without having to synchronize their dynamics, and the
possibility to distinguish subpopulations of molecular species which
would in bulk analysis be hidden in a statistic mean, open up great
perspectives for high-throughput screening applications. To this end, we
combine our detection modules with home-designed microfluidic structures
of various transparent materials, fabricated by means of standard
litographic processes.
See also
www.biophysik-dresden.de.
Selected Publications
2005
Chiantia S., Kahya N., Schwille P. (2005) Dehydration damage of domain-exhibiting supported bilayers: an AFM study on the protective effects of disaccharides and other stabilizing substances.
Langmuir. 2005; 21(14):6317-23.
Kim S.A., Heinze K.G., Bacia K., Waxham M.N., Schwille P. (2005) Two -photon cross-correlation analysis of intracellular reactions with variable stoichiometry,
Biophys J. 2005 88(6), 4319-4336
Kahya N., Scherfeld D., and Schwille P. (2005) Differential lipid packing abilities and dynamics in giant unilamellar vesicles composed of saturated glycerophospholipids,
sphingomyelin and cholesterol, Chem. Phys. Lipids in press
Bacia K., Schwille P., and Kurzchalia T. (2005) Sterol structure determines the separation of phases and the curvature of the
liquid-ordered phase in model membranes, Proc. Natl. Acad. Sci. USA, 102(9), 3272-3277
Schwille, P., Kahya, N., Bacia, K. (2005) Lipid and Protein Partitioning Between Raft and Non-Raft Lipid Mixtures,
Chapter in: Protein-Lipid Interactions, Wiley-VCH, ed. Lukas K. Tamm, in press
Berezhna S. Schaefer S. Heintzmann R. Jahnz M. Boese G. Deniz A. Schwille P. (2005) New effects in polynucleotide release from cationic lipid
carriers revealed by confocal imaging, fluorescence cross-correlation spectroscopy and single
particle tracking BBA -Biomembranes, 1669(2):193-207
Dittrich, P.S., Jahnz, M., and Schwille, P. (2005) A New Embedded Process for Compartmentalized Cell-free Protein Expression and On-line Detection in Microfluidic Devices, ChemBioChem, 6, 811-814
Stagi, M., Dittrich, P.S., Frank N., Iliev, A.I., Schwille, P. and Neumann, H. (2005) Breakdown of axonal synaptic vesicle precursor
transport by microglial nitric oxide, J. Neuroscience, 25, 352-362
Jahnz M., and Schwille P. (2005) A Novel Homogenous Assay for Topoisomerase II Action and Inhibition, ChemBioChem, 6(5), 920-926.
Jahnz, M., Schwille, P., (2005) An ultrasensitive site-specific DNA recombination assay based on dual-color fluorescence cross-correlation spectroscopy,
Nucleic Acids Research. 33(6):E60.
Gordon, S.P. Berezhna, S., Scherfeld, D., Kahya, N., and Schwille, P. (2005) Characterization of Interaction between
Cationic Lipid-Oligonucleotide Complexes and Cellular Membrane Lipids
Using Confocal Imaging and Fluorescence Correlation Spectroscopy, Biophys. J. 88: 305-316
Kohl T. and Schwille P. (2005) Fluorescence Correlation Spectroscopy with autofluorescent proteins. Adv. Biochem. Biotechnol., in press
Becker, W., Bergmann, A., Haustein, E., Petrasek, Z., Schwille, P., Biskup, C., Anhut, T., Riemann, I., K�ig, K. (2005) Fluorescence lifetime images and correlation
spectra obtained by multi-dimensional TCSPC. Proceedings of Spie, 5700, 2005 in press
Becker, W., Bergmann, A., Haustein, E., Petrasek, Z., Schwille, P., Biskup, C., Anhut, T., Riemann, I., K�ig, K. (2005)
Fluorescence lifetime images and correlation spectra obtained by multi-dimensional TCSPC. Mic. Res. Tech., 2005 in press
Kohl, T. Haustein, E. Schwille, P. (2005) Determining protease activity in vivo by fluorescence cross-correlation analysis.
Biophysical Journal in press
Schwille, P., Heinze, K. G., Dittrich, P., Haustein, E. (2005) Two-photon Fluorescence Correlation Spectroscopy.
In Biomedical Optical Imaging. Fujimoto, J. G. and Farkas, D. (Hrsg.). Oxford University Press, 2005.
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Petra Schwille
PhD 1996 Max-Planck-
Inst. for Biophysical
Chemistry, Göttingen/
TU Braunschweig
1997-1999
Postdoctoral work
at Cornell University,
Ithaca, NY
1999-2002 Junior
group leader at the
MPIbpc Göttingen
2002-present
Professor of Bio-
physics at the TU
Dresden
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