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Harnessed
with our partly unique microscopy and nanoscopy techniques, we are setting
out to explore the relationship between the structure and function of
selected cellular organelles, such as the mitochondria. At the same time,
we use our advanced techniques to map protein distributions at the highest
possible temporal and spatial resolution [6, 11, 26, 27].
The
animated graphic shows a surface reconstructed 3D-image of the GFP-tagged
mitochondrial matrix of a live budding yeast cell. The
cell wall is counterstained with the dye calcofluor white. Please
click on the animation to load a movie (5,4 MB).
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[6] |
Egner,
A., S. Jakobs and S. W. Hell (2002). "Fast 100-nm resolution
3D-microscope reveals structural plasticity of mitochondria in
live yeast." Proc. Natl. Acad. Sci. USA 99: 3370-3375.
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| [11] |
Jakobs, S.,
N. Martini, A. C. Schauss, A. Egner, B. Westermann and S. W. Hell
(2003). "Spatial and temporal dynamics of budding yeast mitochondria
lacking the division component Fis1p." J. Cell Sci. 116(10):
2005-2014. |
| [26] |
Jakobs, S.,
A. C. Schauss and S. W. Hell (2003). "Photoconversion of matrix
targeted GFP enables analysis of continuity and intermixing of the
mitochondrial lumen." FEBS Lett. 554: 194-200. |
[27] |
Messerschmitt, M., S. Jakobs, F. Vogel, S. Fritz, K. S. Dimmer,
W. Neupert and B. Westermann (2003). "The inner membrane
protein Mdm33 controls mitochondrial morphology in yeast."
J. Cell Biol. 160(4): 553-564.
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