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Fast 100-nm Resolution Three-Dimensional Microscope Reveals Structural Plasticity of Mitochondria in Live Yeast
Alexander Egner, Stefan Jakobs and Stefan W. Hell
Proceedings of the National Academy of Sciences of the United States of America
Vol. 99, No. 6 (Mar. 19, 2002), pp. 3370-3375
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/3058133
Page Count: 6
You can always find the topics here!Topics: Mitochondria, Fluorescence, Microscopes, Microscopy, Imaging, Hell, Yeasts, Diameters, Mother cells, Daughter cells
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By introducing beam-scanning multifocal multiphoton 4Pi-confocal microscopy, we have attained fast fluorescence imaging of live cells with axial super resolution. Rapid scanning of up to 64 pairs of interfering high-angle fields and subsequent confocal detection enabled us to perform three to five times finer optical sectioning than confocal microscopy. In conjunction with nonlinear image restoration, we demonstrate, to our knowledge for the first time, three-dimensional imaging of live eukaryotic cells at an equilateral resolution of ≈100 nm. This imaging mode allowed us to reveal the morphology and size of the green fluorescent protein-labeled mitochondrial compartment of live Saccharomyces cerevisiae (bakers' yeast) growing on different carbon sources. Our studies show that mitochondria of cells grown on medium containing glycerol as the only carbon source, as opposed to glucose-grown cells, exhibit a strongly branched tubular reticulum. We determine the average tubular diameter and find that it increases from 339 ± 5 nm to 360 ± 4 nm when changing from glucose to glycerol, that is, from a fermentable to a nonfermentable carbon source. Moreover, this change is associated with a 2.8-fold increase of the surface of the reticulum, resulting in an average increase in volume of the mitochondrial compartment by a factor of 3.0 ± 0.2.
Proceedings of the National Academy of Sciences of the United States of America © 2002 National Academy of Sciences