Super-res microscope explores living cells in 3D noninvasively

A startup company founded last year at the École Polytechnique Federale de Lausanne (EPFL) Innovation Park in Switzerland, Nanolive SA, has developed a super-resolution microscope that enables exploration of a living cell in 3D without damaging it.

Content Dam Bow Online Articles 2014 11 Nanolive 1 Web

A startup company founded last year at the École Polytechnique Federale de Lausanne (EPFL) Innovation Park (Lausanne, Switzerland), Nanolive SA, has developed a super-resolution microscope that enables exploration of a living cell in 3D without damaging it.

Related: Light absorption indicates oxidative stress in cells

While scientists may still obtain a finer resolution using an electron microscope, this approach cannot be used to examine cells that are alive. For a long time, it was believed to be impossible to look inside a living cell using light microscopes due to their physical limitations. This year's Nobel Prize for Chemistry was awarded to Stefan Hell, Eric Betzig, and William Moerner, who did not believe these presumed limitations and made revolutionary discoveries in the field of fluorescence microscopy.

While their research was focused on the chemistry of single molecules and their pathways inside living cells, Nanolive focuses on the physical structure of the living cell itself.

Content Dam Bow Online Articles 2014 11 Nanolive 1 Web
A mouse reticular fibroblast imaged with the 3D Cell Explorer super-resolution microscope.

The 3D Cell Explorer super-resolution microscope peers into living cells without sample preparation, enabling noninvasive observation of nuclei and organelles down to 70 nm. Similar to a magnetic resonance imaging (MRI)/computed tomography (CT) scan, the microscope takes a complete tomographic image of the refractive index within living cells, allowing researchers to see and precisely measure the impact of stimuli and drugs on cells.

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A fixed fibroblast chemically stained to identify membrane (green) and nucleus (blue). To the right is the same cell imaged with Nanolive's 3D Cell Explorer, stained only digitally. In the first case, the preparation procedure killed the cell and took more than four hours. Using Nanolive's technology, the same result took just five minutes and would have been possible on unstained, living cells.

For more information, please visit http://nanolive.ch/product.

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