Photo credit: © 2020 EPFL / Hillary Sanctuary

Date: 22 June 2020

Institution: École Polytechnique Fédérale de Lausanne

Study published in: Nature Methods

Digest: Detailed structure of centriole involved in animal cell division and cell movements, is visualized using a newly improved super-resolution fluorescent microscope developed by Biophysicists. Images produced by this microscope show post-translational modifications (PTMs), which were not visible through an electron microscope. The scientists also find a particular PTM that twists around the centriole ridges. They believe it has a role in centriole stability and functioning. This improved super-resolution fluorescent microscope with electron microscope images can increase our understanding of nanoscale structures of cell organelles.


“The symmetries of multi-molecular machines often explain how they can perform diverse functions. PTMs can form a special code that tells proteins where to dock, but can also stabilize the centriole while forces are pulling during division. We still don’t know why the twist is there, but it offers a clue to how centrioles work. Our study underlines that super-resolution microscopy is an important partner to electron microscopy for structural biology,” says biophysicist Suliana Manley who leads the Laboratory of Experimental Biophysics (LEB).

Super-resolution microscopy reveals a twist inside of cells

If you want to understand the underlying mechanisms of cellular motility and division, then the centriole is the organelle of interest. Each cell has a pair of centrioles which help to segregate chromosomes during cell division. These special organelles are multi-molecular machines composed of hundreds of proteins and have a hidden code of post-translational modifications (PTMs), that contribute to their rigidity or flexibility, which in turn may help explain how centrioles function.

Based on previous studies mostly using electron microscopy, the basic structure of centrioles is known. But PTMs are invisible to the electron microscope, so what do they look like?

Thanks to improved super resolution fluorescence microscope technology developed by EPFL biophysicists, we now have a detailed picture of these nanoscale structures, both isolated and in situ. As expected, the centrioles are shaped like ridged bullets, i.e. they are cylindrical with nine lengthwise ridges and their diameter tapers off at one end. Given this high degree of organization, the scientists were surprised to find that one PTM actually twists around these ridges. The results are published today in Nature Methods.

“The symmetries of multi-molecular machines often explain how they can perform diverse functions. PTMs can form a special code that tells proteins where to dock, but can also stabilize the centriole while forces are pulling during division. We still don’t know why the twist is there, but it offers a clue to how centrioles work. Our study underlines that super-resolution microscopy is an important partner to electron microscopy for structural biology,” says biophysicist Suliana Manley who leads the Laboratory of Experimental Biophysics (LEB).

Improved super resolution imaging techniques

Centrioles are about 100 times smaller than a mammalian cell, and a thousand times smaller than a human hair. So observing them inside of living cells required improving super-resolution microscope technology that uses light to probe specimens, since the methods tend to be too slow for structural studies. Dora Mahecic, a PhD student in the LEB, improved the illumination design to increase the size of images their microscope could capture by delivering light more uniformly across the field of view. 

The microscope, a super-resolution fluorescence microscope, is not at all the typical optical microscope that one would see in an introductory biology class. It is actually a complex setup of carefully aligned mirrors and lenses that shape and deliver laser light into the specimen. The biophysicists combined this setup with advanced sample preparation that uses physical magnification of the sample and fluorophores to make proteins, the building blocks of life, re-emit light.

This new super resolution technology could be used to study numerous other structures within the cell, like mitochondria, or to look at other multi-molecular machines such as viruses.


Story source: École Polytechnique Fédérale de Lausanne

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