Human cells are very complex entities with many different components. A very important cellular component are the ribosomes: As the protein factories of the cell, they are responsible for the production of proteins (protein synthesis). The blueprint provides our heritable information, the DNA.
Because of their importance for protein synthesis, the ribosomes have often been subject of structural research. Until now, the scientists could only look at individual, isolated ribosomes. But in the living cell, ribosomes usually appear lined up like pearls on a string, in so-called polyribosomes. An isolated view is not enough to understand completely how the protein production proceeds inside the cell and how it is embedded in the complex cellular structures and processes. Thus it is necessary to map and to investigate the ribosomes in their “natural environment”, in the interior of the cell. This permits cryo-electron tomography.
With this method, which was mainly developed in the department of Molecular Structural Biology, headed by Wolfgang Baumeister, three-dimensional cellular structures can be mapped and examined. The cell is sort of quick-frozen, so that its spatial structure remains and its properties are not modified. Then the scientists use the electron microscope to record twodimensional pictures of the cell from different perspectives. From these pictures they finally reconstruct a three-dimensional image. By using this method, the MPIB scientists were able to create a three-dimensional map of an intact human cell for the first time. This is the continuation of former work, when the team around Wolfgang Baumeister and F.-Ulrich Hartl already managed to analyze the spatial arrangement of polyribosomes in the bacterium E. coli (Brandt et al., Cell 2009) and of inactivated ribosomes in a whole E. coli cell (Ortiz et al., JCB
2010).
Now the scientists discovered how the ribosomes are positioned inside the human cell: Their arrangement is clearly non-random but rather makes sure that newly originated, still unfolded proteins keep a big distance between each other. “We could already observe a similar positioning in bacterial cells which suggests that the ribosomes of all human beings are arranged in almost the same manner”, explains Florian Brandt, scientist at the MPIB. “This spatial organization of the ribosomes could probably have the aim to inhibit the aggregation and misfolding of newly originated proteins.”
The work of the MPIB scientists is another important step for cell biology, because it helps to better understand the distribution of cellular components and the spatial organization of the whole cell much better. “In the future it could also be interesting”, says Brandt, “how the organization of ribosomes changes in aging and sick cells and how these changes affect the total efficiency of protein production and folding.”
Original Publication:
Florian Brandt, Lars-Anders Carlson, F.-Ulrich Hartl, Wolfgang Baumeister and Kay Grünewald: The three-dimensional organization of polyribosomes in intact human cells. Molecular Cell, August 27, 2010.
Contact:
Prof. Dr. Wolfgang Baumeister
Molecular Structural Biology
Max Planck Institute of Biochemistry
Am Klopferspitz 18
82152 Martinsried, Germany
E-mail: baumeist@biochem.mpg.de
Dr. Kay Grünewald
The Division of Structural Biology
University of Oxford
The Henry Wellcome Building for Genomic Medicine
Roosevelt Drive
Oxford, OX3 7BN
United Kingdom
E-mail: kay@strubi.ox.ac.uk
Anja Konschak
Public Relations
Max Planck Institute of Biochemistry
Am Klopferspitz 18
82152 Martinsried, Germany
Phone ++49/89-8578-2824
E-mail: konschak@biochem.mpg.de
www.biochem.mpg.de
(idw, 09/2010)