This rendering shows a 3-D reconstruction of a Mimivirus, based on an analysis of data obtained in an experiment at SLAC's Linac Coherent Light Source X-ray laser that show the electron density of an intact Mimivirus, a type of giant virus. The blue regions represent the areas of highest density.
The experiment at SLAC’s Linac Coherent Light Source (LCLS), a DOE Office of Science User Facility, establishes a new technique for reconstructing the 3-D structure of many types of biological samples from a series of X-ray laser snapshots.
“Ever since I started in this field of X-ray laser research, this has always been the dream – to acquire 3-D images of real biological samples,” said Tomas Ekeberg, a biophysicist at Uppsala University in Sweden and lead author of the study, published March 2 in Physical Review Letters. “This is fantastic – it’s a breakthrough in our research.”
Mimivirus is so big – its volume is thousands of times larger than the smallest viruses and even larger than some bacteria – that it was misclassified as a bacterium until 2003. Subsequent discoveries have found other giant viruses, some of which are even larger.
Mimivirus is also genetically complex, with nearly 1,000 major genes compared to only a handful in the HIV virus.
Scientists have been trying to determine the inner structure of these giant viruses to learn more about their origins: For example, did they borrow genes over time from the host organisms they infect, like amoebas? Did they precede cell-based life or devolve from cell-based organisms?
In the LCLS experiment, researchers sprayed a gas-propelled aerosol containing active Mimivirus samples in a thin stream into the X-ray laser beam, which scattered off the viruses and produced light patterns on a detector that were recorded as diffraction images.
Researchers customized sophisticated analysis software developed at Cornell University to compile hundreds of individual images from separate virus particles into a single 3-D portrait showing the general shape and inner features of Mimivirus. Each image captured a projection of a separate virus particle at a random orientation, so the collection of images of viruses in different orientations provided a more complete, 3-D view.
While the technique used at LCLS did not provide high-resolution details of the internal virus structure, it did confirm that its contents are lopsided, with an area that appears more densely concentrated. “We can see quite clearly that the inside of these viruses is not uniform,” Ekeberg said.
This same general feature had also been seen before using an electron-based imaging technique with frozen samples, and LCLS allows studies of viruses and other biological samples in a more natural, intact state. Researchers said that LCLS shows promise for achieving sharper images that reveal more inner details in the future because of the uniquely intense, penetrating power of its X-rays.
The same technique was recently used to study bacterial cell structures. LCLS managers have launched an initiative with the scientific community to improve techniques for imaging intact, biological particles that are difficult to study.
Janos Hajdu, a professor of biophysics at Uppsala and a pioneer in biological particle imaging with X-ray lasers, said the research team plans to apply the 3-D imaging technique to other types of samples and to improve the image quality. He said, “The next Holy Grail is to study large, single proteins at LCLS.”
Source: Press release Uppsala University