Retroviruses essentially consist of genetic material encased in a protein shell, which is in turn surrounded by a membrane. After entering a target cell – in the case of HIV, one of the cells in our immune system – the virus replicates, producing more copies of itself, each of which has to be assembled from a medley of viral and cellular components into an immature virus.
“All the necessary components are brought together within the host cell to form the immature virus, which then has to mature into a particle that’s able to infect other cells” says John Briggs, who led the research at EMBL. “We found that when it does, the changes to the virus’ shell are more dramatic than expected.”
Both the mature and immature virus shells are honeycomb-like lattices of hexagon-shaped units. Using a combination of electron microscopy and computer-based methods, Briggs and colleagues investigated which parts of the key proteins stick together to build the honeycomb of the immature shell. These turned out to be very different from the parts that build the mature shell. This knowledge will help scientists to unravel how the immature virus is assembled in the cell and how the shell proteins rearrange themselves to go from one form to the other.
Findings such as these may one day prove valuable to those wanting to design new types of anti-retroviral therapies. Many anti-retroviral drugs already block the enzyme that would normally separate components of the immature shell to allow it to mature. But there are currently no approved drugs that act on that shell itself and prevent the enzyme from locking on.
Although the virus shells imaged in this study were derived from the Mason-Pfizer monkey virus and made artificially in the laboratory, they closely resemble those of both this virus and HIV – which are very similar – in their natural forms.
“We still need a lot more detailed information before drug design can really be contemplated,” Briggs concludes, “but finally being able to compare mature and immature structures is a step forwards.”
The work was done in collaboration with the group of Tomas Ruml at the Institute of Chemical Technology in Prague, Czech Republic.
Republished with permission from the European Molecular Biology Laboratory.