Cure for `deadly` Ebola virus comes closer to reality
Washington: Scientists have been able to uncover the molecular mechanism by which the deadly Ebola virus assembles, providing potential new drug targets.
The study also showed that the same molecule that assembles and releases new viruses also rearranges itself into different shapes, with each shape controlling a different step of the virus`s life cycle.
Erica Ollmann Saphire, Ph.D., professor in the Department of Immunology and Microbial Science at TSRI, said that like a `Transformer`, this protein of the Ebola virus adopts different shapes for different functions.
He asserted that it revises a central dogma of molecular biology-that a protein molecule has one shape that predestines one biological function."
Zachary Bornholdt, Ph.D., senior staff scientist and first author of the study, said that drugs to block viral replication could target any of the structures themselves or the intermediate steps in the structural transformation process.
Ebola hemorrhagic fever is one of the most virulent diseases known to humankind. Very few pathogens prove more dangerous than Ebola virus once a person is infected. There is no cure, and the case-fatality rate can be up to 90 percent, depending on which strain is involved.
To conduct the study, Dr. Saphire and her group at TSRI collaborated with Yoshihiro Kawaoka , Ph.D., D.V.M., who holds joint appointments at the University of Wisconsin and University of Tokyo.
Dr. Kawaoka`s group provided cellular microscopy and critical replication experiments to complement the TSRI team`s expertise in x-ray crystallography and protein biochemistry.
The results, five years in the making, revealed the Ebola VP40 protein exists as a dimer, not as a monomer as previously thought, and it rearranges its structure to assemble filaments to build the virus shell or "matrix" to release countless new viruses from infected cells.
The study showed the protein also rearranges itself into rings in order to bind RNA and control the internal components of the virus copied inside infected cells.
This "shape-shifting" or "transformer" behavior explains how the Ebola virus can control a multi-step viral lifecycle using only a very limited number of genes.
The study has been published in the peer-reviewed journal Cell.