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Here's how it works. The viral world can be divided into two types - enveloped and non-enveloped. Enveloped viruses are surrounded by the membrane of the cell it infected.
Non-enveloped viruses like polio emerge from an infected cell naked or without any membrane.
Enveloped viruses, like HIV and hepatitis C, use their membrane coating to fuse with cells and infect them. This is where scientists have found a way to disrupt the virus by using a small molecule called LJ-double-O-one.
In the lab, when scientists injected mice with this antiviral molecule, the molecules bound to the membranes of cells and viruses. While cells could repair their membranes from the damaging effects of LJ001, viruses could not.
That's because cells have the intercellular machinery they need to fix themselves - but viruses don't.
They're simply virus particles tucked into a cell's membrane, like a wolf in sheep's clothing. That's why the virus can't fix the damage done by LJ-double-o-one which in turn destroys the virus' ability to fuse with cells and infect them.
So far, LJ-double-o-one is shown to be effective against more than 20 viruses representing 11 groups. If human trials are successful, this tiny molecule could prevent or limit many viral diseases.
Publication: A broad-spectrum antiviral targeting entry of enveloped viruses
Mike C. Wolf, Alexander N. Freiberg, Tinghu Zhang, et al.
Primary journal article describing the initial characterization of LJ001 and how it inhibits a broad group of enveloped viruses.
Published online before print January 28, 2010, doi: 10.1073/pnas.0909587107