
Remdesivir is the first drug against COVID-19 to be conditionally approved in Europe and the United States.
The drug is designed to suppress the rapid replication of the SARS-CoV-2 virus in human cells by blocking the viral copying machine, called RNA polymerase.
In a new study, researchers found how remdesivir interferes with the viral polymerase during copying and why it does not inhibit it completely.
They found remdesivir does interfere with the polymerase while doing its work, but only after some delay. And the drug does not fully stop the enzyme.
The research was conducted by a team at the Max Planck Institute (MPI) for Biophysical Chemistry and elsewhere.
At the pandemic’s beginning, the team had elucidated how the coronavirus duplicates its RNA genome.
For the pathogen this is a colossal task as its genome comprises around 30,000 RNA building blocks, making it particularly long.
They found remdesivir’s structure resembles that of RNA building blocks. The polymerase is thereby misled and integrates the substance into the growing RNA chain.
After remdesivir had been incorporated into the viral genome, the researchers examined the polymerase-RNA complexes using biochemical methods and cryo-electron microscopy.
They discovered that the copying process pauses precisely when three more building blocks have been added after remdesivir was incorporated into the RNA chain.
This pausing is caused by only two atoms in the structure of remdesivir that get hooked at a specific site on the polymerase. However, remdesivir does not fully block RNA production.
Often, the polymerase continues its work after correcting the error.
Understanding how remdesivir works opens up new opportunities for scientists to tackle the virus.
The new findings may help improve the substance and its effect.
In addition, the researchers want to search for new compounds that stop the viral copying machine.
They say the vaccinations now underway are essential to bringing the pandemic under control.
But scientists also need to develop effective drugs that mitigate COVID-19 disease progression in the event of infection.
One author of the study is Max Planck Director Patrick Cramer.
The study is published in Nature Communications.
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