Scientists Identify Drug Targets For Pan-Coronavirus Treatment

Scientists have identified the most highly conserved drug-binding pockets in viral proteins from COVID-19 patient samples and from other coronaviruses, revealing the most promising targets for pan-coronavirus drugs.

The researchers from the University of Toronto in Canada noted that safe and effective vaccines offer hope for an end to the COVID-19 pandemic.

However, the possible emergence of vaccine-resistant SARS-CoV-2 variants, as well as novel coronaviruses, make finding treatments that work against all coronaviruses as important as ever, they said.

The study, published in the Journal of Proteome Research, analysed viral proteins across 27 coronavirus species and thousands of samples from COVID-19 patients.

It identified highly conserved sequences that could make the best drug targets.

Drugs often bind inside "pockets" on proteins that hold the drug snugly, causing it to interfere with the protein's function.

Scientists can identify potential drug-binding pockets from the three dimensional (3D) structures of viral proteins.

However, over time, viruses can mutate their protein pockets so that drugs no longer fit.

The researchers noted that some drug-binding pockets are so essential to the protein's function that they cannot be mutated, and these sequences are generally conserved over time in the same and related viruses.

They used a computer algorithm to identify drug-binding pockets in the 3D structures of 15 SARS-CoV-2 proteins.

The team found corresponding proteins in 27 coronavirus species and compared their sequences in the drug-binding pockets.

The two most conserved druggable sites were a pocket overlapping the RNA binding site of the helicase nsp13, and a binding pocket containing the catalytic site of the RNA-dependent RNA polymerase nsp12.

Both of these proteins are involved in viral RNA replication and transcription.

The drug-binding pocket on nsp13 was also the most highly conserved across thousands of SARS-CoV-2 samples taken from COVID-19 patients, with not a single mutation.

The researchers noted that novel antiviral drugs targeting the catalytic site of nsp12 are currently in phase II and III clinical trials for COVID-19.

The RNA binding site of nsp13 is a previously underexplored target that should be a high priority for drug development, they added.

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