New tool outsmarts COVID-19 virus to help vaccine development

Ensuring treatments remain effective as the virus mutates is a huge challenge for researchers. The powerful new tool harnesses genomic and protein information about the virus and its mutations to aid drug and vaccine development.

University of Melbourne Associate Professor David Ascher and his team at the Bio21 Molecular Science and Biotechnology Institute and the Baker Heart and Diabetes Institute developed the software tool and library, dubbed COVID-3D.

Published in Nature Genetics, COVID-3D contains information about all the protein structures that coincide with the SARS-CoV-2 (COVID-19) genome, including every known genetic mutation and its resultant mutant protein structure.

“Although the SARS-CoV-2 virus is a relatively new pathogen, its ability to readily accumulate mutations across its genes was evident from the start of this pandemic,” Associate Professor Ascher said.

“In the context of therapeutic drug design and discovery, these mutations, and the patterns by which they accumulate within the virus’ protein structures, can affect the ability of vaccines and drugs to bind the virus, or to create a specific immune response against it. Because of this, scientists must not only try to control the virus, but outsmart it by predicting how it will change over time.”

Several international universities and research institutions already use COVID-3D in vaccine and treatment development.

“At Bio21 it is being used as part of ongoing efforts to understand and develop drugs to treat COVID-19,” Associate Professor Ascher said.

To develop COVID-3D, Professor Ascher’s team analysed the genome sequencing data of over 120,000 SARS-CoV-2 samples from infected people globally, including those that uniquely affect Australia, to identify mutations within each of the virus’ proteins. They tested and analysed the mutations’ effects on their protein structure using computer simulations.

This data was used to calculate all the biological effects of every possible mutation within the genome. To help researchers account for possible future mutations, the team analysed mutations in the related coronaviruses SARS-CoV and Bat RaTG13.

Mutations or changes in an organism’s genetic material are natural ‘errors’ in the cell replication process. They can give the virus new ‘powers’ of survival, infectivity and virulence. Fortunately, the researchers found SARS-CoV-2 is mutating slower than other viruses such as influenza, with about two new changes in its genome every month.

COVID-3D can help researchers recognise how mutations operate and identify more effective vaccine and drug targets.

“It is only when you know how a mutation will affect the 3D shape of a protein, that you can predict if it will compromise your drug’s ability to bind,” Associate Professor Ascher said.

“As the global scientific and medical community gains better understanding of the biology behind the SARS-CoV2 infection and disease, this will be a powerful resource to predict problems with mutations and to guide the development of more effective therapies.

“COVID-3D continues to be updated with new protein structures, mutations and analyses to keep ahead of mutations that cause problems and increasing our understanding of the SARS-CoV-2 mechanisms of disease.”