Bio21 Molecular Science & Biotechnology Institute - Molecular Biology https://www.bio21.unimelb.edu.au/tags/molecular-biology en Media Release: New tool outsmarts COVID-19 virus to help vaccine development https://www.bio21.unimelb.edu.au/media-release-new-tool-outsmarts-covid-19-virus-help-vaccine-development <div class="field field-name-field-image field-type-image field-label-hidden"><div class="field-items"><div class="field-item even"><img typeof="foaf:Image" src="https://www.bio21.unimelb.edu.au/sites/www.bio21.unimelb.edu.au/files/styles/page/public/field/image/2020-09-09-Bio21_Web_David-Ascher.jpg?itok=9pPf6wfo" width="960" height="440" alt="" /></div></div></div><div class="field field-name-body field-type-text-with-summary field-label-hidden"><div class="field-items"><div class="field-item even" property="content:encoded"><h1 style="margin-top:16px; margin-bottom:4px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">9 September 2020</span></span></h1> <h1 style="margin-top:16px; margin-bottom:4px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">Melbourne researchers have developed a tool to monitor mutations that make it difficult to develop coronavirus (COVID-19) vaccines and drugs.</span></span></h1> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">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. </span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">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. </span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">Published in <a href="https://www.nature.com/articles/s41588-020-0693-3" style="color:black; text-decoration:underline"><i>Nature Genetics</i></a>, 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. </span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">“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. </span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">“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.”</span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">Several international universities and research institutions already use COVID-3D in vaccine and treatment development.<span style="font-size:11.0pt"><span style="color:#201f1e"> “A</span></span>t Bio21 it is being used as part of ongoing efforts to understand and develop drugs to treat COVID-19,” Associate Professor Ascher said.</span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">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.</span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">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. </span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">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. </span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">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.</span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">“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. </span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif">“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.” </span></span></p> <p style="margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif"><b>Media enquiries: Cheryl Critchley | 0418 312 596 | </b><a href="about:blank" style="color:black; text-decoration:underline"><b><span class="spamspan"><span class="u">cheryl.critchley</span> [at] <span class="d">unimelb.edu.au</span></span></b></a><br /><b>Study link: </b><a href="about:blank" style="color:black; text-decoration:underline" target="_blank"><span style="border:none windowtext 1.0pt; font-size:11.0pt; padding:0cm"><span style="background:white"><span style="color:blue">http://dx.doi.org/10.1038/s41588-020-0693-3</span></span></span></a></span></span></p> <div style="border:solid windowtext 1.0pt; padding:1.0pt 4.0pt 1.0pt 4.0pt"> <p style="border:none; padding:0cm; margin-bottom:8px"><span style="font-size:10pt"><span style="font-family:Calibri,sans-serif"><b><span style="font-size:9.0pt">What happens when a gene mutates? </span></b><span style="font-size:9.0pt">Each gene encodes the recipe to make a specific protein. Unlike DNA or RNA, which are like wound-up pieces of ribbon, proteins have three dimensional structures. Their 3D undulating surfaces appear like mountains and valleys, pockets, and grooves. Drugs and antibodies recognise and bind to specific locations on this surface, similar to a key fitting into a lock. A mutated gene can change the shape of the protein. If it alters the shape of the lock, it can mean that the drug or antibody no longer ‘fits’ to the virus protein.  Because therapies like vaccines and drugs target proteins specifically, mutations that compromise drug interactions present a major challenge in therapeutic drug and vaccine development, potentially rendering these therapies ineffective. </span></span></span></p> </div> </div></div></div> Tue, 08 Sep 2020 14:00:00 +0000 floder 478 at https://www.bio21.unimelb.edu.au