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05/31/2022 17:07

A precision cut for the CRISPR-Cas genetic scissors

Susanne Thiele Presse und Kommunikation
Helmholtz-Zentrum für Infektionsforschung

    A new study indicates how deep learning can improve gene therapies and antiviral drugs

    The nuclease Cas13b associated with CRISPR defense systems—also known as genetic scissors—has the potential to be used in the future in hereditary diseases to silence adverse genes. In the fight against infections, it is also being researched as an antiviral agent, as Cas13b can target the genome of viruses and render them harmless. Despite these promising features, researchers are looking for nuclease inhibitors that can control or stop such activities. The aim is to increase the safety and efficacy of future therapies and to help prevent off-target effects. An international team led by the Helmholtz Institute in Würzburg in cooperation with the University of Freiburg has now applied deep learning for the first time to find natural nuclease inhibitors. The study, published today in the scientific journal "Molecular Cell", identified the first such inhibitor that blocks the activity of Cas13b.

    Bacteria often contain CRISPR-Cas defense systems that protect against viral invaders called phages. In response, phages have evolved proteins that can shut down CRISPR. These are called anti-CRISPR proteins, or Acrs. Researchers believe that there are numerous Acrs that have not yet been discovered. One of those is Chase Beisel, head of the RNA Synthetic Biology Department at the Helmholtz Institute for RNA-based Infection Research (HIRI) in Würzburg, a site of the Helmholtz Centre for Infection Research (HZI) in Braunschweig in cooperation with the Julius-Maximilians-Universität (JMU) Würzburg. "Acrs can be used to better control CRISPR technologies," Beisel says, while acknowledging, "Identifying them means finding a needle in a haystack, since they look nothing like each other." This, he says, has led scientific studies in the past to come up with new prediction tools. However, the success of these methods has been limited, says Beisel. He initiated the study published today in the journal “Molecular Cell”.

    First example of using deep learning for Acr discovery

    Consequently, a team of researchers from the HIRI in Würzburg, together with scientists from the Signalling Research Centres at the University of Freiburg and the Information and Computer Science Department at King Fahd University in Saudi Arabia, has pioneered the use of artificial intelligence to identify new Acrs.

    "Using complex computational learning in combination with a high-throughput screen, we have succeeded in discovering a new anti-CRISPR protein that inhibits the clinically interesting nuclease Cas13b," says Katharina Wandera. The PhD student in Chase Beisel's lab is working on the characterization of Acrs and is a first author of the current paper.

    "The millions of predictions made by our algorithm open up completely new avenues for research," Rolf Backofen from the University of Freiburg is certain. His group developed the method, called DeepAcr, for the study.

    The findings also suggest that DeepAcr can not only be used to discover new proteins that inhibit CRISPR-Cas systems lacking known Acrs. "The identified anti-CRISPR protein AcrVIB1 was not only unknown until now, it also seems to use a completely new mechanism of action," summarizes Omer Alkhnbashi, an assistant professor at King Fahd University who shares the first authorship with Wandera.

    Characterizing this mechanism of action is one of the next steps that will now follow the scientific work.

    The study was supported by funds from the German Research Foundation (DFG) and the Safe Genes Program of the Defense Advanced Research Projects Agency (DARPA).

    This press release is also available on our homepage: https://www.helmholtz-hzi.de/en/news-events/news/view/article/complete/praezisio...

    Helmholtz Centre for Infection Research:
    Scientists at the Helmholtz Centre for Infection Research (HZI) in Braunschweig and its other sites in Germany are engaged in the study of bacterial and viral infections and the body’s defence mechanisms. They have a profound expertise in natural compound research and its exploitation as a valuable source for novel anti-infectives. As member of the Helmholtz Association and the German Center for Infection Research (DZIF) the HZI performs translational research laying the ground for the development of new treatments and vaccines against infectious diseases. http://www.helmholtz-hzi.de/en

    Helmholtz Institute for RNA-based Infection Research:
    The Helmholtz Institute for RNA-based Infection Research (HIRI) was founded in May 2017. It is a joint institution of the Helmholtz Centre for Infection Research (HZI) in Braunschweig and the Julius-Maximilians-Universität Würzburg (JMU). Based on the University hospital campus, the HIRI is the first federal institute to focus on the role of ribonucleic acids (RNAs) in infection processes. Its mission is to combine basic research with the development of new RNA-centric therapeutic approaches to treat infections. http://www.helmholtz-hiri.de

    Contact:
    Dr. Britta Grigull
    Presse & Public Relations
    +49 (0)931-31-81801
    britta.grigull@helmholtz-hiri.de


    Original publication:

    Anti-CRISPR prediction using deep learning reveals an inhibitor of Cas13b nucleases. Wandera KG, Alkhnbashi OS, Bassett HVI, Mitrofanov A, Hauns S, Migur A, Backofen R, Beisel CL (2022). Molecular Cell. DOI: 10.1016/j.molcel.2022.05.003


    Images

    Using complex computational learning in combination with a high-throughput screen, a new anti-CRISPR protein was discovered that inhibits Cas13b.
    Using complex computational learning in combination with a high-throughput screen, a new anti-CRISPR ...
    Chase Beisel
    HIRI/Chase Beisel


    Criteria of this press release:
    Business and commerce, Journalists, Scientists and scholars
    Biology, Chemistry, Medicine
    transregional, national
    Research results
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    Using complex computational learning in combination with a high-throughput screen, a new anti-CRISPR protein was discovered that inhibits Cas13b.


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