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Viral RNA-methyltransferases: function, structure and inhibition

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F24%3A00604159" target="_blank" >RIV/61388963:_____/24:00604159 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.xray.cz/setkani/abst2024/784.htm" target="_blank" >https://www.xray.cz/setkani/abst2024/784.htm</a>

  • DOI - Digital Object Identifier

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Viral RNA-methyltransferases: function, structure and inhibition

  • Popis výsledku v původním jazyce

    Methyltransferases (MTases) associated with coronaviruses, such as nsp10/16 and nsp14, are responsible for the final stages of RNA-cap formation within the cytoplasm. This cap is crucial for maintaining the stability of viral RNA and plays a pivotal role in evading the innate immune response. Uncapped RNA is swiftly detected by the innate immune system, triggering degradation and activating antiviral defenses. Consequently, the coronaviral MTases have become focal points of extensive scientific investigation. Recently, through the use of X-ray and cryo-electron microscopy techniques, the structures of both enzymes have been elucidated, even in complex with other components of the viral replication machinery. The application of high-throughput screening methods and the design of inhibitors guided by structural insights have resulted in the identification of potent inhibitors targeting these MTases. This talk critically examines the remarkable progress made in the field of coronaviral MTases since the onset of the COVID-19 pandemic. Additionally, it is worth noting that similar investigations into poxviruses' MTases have also contributed significantly to our understanding of viral replication and immune evasion strategies.

  • Název v anglickém jazyce

    Viral RNA-methyltransferases: function, structure and inhibition

  • Popis výsledku anglicky

    Methyltransferases (MTases) associated with coronaviruses, such as nsp10/16 and nsp14, are responsible for the final stages of RNA-cap formation within the cytoplasm. This cap is crucial for maintaining the stability of viral RNA and plays a pivotal role in evading the innate immune response. Uncapped RNA is swiftly detected by the innate immune system, triggering degradation and activating antiviral defenses. Consequently, the coronaviral MTases have become focal points of extensive scientific investigation. Recently, through the use of X-ray and cryo-electron microscopy techniques, the structures of both enzymes have been elucidated, even in complex with other components of the viral replication machinery. The application of high-throughput screening methods and the design of inhibitors guided by structural insights have resulted in the identification of potent inhibitors targeting these MTases. This talk critically examines the remarkable progress made in the field of coronaviral MTases since the onset of the COVID-19 pandemic. Additionally, it is worth noting that similar investigations into poxviruses' MTases have also contributed significantly to our understanding of viral replication and immune evasion strategies.

Klasifikace

  • Druh

    O - Ostatní výsledky

  • CEP obor

  • OECD FORD obor

    10608 - Biochemistry and molecular biology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/LX22NPO5103" target="_blank" >LX22NPO5103: Národní institut virologie a bakteriologie</a><br>

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2024

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů