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Getting to grips with AAA+ ATPases encoded by positive-strand RNA viruses

Project description

How viral enzymes drive infection and persistence

Noroviruses and enteroviruses are everywhere. They sweep through crowded spaces such as schools and offices, spreading fast and infecting millions each year. Even though they are among the world’s leading causes of gastrointestinal and respiratory illness, key gaps remain in scientific understanding. Researchers know that both virus families rely on the same enzyme to replicate inside human cells, but how it functions remains unclear. The ERC-funded PicAAA project aims to use advanced imaging and molecular tools to uncover how the enzyme works. This knowledge could strengthen efforts to prevent and control future outbreaks.

Objective

Noroviruses (NoVs) and enteroviruses (EVs) cause numerous gastrointestinal and respiratory infections. Their contagious nature and high mutation rates can lead to the emergence of new pathogenic strains. Understanding these viruses is crucial for controlling outbreaks and to maintain global health. Both NoVs and EVs are members of the order Picornavirales and share commonalities in their replication strategies. Their positive-strand RNA genomes encode non-structural proteins (NSPs) that exploit host cells to create membranous replication organelles for genome replication and virion formation. The most enigmatic NSP encoded by these viruses is a AAA+ ATPase (NoV NS3 and EV 2C). These enzymes have many proposed roles in the virus lifecycle, such as RNA helicase/chaperone activity, membrane rearrangement, and genome encapsidation. However, their structure and the molecular basis for their diverse activities are poorly understood due to challenges in producing stable and soluble complexes for structural analysis and the lack of tools to accurately visualize NSPs in a cellular context. Drawing from my decade-long experience in structural virology and recent success in engineering soluble AAA+ ATPases, I aim to unravel the multiple functions of NoV NS3 and EV 2C. Specifically, I will: 1) Decipher the structure-function relationship of these enzymes through single-particle cryo-electron microscopy analysis of the nucleotide and RNA-bound complexes. 2) Create a toolkit of small molecules and nanobodies to investigate the functional sites in NS3. 3) Utilize cryo-electron tomography to visualise NS3 and 2C in infected cells, guided by genetically encoded tags developed in this project. Collectively, the results of this project will provide new mechanistic insights into the functions that NoV and EV AAA+ ATPases carry out during the viral lifecycle and pave the way for the development of novel antiviral compounds capable of inhibiting these functionally indispensable enzymes.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

(opens in new window) ERC-2024-STG

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Host institution

UNIVERSITEIT UTRECHT
Net EU contribution
€ 1 550 000,00
Address
HEIDELBERGLAAN 8
3584 CS Utrecht
Netherlands
Activity type
Higher or Secondary Education Establishments
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Total cost
€ 1 550 000,00

Beneficiaries (1)