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A structural and functional understanding Influenza virus mRNA production in the context of the transcriptionally functional ribonucleoprotein (RNP) particle.

Descrizione del progetto

Un complesso della proteina RNA fondamentale per la trascrizione dell’influenza

I virus dell’influenza sono virus a base di RNA che rappresentano una grande minaccia per la salute umana attraverso epidemie annuali e occasionali pandemie. Comprendere la biologia dei virus influenzali è fondamentale per la progettazione di farmaci e vaccini antivirali. Il progetto Influenza RNP, finanziato dall’UE, approfondirà i complessi ribonucleoproteici coinvolti nella trascrizione dell’RNA genomico virale in mRNA. I ricercatori mirano a delineare i cambiamenti dinamici che si verificano nella struttura dei complessi ribonucleoproteici durante la trascrizione. I risultati forniranno informazioni molecolari e biochimiche fondamentali sui meccanismi di replicazione dei virus dell’influenza, aprendo nuove strade per la ricerca farmaceutica anti-influenzale. Inoltre, i metodi sviluppati possono essere applicati per studiare i complessi ribonucleoproteici essenziali di altri virus RNA patogeni.

Obiettivo

Influenza is a major public health burden, with seasonal outbreaks contributing significantly to mortality worldwide, and the emergence of pandemic strains remaining an ever-present threat. Influenza drug and vaccine conception efforts are aided by a thorough understanding of its molecular biology.

A key aspect of the influenza lifecycle is the production of capped and poly-adenylated messenger RNA by the heterotrimeric influenza polymerase (FluPol). Ground-breaking work performed by the Cusack lab, has described with residue-resolution detail, the FluPol structures that form during transcription of short, non-nucleoprotein (NP) bound viral RNAs (vRNAs). However, influenza transcription in vivo occurs within the ribonucleoprotein (RNP) particle and does not utilise naked genome segments. The viral RNP (vRNP) is a super-helical complex composed FluPol bound at the conserved 3′ and 5′ ends of a vRNA, which is coated with NP. The current low-resolution structures provide little information about the molecular details of vRNP function, particularly, how NPs interact with FluPol and the vRNA template.

Via an inter-disciplinary approach, I will utilise cryo-electron microscopy methods, transcription assays and single-molecule fluorescence, to obtain the first high resolution structure of a dynamic influenza vRNP, with a particular focus on the spatial organisation of NPs relative to FluPol. In addition to this work facilitating future influenza drug research, it will provide a basis to investigate the vRNP during other lifecycle stages and act as proof-of-principle for study of other viral protein-RNA complexes, such as those from corona-, arena- and bunyaviruses.

Work will be performed in the groups of Stephen Cusack and Olivier Duss based at EMBL Grenoble and Heidelberg, respectively. Here, I will have access to world-leading facilities and training opportunities, supporting my growth as an independent researcher and an expert in RNA virus structural biology.

Campo scientifico (EuroSciVoc)

CORDIS classifica i progetti con EuroSciVoc, una tassonomia multilingue dei campi scientifici, attraverso un processo semi-automatico basato su tecniche NLP.

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Coordinatore

EUROPEAN MOLECULAR BIOLOGY LABORATORY
Contribution nette de l'UE
€ 184 707,84
Indirizzo
Meyerhofstrasse 1
69117 Heidelberg
Germania

Mostra sulla mappa

Regione
Baden-Württemberg Karlsruhe Heidelberg, Stadtkreis
Tipo di attività
Research Organisations
Collegamenti
Costo totale
€ 184 707,84