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Ubiquitin Chains in Viral Infections

Descrizione del progetto

Decifrare i meccanismi del processo di infezione virale

I meccanismi molecolari dell’infezione virale e dell’evasione del sistema immunitario negli ospiti mammiferi restano scarsamente compresi. Il progetto CHUbVi, finanziato dall’UE, identificherà i percorsi implicati nel processo di infezione, con l’obiettivo di fornire target molecolari per composti antivirali ad ampio spettro. I precedenti studi del team hanno osservato che l’istone deacetilasi 6 e le catene di ubiquitina non ancorate agiscono come mediatori chiave dell’ingresso virale attraverso il percorso di elaborazione dell’aggresoma che organizza le proteine mal ripiegate in posizioni particolari, quando il sistema di degradazione delle proteine della cellula è sopraffatto. Studi dettagliati sul coinvolgimento di questo percorso consentiranno lo sviluppo di saggi biochimici e cellulari per l’infezione da influenza A, nonché la ricerca relativa a se questo percorso sia correlato o meno al processo di infezione di altri virus tra cui Zika, dengue, Ebola e MERS.

Obiettivo

Viruses such as Influenza A (IAV) and others remain one of the greatest threats to human health and society. Despite their danger and widespread prevalence, the molecular mechanisms of how they infect mammalian hosts and evade the immune system remains poorly understood. Recent studies from our team implicate two common proteins – HDAC6 and unanchored ubiquitin chains – in host cells as key mediators of viral entry via the aggresome processing pathway. This discovery offers a new line of investigation for understanding and preventing viral infections.

By identifying the pathways and interactions involved in this infection process, we will provide new molecular targets for the development of broad-spectrum antiviral compounds. Multidisciplinary studies by a team consisting of a molecular biologist, a virologist, and a chemical biologist will use a diverse set of tools to validate these pathways and gain fundamental knowledge about their regulation. To achieve this, detailed studies on the exact nature of the ubiquitin chains needed to activate HDAC6 will allow the development of biochemical and cellular assays of Influenza A infection and enable the determination of the precise mechanism and the downstream cellular pathways necessary for viral infection. The chemical synthesis of labeled ubiquitin chains will support detailed structural studies and a clear understanding of how they are formed and packaged into infectious viral particles. The strong possibility that numerous other virus types also utilize this pathway will be tested with life-threatening agents of current concern including Zika, Dengue, Ebola, and MERS viruses.

By demonstrating – with both biological approaches and small molecule compounds – that blocking these cellular processes in cells and animal models reduces viral infection, this project will provide a wealth a novel insights and the basis for the development of a new generation of anti-viral therapies.

Meccanismo di finanziamento

ERC-SyG - Synergy grant

Istituzione ospitante

FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION
Contribution nette de l'UE
€ 2 698 125,00
Indirizzo
FABRIKSTRASSE 2
4056 BASEL
Svizzera

Mostra sulla mappa

Regione
Schweiz/Suisse/Svizzera Nordwestschweiz Basel-Stadt
Tipo di attività
Research Organisations
Collegamenti
Costo totale
€ 2 698 125,00

Beneficiari (3)