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CHUbVi SIGNED

Ubiquitin Chains in Viral Infections

Total Cost €

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EC-Contrib. €

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Partnership

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 CHUbVi project word cloud

Explore the words cloud of the CHUbVi project. It provides you a very rough idea of what is the project "CHUbVi" about.

danger    demonstrating    regulation    diverse    hdac6    agents    interactions    validate    discovery    mechanism    consisting    assays    chemical    tools    immune    gain    synthesis    ebola    threatening    spectrum    reduces    molecular    precise    anti    mers    team    entry    viruses    greatest    life    compounds    proteins    prevalence    models    influenza    utilize    poorly    line    threats    activate    exact    antiviral    unanchored    possibility    human    labeled    biological    tested    offers    blocking    infect    types    infectious    cells    chains    formed    virus    generation    virologist    investigation    broad    particles    aggresome    insights    clear    biochemical    structural    society    dengue    wealth    molecule    evade    ubiquitin    therapies    infections    hosts    implicate    downstream    multidisciplinary    fundamental    infection    despite    biologist    mechanisms    iav    animal    cellular    basis    packaged    nature    health    viral    zika    preventing    mammalian    host    mediators    small   

Project "CHUbVi" data sheet

The following table provides information about the project.

Coordinator
FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION 

Organization address
address: MAULBEERSTRASSE 66
city: BASEL
postcode: 4058
website: www.fmi.ch

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Switzerland [CH]
 Total cost 7˙649˙848 €
 EC max contribution 7˙649˙848 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-SyG
 Funding Scheme ERC-SyG
 Starting year 2020
 Duration (year-month-day) from 2020-03-01   to  2026-02-28

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION CH (BASEL) coordinator 2˙698˙125.00
2    UNIVERSITY OF BRISTOL UK (BRISTOL) participant 2˙785˙048.00
3    EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH CH (ZUERICH) participant 2˙166˙675.00

Map

 Project objective

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.

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The information about "CHUBVI" are provided by the European Opendata Portal: CORDIS opendata.

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