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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.

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

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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