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VIREX SIGNED

Mumps VIRus EXploitation of the human adhesion receptor GPR125

Total Cost €

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EC-Contrib. €

0

Partnership

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 VIREX project word cloud

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

vaccine    fact    assign    herpes    mumps    pox    single    mechanism    7tm    inflammatory    collaborators    appealing    resolution    structural    drug    huge    expertise    generally    gpr125    dna    encoded    functional    painful    seven    central    pneumonia    groundbreaking    caused    tremendous    brain    interference    paramyxoviridae    risk    organ    managed    vaccination    preparation    sh    body    interaction    receptors    pharmacology    expert    perspectives    causes    testis    measles    feasible    modes    clinical    mode    10    rna    symptoms    family    salivary    human    crystal    hydrophobic    neurotropic    amenable    proteins    fear    infections    small    belonging    transmembrane    exceeds    global    economics    nmr    individuals    receptor    pathogen    eliminate    health    infection    cell    hypothesis    gland    action    damage    parts    parotitis    protein    data    vaccinated    programs    virus    virology    viruses    genomes    context    therapeutic    structure    gain    preliminary    interdisciplinary    re    orchitis    half    adhesion   

Project "VIREX" data sheet

The following table provides information about the project.

Coordinator
KOBENHAVNS UNIVERSITET 

Organization address
address: NORREGADE 10
city: KOBENHAVN
postcode: 1165
website: www.ku.dk

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 Denmark [DK]
 Project website https://bmi.ku.dk/english/research/molpharm/mettemrosenkilde/
 Total cost 1˙813˙367 €
 EC max contribution 1˙813˙367 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-CoG
 Funding Scheme ERC-COG
 Starting year 2016
 Duration (year-month-day) from 2016-07-01   to  2021-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KOBENHAVNS UNIVERSITET DK (KOBENHAVN) coordinator 1˙813˙367.00

Map

 Project objective

Mumps virus is a re-emerging pathogen that causes painful inflammatory symptoms, such as parotitis (salivary gland infection) and orchitis (testis infection). It is highly neurotropic with evidence of brain infection in half of cases and clinical evidence in up to 10%. It is a small RNA virus belonging to the family of paramyxoviridae that includes e.g. viruses for measles and pneumonia, all having a huge impact on global economics and human health. Current vaccine programs have not managed to eliminate mumps and infections occur also in vaccinated individuals. Seven transmembrane (7TM) receptors are important drug targets. Large DNA viruses (herpes- and pox-) assign large parts of their genomes to exploit 7TM receptors. No such mechanism has however yet been described for small viruses. Based on strong preliminary data, I will in this interdisciplinary project test the groundbreaking hypothesis that the adhesion 7TM receptor GPR125 is central for the organ damage caused by mumps virus via an interaction with the mumps virus-encoded short-hydrophobic (SH)-protein. I will do so by determining: 1 - The functional consequences of GPR125-SH-interaction at a single cell, organ and whole body level within the context of mumps virus infection 2 - The structural requirements for the GPR125-mumps virus interaction using NMR and resolution of crystal structure in preparation for future drug design The project is high risk and high gain, yet the gain clearly exceeds the risk. On account of my past expertise in pharmacology and virology, and that of several expert collaborators, the project is indeed feasible. It has tremendous perspectives as SH-proteins are present also in other viruses. The SH-GPR125 complex might thus represent a general principle for organ damage and a mode of action more generally amenable to therapeutic interference. In fact, novel approaches, mechanism-based, might be seen as more appealing to those who fear current vaccination 'modes'.

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

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