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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

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

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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