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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.

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

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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