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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.

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

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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