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FUSEDESIGN SIGNED

Model-guided design of a stabilized pre-fusion class III viral fusogen, rabies virus glycoprotein

Total Cost €

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EC-Contrib. €

0

Partnership

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 FUSEDESIGN project word cloud

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

generation    vaccinology    combination    unusual    mutants    expressed    combining    antiviral    spanning    class    forms    truly    molecular    immunogens    data    vaccines    training    skill    mutations    contribution    host    public    translational    homology    reported    guide    discipline    structural    world    designed    fellowship    people    stabilization    kills    prohibitively    55    cutting    structures    biology    form    vaccine    trimeric    biochemistry    animals    costly    conserved    receptors    quality    glycoprotein    demand    neutralizing    insights    stabilise    protein    interaction    interventions    immunologically    cells    post    equip    billions    antigenically    certain    human    guided    mouse    clinically    fusogens    subunit    departments    enveloped    viruses    computational    fusion    structure    pathogens    antibodies    models    rabies    academic    stabilize    critical    fatal    exposure    centre    structurally    cumbersome    mammalian    virus    stability    model    position    health    fusogen    herpesvirus    notably    stabilized    edge    rvg    glycoproteins    candidates    transiently    tractable    immunology    researcher    herpesviruses   

Project "FUSEDESIGN" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD 

Organization address
address: WELLINGTON SQUARE UNIVERSITY OFFICES
city: OXFORD
postcode: OX1 2JD
website: www.ox.ac.uk

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 United Kingdom [UK]
 Total cost 224˙933 €
 EC max contribution 224˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-07-01   to  2021-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD UK (OXFORD) coordinator 224˙933.00

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 Project objective

This proposal aims to stabilize the pre-fusion form of rabies virus glycoprotein (RVG), the most structurally-tractable clinically-relevant class III fusogen by combining computational biology, immunology, and structural biology. Rabies virus is fatal; it kills 55,000 people each year and costs billions to control it in animals. Current human rabies vaccines are cumbersome to use and prohibitively costly, thus there is demand for a new generation of rabies vaccines. Enveloped viruses’ fusion glycoproteins are important subunit vaccine candidates. Structure-guided stabilization of class I fusogens has been a major advance in vaccinology. Many major human pathogens have class III fusogens (notably, all herpesviruses and rabies virus): several post-fusion structures have been reported, but their antigenically critical pre-fusion forms have not been stabilized. A high-quality homology model of RVG will guide design of mutations to stabilise the trimeric pre-fusion protein. Designed mutants will be transiently expressed in mammalian cells, selected for stability, and characterized immunologically. Lead candidates will be used as immunogens in mouse models and in structural studies. These data will guide design of improved rabies vaccines, and provide insights into RVG’s interaction with neutralizing antibodies and host receptors. Certain structural elements are conserved across class III fusogens, and so the approach may lead towards stabilization of herpesvirus fusogens. The fellowship will be based between two departments at a world-class host institution. Together, they will offer the Researcher an unusual combination of exposure to both cutting-edge molecular biochemistry and Europe’s leading academic centre for translational vaccine development. This unique training will equip the Researcher with a truly discipline-spanning skill set and position her to make a leading contribution to the development of novel antiviral interventions and public health.

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