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MicroMISTRANS SIGNED

Error-prone protein synthesis in fungal pathogens Microsporidia: its scope and potential therapeutic targeting

Total Cost €

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EC-Contrib. €

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Partnership

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 MicroMISTRANS project word cloud

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

young    prone    interactions    excellent    microbiology    genes    first    industrially    mammalian    tools    evolution    biochemistry    move    uk    synergistically    organisms    modulate    expertise    evade    transition    appropriate    eukaryotic    drugs    insights    mistranslation    industrmicrosporidia    pathogens    translation    cell    health    grow    newcastle    implications    outcome    world    combining    microsporidia    proteomics    ubiquitous    cultivating    toxicity    equip    threaten    fish    university    skill    intracellular    protein    asset    cultures    background    investigation    laboratories    unexplored    renowned    manipulating    training    biology    molecular    completing    inaccurate    career    host    synthesis    valuable    lines    handful    lack    genetic    scientist    independent    proteomes    error    multidisciplinary    myriad    manipulate    cattle    insects    poorly    treatable    center    diversify    rare    pathogen    totally    laboratory    obligate    despite    researcher    immune    human    complement    proteomic    infected    experimental    isoforms    transferable   

Project "MicroMISTRANS" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF NEWCASTLE UPON TYNE 

Organization address
address: KINGS GATE
city: NEWCASTLE UPON TYNE
postcode: NE1 7RU
website: http://www.ncl.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-2019
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2020
 Duration (year-month-day) from 2020-03-01   to  2022-02-28

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF NEWCASTLE UPON TYNE UK (NEWCASTLE UPON TYNE) coordinator 224˙933.00

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 Project objective

Microsporidia are ubiquitous and poorly treatable eukaryotic obligate intracellular pathogens that threaten human health and industrMicrosporidia are poorly treatable eukaryotic pathogens that threaten human health and industrially valuable insects, fish, and cattle. Despite Microsporidia being recognized as emerging pathogens that require development of new drugs, many aspects of their biology remain totally unexplored due to a lack of appropriate genetic tools and because only a handful of laboratories in the world can grow and manipulate Microsporidia in infected host organisms or cell cultures. This proposal involves a promising scientist with a background in biochemistry and molecular biology and who will move to a host laboratory in Newcastle University, UK – a renowned center for excellent training of young researchers, and a leading research center in the field of pathogen evolution. The researcher will undertake a multidisciplinary investigation, combining microbiology, proteomics, and molecular biology, in order to investigate how Microsporidia diversify their proteomes through error-prone protein synthesis (mistranslation). The researcher’s training at the host laboratory – in cultivating and manipulating Microsporidia in mammalian cell lines for proteomic and toxicity studies – will synergistically complement the researcher’s expertise in molecular biology of protein synthesis. Completing the project will equip the researcher with a rare, increasingly valuable and transferable skill of Microsporidia experimental biology that will be a key asset in his transition to an independent research career. The project will deliver the first detailed insights into the ability of Microsporidia to produce myriad protein isoforms from their genes as a result of highly inaccurate translation. The outcome of this project will have general implications for understanding how eukaryotic pathogens can modulate their interactions with the host and evade host immune systems.

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