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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.

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

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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