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MitoQuant SIGNED

Development of Deep-UV Quantitative Microscopy for the Study of Mitochondrial Dysfunction

Total Cost €

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EC-Contrib. €

0

Partnership

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 MitoQuant project word cloud

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

wavelengths    network    strives    learning    cellular    crispr    specificity    continued    adds    possibility    sequences    autofluorescence    mitochondria    deductions    first    extract    image    editor    vital    excellent    presented    illumination    transfection    proteins    reconstruction    100nm    experiments    hence    microscopy    trained    fluorescent    routines    classify    microscopes    fluorescently    skews    track    de    techniques    material    start    surprising    light    turn    resolution    employ    highest    contrast    building    mitochondrial    time    overexpression    levels    noising    neural    fluorescence    uv    microscope    mitoquant    deep    concurrently    cas9    modifies    gene    labelled    reduces    circumvents    neurodegeneration    little    dysfunction    machinery    linked    algorithms    diseases    interplay    quantitative    cell    overshadowing    live    organelles    researcher    numerical    signal    play    sparse    optics    simultaneously    label    record    diabetes    compiled    issue    signals    quality    contextual    machine    free    apertures    suited    technique    counter    imaging    dna    worry    good    superresolution    originally    instrument    molecular    establishing    science    matching    dynamics    structured   

Project "MitoQuant" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITETET I TROMSOE - NORGES ARKTISKE UNIVERSITET 

Organization address
address: HANSINE HANSENS VEG 14
city: TROMSO
postcode: 9019
website: http://uit.no/

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 Norway [NO]
 Total cost 202˙158 €
 EC max contribution 202˙158 € (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    UNIVERSITETET I TROMSOE - NORGES ARKTISKE UNIVERSITET NO (TROMSO) coordinator 202˙158.00

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 Project objective

Mitochondria play a vital role in the cellular machinery, hence it is little surprising that their dysfunction has been linked to many diseases, from diabetes to neurodegeneration. However, as many studies on the interplay of organelles and molecular dynamics often employ fluorescence microscopy, a continued worry overshadowing findings and deductions is the possibility that the transfection-induced overexpression of fluorescent proteins skews the obtained results. A recent approach, the gene editor CRISPR-CAS9, which modifies rather than adds DNA sequences, circumvents this issue, but in turn often reduces the available signal levels. To counter low signals and yet offer highest resolution and specificity, MitoQuant aims to image contextual mitochondrial information with label-free superresolution, while simultaneously enhance image quality of specific but sparse fluorescently labelled proteins of interest through recently presented de-noising routines based on machine learning. Therefore, the development of a novel instrument to provide adequate resolution and contrast, matching label-based live-cell superresolution techniques like structured illumination microscopy, is the first main goal of this project. The proposed microscope will work in the deep UV range and employ dedicated optics originally developed for material science to provide high numerical apertures at short wavelengths, thus enabling live-cell imaging in the 100nm range. Concurrently, a neural network will be compiled and trained to enhance signals under low-light conditions and to extract and classify cellular organelles based on their quantitative phase and autofluorescence information. Building on an excellent track record of developing application-tailored microscopes as well as advanced image reconstruction and processing algorithms particularly suited for live-cell superresolution, the researcher strives to start with first live-cell experiments in good time after establishing the technique.

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The information about "MITOQUANT" are provided by the European Opendata Portal: CORDIS opendata.

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