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MICROCRYO SIGNED

Microsystems for Cryomicroscopy

Total Cost €

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EC-Contrib. €

0

Partnership

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 MICROCRYO project word cloud

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

reversible    reversibility    emerged    vitrification    instrumentation    dynamic    microscopy    technologies    elucidate    decade    synergy    cryo    optics    powerful    limitations    molecular    organisms    unperturbed    systematically    resume    spatial    trafficking    model    cells    resolution    cooling    cryogenic    despite    cellular    preparation    events    proteins    direct    transport    division    untapped    imaging    ultra    ultimately    sophisticated    cryofixation    basis    electron    stem    heating    millisecond    rapid    extremely    class    1960s    single    resolved    temporal    imaged    membrane    warming    synaptic    create    microfluidic    sperm    incrementally    revealing    revolutionize    biological    transmission    nanometer    combined    infancy    fast    cell    function    reversed    light    structure    time    modes    temperature    oocytes    structural    progress    context    ultrastructural    live    breakthroughs    cryopreservation    microscope    first    dynamics    small    microsystems   

Project "MICROCRYO" data sheet

The following table provides information about the project.

Coordinator
TECHNISCHE UNIVERSITAT DARMSTADT 

Organization address
address: KAROLINENPLATZ 5
city: DARMSTADT
postcode: 64289
website: www.tu-darmstadt.de

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 Germany [DE]
 Total cost 1˙994˙562 €
 EC max contribution 1˙994˙562 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-COG
 Funding Scheme ERC-COG
 Starting year 2019
 Duration (year-month-day) from 2019-02-01   to  2024-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    TECHNISCHE UNIVERSITAT DARMSTADT DE (DARMSTADT) coordinator 1˙994˙562.00
2    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (MUENCHEN) participant 0.00

Map

 Project objective

This proposal aims to revolutionize time-resolved light and electron cryo-microscopy of fast cellular dynamics using a new class of cryogenic microsystems for the reversible cryofixation of cells and small model organisms by ultra-rapid cooling. This will contribute to our understanding of biological structure and function by revealing the dynamics of specific proteins in the ultrastructural context of a cell at nanometer spatial and millisecond temporal resolution.

Despite rapid progress in the field, much of the potential of microscopy at cryogenic temperature today is still untapped due to limitations in methods and instrumentation for sample preparation. First, vitrification technologies for cryo-microscopy have evolved only incrementally since the 1960s and cannot be combined with many of the sophisticated live imaging methods that have emerged over the past decade. Second, while the synergy of light and electron cryo-microscopy is extremely powerful, cryo-microscopy with light is still in its infancy. Finally, new technologies for ultra-rapid heating and cooling of single cells are needed to systematically advance our understanding of reversibility in the cryopreservation of e.g. stem cells, oocytes, or sperm cells. Here I propose to create a microfluidic technology for the direct vitrification of cells in the light microscope by ultra-rapid cooling with millisecond time resolution. The cells will then be imaged at high resolution using electron microscopy and advanced modes of light microscopy combined with new optics adapted to cryogenic conditions. Ultimately, we will elucidate if and under which conditions cryofixation can be reversed by ultra-rapid warming such that dynamic cellular processes resume unperturbed.

We expect that the research proposed here will enable breakthroughs in understanding the structural and molecular basis of fast cellular events including transport, membrane trafficking, cell division, and synaptic transmission.

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

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