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RhoSNATCH SIGNED

Dissecting Rho GTPase signalling networks through acute perturbation techniques

Total Cost €

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EC-Contrib. €

0

Partnership

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 RhoSNATCH project word cloud

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

give    live    identification    power    patterns    reversible    spatiotemporally    micrometer    genome    editing    fibroblast    acutely    fibroblasts    rho    maintains    signaling    recorded    living    models    vision    timescales    microfluidic    outputs    technologies    led    extension    precise    questions    combination    imaging    discovered    subset    output    downstream    rac1    edge    image    biologically    perturbed    experiments    assisted    molecular    migration    crosstalk    rhoa    modules    time    data    activation    positions    zones    complexes    dissect    rhosnatch    first    gtpase    recent    cytoskeletal    perturbing    complexity    single    endogenous    cdc42    newly    circuitry    computer    regulate    upstream    spatiotemporal    cell    length    fluctuate    dynamics    fine    gtpases    scales    space    tune    functional    motile    multiplexing    subminute    insights    networks    multiple    induce    cells    recording    regulators    functions    perturb    unprecedented    tunes    dimerizing    resolution    systematically    chemical   

Project "RhoSNATCH" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAET BERN 

Organization address
address: HOCHSCHULSTRASSE 6
city: BERN
postcode: 3012
website: http://www.unibe.ch

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 Switzerland [CH]
 Project website https://www.pertzlab.net/cell-motility-and-cytoskeleton
 Total cost 187˙419 €
 EC max contribution 187˙419 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2016
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-04-01   to  2019-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAET BERN CH (BERN) coordinator 187˙419.00

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 Project objective

Recent advances in technologies to measure Rho GTPase signaling with unprecedented spatiotemporal resolution in single living cells have led to novel questions. Important new insights are that Rho GTPase signaling involves the formation of signaling complexes that fluctuate on subminute time and micrometer length scales, and that complex signaling networks involving multiple Rho GTPases fine tune the leading edge dynamics that power fibroblast migration. Novel methodologies are required to dissect this newly discovered signaling complexity. RhoSNATCH aims to characterize these signaling networks by acutely perturbing and recording Rho GTPase signaling at biologically relevant timescales in live-cell imaging experiments of cell migration. I will identify the crosstalk between Rac1/RhoA/Cdc42 that positions and maintains specific Rho GTPase activity zones in time and space and identify dedicated functional signaling modules that fine tune specific cytoskeletal output at the leading edge of motile fibroblasts. Microfluidic technology will be used to induce precise fibroblast leading edge signaling states. Genome editing in combination with a reversible chemical dimerizing system will be used to acutely perturb endogenous RhoA,Cdc42 and Rac1 signaling, as well as a subset of their upstream regulators that regulate leading edge dynamics. Rho GTPase activation patterns and downstream cytoskeletal outputs will be systematically recorded in the different perturbed states. Computer-vision assisted image analysis will allow the multiplexing of multiple data sets to produce one of the first integrated models of the molecular circuitry that fine-tunes Rho GTPase signaling and cytoskeletal dynamics during leading edge extension. This novel, integrated approach will allow for the first time the identification of different spatiotemporally organised Rho GTPase signaling modules, and give relevant insight into the crosstalk between and functions of Rho GTPases in time and space.

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

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