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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.

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

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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