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ArpComplexity SIGNED

Defining the role of Arp2/3 complex diversity at multiple scales of biology

Total Cost €

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EC-Contrib. €

0

Partnership

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 ArpComplexity project word cloud

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individual    dynamic    function    molecular    molecule    composition    encoded    stability    cells    subunit    gain    vitro    cell    humans    tomography    takes    live    array    imaging    contribution    genetically    sustainability    myofibers    operation    interdisciplinary    advantage    consisting    entity    critical    gomes    dramatically    members    labs    variations    subunits    single    structure    cellular    microscopy    risk    mammals    diversification    strengths    eight    physiological    physiology    actin    basis    protein    complexes    stimulate    isoform    transgenic    branched    hierarchies    biological    electron    expressing    networks    builds    purified    diversity    family    biology    mice    seven    arp2    muscle    plan    modified    reveal    influence    quantitative    lab    complexity    contributes    perform    always    synergistic    powerful    cytoskeleton    dependence    cultured    multiple    human    cryo    functional    cryoelectron    developmental    scales    reagents    structural    body    fluorescence    shown    model    isoforms   

Project "ArpComplexity" data sheet

The following table provides information about the project.

Coordinator
THE FRANCIS CRICK INSTITUTE LIMITED 

Organization address
address: 1 MIDLAND ROAD
city: LONDON
postcode: NW1 1AT
website: www.crick.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 10˙715˙153 €
 EC max contribution 10˙715˙153 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-SyG
 Funding Scheme ERC-SyG
 Starting year 2019
 Duration (year-month-day) from 2019-07-01   to  2025-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE FRANCIS CRICK INSTITUTE LIMITED UK (LONDON) coordinator 4˙148˙087.00
2    BIRKBECK COLLEGE - UNIVERSITY OF LONDON UK (LONDON) participant 3˙359˙131.00
3    INSTITUTO DE MEDICINA MOLECULAR JOAO LOBO ANTUNES PT (LISBOA) participant 3˙207˙935.00

Map

 Project objective

The actin cytoskeleton of the cell is critical for the complex, integrated processes associated with development, operation and sustainability of the human body. The Arp2/3 complex consisting of seven protein subunits is essential to stimulate dynamic branched actin networks needed for multiple cellular processes. The Arp2/3 complex has always been considered as a single entity, but in humans and other mammals, three of the Arp2/3 complex subunits are encoded by two isoforms, thus allowing the formation of eight distinct Arp2/3 complexes. The Way lab has shown that Arp2/3 subunit composition dramatically affects the formation and stability of branched actin networks. The Way and Gomes labs have shown how specific Arp2/3 isoforms are essential for muscle development.

Our synergistic, high-risk, high-gain goal is to define the role of Arp2/3 complex diversity at three hierarchies of biology:

1. Molecular basis of Arp2/3 diversification With purified isoform-specific complexes we will perform cryo-electron microscopy and single molecule fluorescence microscopy to reveal the structural variations and influence of Arp2/3 diversity on actin networks in vitro.

2. Cellular function of different Arp2/3 complexes With cells expressing specific Arp2/3 isoforms, we will use quantitative live cell imaging and cryoelectron tomography to reveal the dependence of cellular actin networks on Arp2/3 diversity and its functional consequences.

3. Developmental and physiological role of individual Arp2/3 complexes. With genetically modified cultured myofibers and transgenic mice, we will use an array of imaging approaches to reveal the contribution of different Arp2/3 family members to muscle development, structure and physiology.

Our interdisciplinary plan builds on the strengths of our three labs, takes advantage of unique reagents and powerful model systems, and will allow us to determine how Arp2/3 diversity contributes to biological complexity at multiple scales.

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

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