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NanoMechShape SIGNED

Molecular control of actin network architecture and mechanics during cell shape changes

Total Cost €

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EC-Contrib. €

0

Partnership

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 NanoMechShape project word cloud

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

systematically    thin    crosstalk    regulatory    actin    spreading    rounded    explore    paving    super    networks    nanomechshape    principles    first    membrane    architecture    interdisciplinary    comprise    investigations    integrating    ingression    unveil    cell    pathologies    morphogenesis    fundamental    establishment    gap    shape    physiology    elusive    animal    mechanisms    cortical    nanoscale    difficulty    embryonic    transitions    regulation    driving    lamellipodia    cells    heart    precise    fall    regulated    morphology    fate    contractions    determinants    mouse    behaviors    primary    truly    molecular    biology    cortex    differentiation    underlying    physics    ing    understand    gradient    exemplar    bridging    multidisciplinary    architectural    forces    deformations    tension    mitosis    filopodia    furrow    microscopy    stem    deregulation    organisation    resolution    categories    contractile    compare    network    probing    electron    cytokinetic   

Project "NanoMechShape" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.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 1˙943˙071 €
 EC max contribution 1˙943˙071 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-COG
 Funding Scheme ERC-COG
 Starting year 2019
 Duration (year-month-day) from 2019-05-01   to  2024-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 1˙943˙071.00

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 Project objective

Precise control of shape is key to cell physiology, and cell shape deregulation is at the heart of many pathologies. As cell morphology is controlled by forces, studies integrating physics with biology are required to truly understand morphogenesis. NanoMechShape will take such an interdisciplinary approach to investigate the regulation of animal cell shape. In animal cells, actin networks are the primary determinants of shape. Most cell shape changes fall into two categories: 1) those driven by contractions of the actin cortex, a thin network underlying the membrane in rounded cells; and 2) those resulting from transitions between the cortex and other actin networks, such as lamellipodia and filopodia. To understand cell deformations, it is thus essential to understand the regulation of cortex contractile tension and the mechanisms controlling transitions in actin architecture. NanoMechShape will comprise three aims. First, we will explore how cortex tension is regulated. We will focus on the role of cortex architecture, which remains elusive due to the difficulty in probing the organisation of the thin cortical network. We will unveil cortex architecture using super-resolution and electron microscopy, and systematically investigate how nanoscale architectural features affect tension. Second, we will explore how the identified regulatory mechanisms contribute to the establishment of a cortical tension gradient. We will focus on the gradient driving cytokinetic furrow ingression, an exemplar tension-driven shape change. Third, we will investigate transitions in actin architecture underlying cell spreading. We will compare spreading at the end of mitosis and during differentiation of mouse embryonic stem cells, paving the way to investigations of the crosstalk between cell shape and fate. By bridging a fundamental gap between molecular processes and cell-scale behaviors, our multidisciplinary study will unveil some of the fundamental principles of cell morphogenesis.

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

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