Opendata, web and dolomites

CRYTOCOP SIGNED

Coat assembly and membrane remodelling: understanding regulation of protein secretion

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 CRYTOCOP project word cloud

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

compartments    view    perspectives    lab    complexes    subtomogram    tomography    bilayer    uniquely    form    shapes    variety    carry    tackle    chemical    accommodate    these    fast    membrane    capture    couple    characterise    assembled    regulated    deformation    mediate    cell    proteins    techniques    assembles    structures    assembly    complexity    vitro    membranes    trafficking    characterised    answer    concentric    molecular    transport    cargoes    ranging    er    regulatory    vesicles    export    newly    regulation    mediates    outstanding    assemble    light    layers    understand    ill    spherical    functions    protein    functional    eukaryotic    copii    manner    identities    sizes    relationship    electron    resolutions    cells    tubules    combination    placed    synthesized    structural    shape    obtain    material    flexibility    complete    reconstitutions    forefront    interactions    exemplified    questions    carriers    coat    cargo    architecture    shed    bound    averaging    cryo    vesicular    components    perfectly    exchange   

Project "CRYTOCOP" data sheet

The following table provides information about the project.

Coordinator
BIRKBECK COLLEGE - UNIVERSITY OF LONDON 

Organization address
address: MALET STREET
city: LONDON
postcode: WC1E 7HX
website: www.bbk.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˙499˙175 €
 EC max contribution 1˙499˙175 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-11-01   to  2024-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    BIRKBECK COLLEGE - UNIVERSITY OF LONDON UK (LONDON) coordinator 1˙499˙175.00

Map

 Project objective

Eukaryotic cells are organised in membrane-bound compartments, which have defined chemical identities and carry out specific essential functions. Exchange of material between these compartments is necessary to maintain cell functionality, and is achieved in a highly specific and regulated manner by vesicular transport. To mediate protein trafficking, coat complexes assemble on membranes and couple bilayer deformation with cargo capture into transport carriers. How coat assembly can deliver the flexibility necessary to accommodate a wide variety of cargo proteins, and how the process can be regulated, are outstanding questions in the field. This is exemplified by the COPII coat, which mediates export from the ER of about a third of newly synthesized proteins. COPII assembles into two concentric layers and can form transport carriers of a variety of shapes and sizes, including tubules and spherical vesicles. This is important for export of large cargoes and is a process targeted by cargo-specific regulatory factors. The aim of this project proposal is to shed light on the molecular interactions between coat components, and understand their role in determination of coat architecture and membrane shape. We will use a combination of structural and functional approaches to characterise COPII coat assembly, and its relationship with membranes in systems of increasing complexity, ranging from in vitro reconstitutions to cells. In particular, we will use cryo-electron tomography and subtomogram averaging to understand the architecture of the coat layers in these systems. These are fast-developing techniques that uniquely target complex structures while achieving high resolutions. With my lab at the forefront of current advances, we are perfectly placed to obtain a complete view of the COPII coat assembled on membranes. Our research will answer outstanding questions in the membrane trafficking field and open new perspectives to tackle ill-characterised regulation systems.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "CRYTOCOP" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

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

More projects from the same programme (H2020-EU.1.1.)

CARBYNE (2020)

New carbon reactivity rules for molecular editing

Read More  

CHIPTRANSFORM (2018)

On-chip optical communication with transformation optics

Read More  

CohoSing (2019)

Cohomology and Singularities

Read More