Opendata, web and dolomites

MemDense SIGNED

Cellular control of membrane protein density in the endoplasmic reticulum via the unfolded protein response

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 MemDense project word cloud

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

organelles    genetic    valuable    density    endoplasmic    controlled    senses    centrally    parallel    triggers    metabolism    combining    exclusively    all    folding    activation    questions    infections    survival    homeostasis    cells    decisions    perspective    cellular    apoptosis    establishing    balance    synthesis    sensed    biophysical    aberrancies    viral    memdense    mount    vivo    chaperone    quality    isolation    transducers    strategies    upr    adaptive    reticulum    machinery    biology    homeostatic    soluble    stress    provides    protein    abundant    almost    tools    chronic    answer    lipid    diabetes    er    lipids    crowding    endeavor    reconstitute    neurodegeneration    abundance    sense    imbalances    radically    immuno    sensing    primed    functions    signals    misfolded    responses    molecular    recognition    conceptual    framework    vitro    membrane    diseases    proteins    characterization    mechanisms    central    cell    community    controls    biochemical    unfolded    combination   

Project "MemDense" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAT DES SAARLANDES 

Organization address
address: CAMPUS
city: SAARBRUCKEN
postcode: 66123
website: www.uni-saarland.de

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 Germany [DE]
 Total cost 1˙934˙065 €
 EC max contribution 1˙934˙065 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-COG
 Funding Scheme ERC-COG
 Starting year 2020
 Duration (year-month-day) from 2020-04-01   to  2025-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAT DES SAARLANDES DE (SAARBRUCKEN) coordinator 1˙934˙065.00

Map

 Project objective

All cells must balance the production of proteins and lipids to maintain membrane functions. Imbalances in protein folding and lipid metabolism cause endoplasmic reticulum (ER) stress associated with a wide range of complex diseases including diabetes, neurodegeneration, and viral infections. The central homeostatic program of the ER is the unfolded protein response (UPR), which senses unfolded proteins in the ER to control protein synthesis, chaperone abundance, and lipid metabolism. Through these mechanisms, the UPR centrally controls decisions between cell survival, adaptation, and apoptosis. The field has focused almost exclusively on soluble proteins as triggers of the UPR, while the more abundant membrane proteins have been neglected. Our finding of UPR activation by membrane aberrancies provides a radically new perspective and allows us to address central questions in membrane and cell biology: How is the density of ER membrane proteins sensed and controlled? How are misfolded membrane proteins recognized to mount adaptive responses?

Focusing on the conceptual advance that UPR transducers sense signals from the membrane, we will 1) establish and reconstitute the machinery for sensing membrane protein crowding, 2) identify mechanisms coordinating protein and lipid homeostasis between organelles, 3) study the molecular recognition of misfolded membrane proteins by the UPR.

Key to this endeavor is our unique combination of genetic, biochemical, and biophysical tools for parallel characterization of the UPR in vivo and in vitro. Combining this framework with novel strategies for an immuno-isolation of organelles, we are primed to answer how membrane aberrancies cause chronic ER stress. By establishing the UPR as a quality control system for membrane proteins, and providing novel tools and valuable resources to the community, MemDense will have wide impact on our molecular and cellular understanding of ER homeostasis and the many diseases related to ER stress.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "MEMDENSE" 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 "MEMDENSE" are provided by the European Opendata Portal: CORDIS opendata.

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

CHIPTRANSFORM (2018)

On-chip optical communication with transformation optics

Read More  

CohoSing (2019)

Cohomology and Singularities

Read More  

CUSTOMER (2019)

Customizable Embedded Real-Time Systems: Challenges and Key Techniques

Read More