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MemDense SIGNED

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

Total Cost €

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EC-Contrib. €

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Partnership

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 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.

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

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.
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 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.

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

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