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AutophagosomeSealing SIGNED

Ymr1 role in the Atg proteins release from complete autophagosomes

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 AutophagosomeSealing project word cloud

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

phosphatase    combination    regulation    molecular    cardiovascular    phagophore    survival    despite    site    edge    diseases    sequestered    model    dephosphorylating    benefit    plays    laboratory    autophagosomes    aggregates    illnesses    degradation    destruction    diversity    autoimmune    stress    chronic    maturity    phosphate    vesicles    assembly    yeast    microscopy    biology    health    invading    pathophysiology    phosphatidylinositol    pathogens    autophagy    intracellular    neurodegenerative    found    ymr1    experimental    cutting    structures    largely    specialized    therapies    atg    elucidate    independence    conceptual    proteins    membrane    mechanism    cell    host    organelles    biochemistry    advantages    location    compounds    malignancies    reinforce    muscular    concerted    regulates    double    inflammatory    fluorescence    starting    pas    professional    regulate    perspective    human    formed    techniques    action    realization    multiple    bases    protein    electron    unknown   

Project "AutophagosomeSealing" data sheet

The following table provides information about the project.

Coordinator
ACADEMISCH ZIEKENHUIS GRONINGEN 

Organization address
address: HANZEPLEIN 1
city: GRONINGEN
postcode: 9713 GZ
website: www.umcg.nl

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 Netherlands [NL]
 Project website http://cellbiology.umcg.nl/groups/reggiorigroup/
 Total cost 177˙598 €
 EC max contribution 177˙598 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-10-01   to  2017-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ACADEMISCH ZIEKENHUIS GRONINGEN NL (GRONINGEN) coordinator 177˙598.00

Map

 Project objective

Autophagy is one of the major intracellular degradation processes and it is essential for cell survival in multiple stress conditions. As a result, this pathway plays a key role in the pathophysiology of numerous illnesses including neurodegenerative, cardiovascular, chronic inflammatory, muscular and autoimmune diseases, and some malignancies. Structures targeted to destruction such as protein aggregates, organelles and invading pathogens are sequestered into double-membrane vesicles called autophagosomes. Autophagosomes are formed through the concerted action of the autophagy-related (Atg) proteins at a site specialized location known as the phagophore assembly site (PAS). Despite this knowledge, the mechanism and regulation of autophagy remain largely unknown. The host laboratory has found that Ymr1, a phosphatase dephosphorylating phosphatidylinositol-3-phosphate, plays a key role in the regulation of autophagy. The main objective of this project is to elucidate the mechanism through which Ymr1 regulates autophagy. To achieve this goal, the applicant will exploit the experimental advantages of the yeast model and use in combination cutting-edge techniques in molecular biology, biochemistry, fluorescence microscopy and electron microscopy. The results will advance our knowledge on autophagy and in a long-term perspective they will provide the conceptual bases for the development of therapies or compounds aimed to regulate autophagy to the benefit of human health. Through the realization of the project, the applicant will strongly reinforce his professional maturity, diversity and independence, essential for starting his own research activity.

 Publications

year authors and title journal last update
List of publications.
2017 Susana Abreu, Franziska Kriegenburg, Rubén Gómez‐Sánchez, Muriel Mari, Jana Sánchez‐Wandelmer, Mads Skytte Rasmussen, Rodrigo Soares Guimarães, Bettina Zens, Martina Schuschnig, Ralph Hardenberg, Matthias Peter, Terje Johansen, Claudine Kraft, Sascha Martens, Fulvio Reggiori
Conserved Atg8 recognition sites mediate Atg4 association with autophagosomal membranes and Atg8 deconjugation
published pages: 765-780, ISSN: 1469-221X, DOI: 10.15252/embr.201643146
EMBO reports 18/5 2019-06-13
2017 Jana Sánchez-Wandelmer, Franziska Kriegenburg, Sabrina Rohringer, Martina Schuschnig, Rubén Gómez-Sánchez, Bettina Zens, Susana Abreu, Ralph Hardenberg, David Hollenstein, Jieqiong Gao, Christian Ungermann, Sascha Martens, Claudine Kraft, Fulvio Reggiori
Atg4 proteolytic activity can be inhibited by Atg1 phosphorylation
published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-017-00302-3
Nature Communications 8/1 2019-06-13

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