Opendata, web and dolomites

Orgasome SIGNED

Protein synthesis in organelles

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 Orgasome project word cloud

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

specialized    pigments    chlororibosomal    machineries    components    molecular    produces    evolution    ribosomes    functional    head    glimpses    synthesis    coupled    tomography    gtpase    insights    chloroplasts    action    membrane    translation    mito    context    regulatory    parallel    reveal    regarding    pausing    synthesizing    ribosomal    chlororibosomes    understand    converts    central    dynamic    analyze    incorporated    incorporation    reconstitute    rrna    organelle    cytosol    particle    exclusively    systematically    energy    first    intrinsic    divaricate    questions    chemical    trans    exit    almost    organelles    spatiotemporally    fundamental    structural    mitoribosomes    assembly    contemplation    put    imported    co    stall    evolve    process    functionally    bioenergetics    organic    exhibit    showed    elucidate    maturated    tunnels    hydrophobic    oxygen    mutants    combine    subunit    counterpart    species    small    protuberance    organellar    core    complexity    single    stages    mitochondria    mechanisms    sunlight    compartments    val    pull    ultimately    samples    antibiotics    trna    responsible    whereas    translational    dynamics    proteins    operations    protein    assembled   

Project "Orgasome" data sheet

The following table provides information about the project.

Coordinator
STOCKHOLMS UNIVERSITET 

Organization address
address: UNIVERSITETSVAGEN 10
city: STOCKHOLM
postcode: 10691
website: www.su.se

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 Sweden [SE]
 Total cost 1˙331˙300 €
 EC max contribution 1˙331˙300 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 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    STOCKHOLMS UNIVERSITET SE (STOCKHOLM) coordinator 1˙331˙300.00

Map

 Project objective

Protein synthesis in mitochondria is essential for the bioenergetics, whereas its counterpart in chloroplasts is responsible for the synthesis of the core proteins that ultimately converts sunlight into the chemical energy that produces oxygen and organic matter. Recent insights into the mito- and chlororibosomes have provided the first glimpses into the distinct and specialized machineries that involved in synthesizing almost exclusively hydrophobic membrane proteins. Our findings showed: 1) mitoribosomes have different exit tunnels, intrinsic GTPase in the head of the small subunit, tRNA-Val incorporated into the central protuberance; 2) chlororibosomes have divaricate tunnels; 3) ribosomes from both organelles exhibit parallel evolution. This allows contemplation of questions regarding the next level of complexity: How these ribosomes work and evolve? How the ribosomal components imported from cytosol are assembled with the organellar rRNA into a functional unit being maturated in different compartments in organelles? Which trans-factors are involved in this process? How the chlororibosomal activity is spatiotemporally coupled to the synthesis and incorporation of functionally essential pigments? What are the specific regulatory mechanisms? To address these questions, there is a need to first to characterize the process of translation in organelles on the structural level. To reveal molecular mechanisms of action, we will use antibiotics and mutants for pausing in different stages. To reconstitute the assembly, we will systematically pull-down pre-ribosomes and combine single particle with tomography to put the dynamic process in the context of the whole organelle. To understand co-translational operations, we will stall ribosomes and characterize their partner factors. To elucidate the evolution, we will analyze samples from different species. Taken together, this will provide fundamental insights into the structural and functional dynamics of organelles.

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

SHExtreme (2020)

Estimating contribution of sub-hourly sea level oscillations to overall sea level extremes in changing climate

Read More  

CURVE-X (2019)

Industrialisation of curved sensors and related imagers

Read More