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.

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

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.)

CohoSing (2019)

Cohomology and Singularities

Read More  

CARBYNE (2020)

New carbon reactivity rules for molecular editing

Read More  

CHIPTRANSFORM (2018)

On-chip optical communication with transformation optics

Read More