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Orgasome SIGNED

Protein synthesis in organelles

Total Cost €

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EC-Contrib. €

0

Partnership

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 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.

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

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.

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

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