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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.

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

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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