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

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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