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

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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