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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.

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

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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