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RNA-Rep SIGNED

Repeating cycles of chemically-driven RNA replication within model protocells

Total Cost €

0

EC-Contrib. €

0

Partnership

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 RNA-Rep project word cloud

Explore the words cloud of the RNA-Rep project. It provides you a very rough idea of what is the project "RNA-Rep" about.

multidisciplinary    yield    cooling    nucleic    strands    copying    optimise    activated    single    denatured    combines    nucleotides    synthesis    unexplored    melting    protocellular    me    biophysics    bilayer    effort    replication    leakage    emergence    cycles    solution    melted    expertise    extensive    membrane    evolution    acids    monomers    membranes    temperatures    critical    power    chemically    feeding    living    give    lipid    darwinian    absence    containing    oligo    compartments    separate    amplification    onset    simplistic    amplify    physically    science    replicated    training    rna    enzymatic    recover    transition    original    supramolecular    strand    ultimately    genetically    duplex    induce    organic    innovative    stage    fraction    outcompetes    rounds    situ    put    impermeability    renewed    biochemistry    slow    partial    structures    deciphering    kinetically    stand    heating    place    chemical    subsequent    inhibiting    biology    temperature    excellent    stochastic    unsolved    encoded    chemistry    permeable    strength    annealing    separation    prebiotic    re    repeated    template    enzymes    defects    separated   

Project "RNA-Rep" data sheet

The following table provides information about the project.

Coordinator
UNITED KINGDOM RESEARCH AND INNOVATION 

Organization address
address: POLARIS HOUSE NORTH STAR AVENUE
city: SWINDON
postcode: SN2 1FL
website: n.a.

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 United Kingdom [UK]
 Total cost 224˙933 €
 EC max contribution 224˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-04-01   to  2021-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNITED KINGDOM RESEARCH AND INNOVATION UK (SWINDON) coordinator 224˙933.00

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 Project objective

Deciphering how nucleic acids replicated in the absence of genetically encoded enzymes is of critical importance to understanding the onset of Darwinian evolution. While much effort has been put into developing chemically-driven copying of RNA exploiting activated monomers, many unsolved issues stand in the way of achieving repeated cycles of non-enzymatic RNA replication. Non-enzymatic copying of a template strand results in the formation of an RNA duplex, which must then be denatured in order for subsequent rounds of replication to take place. Although RNA strands can be separated by heating, re-annealing kinetically outcompetes slow non-enzymatic copying, thus inhibiting RNA amplification. One unexplored solution to this problem is to physically separate melted strands of RNA so that re-annealing is not possible. Since all known living systems exploit lipid membranes, we propose to investigate whether protocellular compartments can facilitate the emergence of simplistic chemical systems that amplify RNA. Specifically, high temperatures are known to induce both RNA strand separation and bilayer defects, ultimately allowing for the partial leakage of RNA. If the transition temperature of the lipid membrane is higher than the melting temperature of the RNA, then subsequent slow cooling would recover the original impermeability of the membrane and give rise to a fraction of protocellular structures containing stochastic numbers of single RNA strands. At this stage, feeding with permeable activated short (oligo)nucleotides would lead to renewed copying of RNA. This highly original and multidisciplinary project combines the strength of organic and supramolecular chemistry to optimise prebiotic compartments with the power of in situ non-enzymatic RNA biochemistry to yield a project of excellent, innovative science that will exploit my expertise in protocellular systems while providing me extensive training in organic synthesis, chemical biology and biophysics.

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The information about "RNA-REP" are provided by the European Opendata Portal: CORDIS opendata.

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