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RNA-Rep SIGNED

Repeating cycles of chemically-driven RNA replication within model protocells

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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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.

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

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

Map

 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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