Opendata, web and dolomites

LEVERAGE mRNA SIGNED

Laboratory Evolution of Virus-likE pRotein cAGes for Eukaryotic mRNA delivery

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 LEVERAGE mRNA project word cloud

Explore the words cloud of the LEVERAGE mRNA project. It provides you a very rough idea of what is the project "LEVERAGE mRNA" about.

treating    rational    forms    mrna    microscopy    encode    mrnas    technologies    inside    recognition    container    nanocompartments    replacement    successfully    aquifex    successful    variants    thoroughly    symmetrical    capsid    delivers    enzyme    cryo    population    health    aeolicus    cell    rna    hollow    pressure    degrade    edge    leverage    designed    human    evolution    cutting    permeant    create    enclosed    proteinaceous    dysfunctional    viruses    molecules    induce    time    directed    engineer    protein    messenger    mammalian    selectively    engineering    releasing    containers    sequencing    lumazine    genes    aals    organism    starting    packaging    tag    acids    safely    initial    cytosol    action    obtain    modeling    tolerant    stimulating    disassemble    nucleic    made    lacking    encapsulates    computational    embodies    inhibiting    thereby    capsids    electron    ultimate    proteins    candidates    bacteria    therapy    eukaryotic    lasting    rnas    optimize    gene    hijacked    transport    replacing    bacterial    positive    generation    enter    synthase    oligonucleotides    performing    artificial    missing    reaching    impacts    cells    therapies    small    genetic    ribonucleic    disease   

Project "LEVERAGE mRNA" data sheet

The following table provides information about the project.

Coordinator
EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH 

Organization address
address: Raemistrasse 101
city: ZUERICH
postcode: 8092
website: https://www.ethz.ch/de.html

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 Switzerland [CH]
 Total cost 191˙149 €
 EC max contribution 191˙149 € (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 2019-05-01   to  2021-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH CH (ZUERICH) coordinator 191˙149.00

Map

 Project objective

Nucleic acids are promising candidates for treating disease by stimulating, inhibiting, or replacing other nucleic acids or proteins inside of eukaryotic cells—a process known as “gene therapy.” However, methods to efficiently and safely deliver genes into cells are still lacking. The problem is that nucleic acids are not cell permeant and degrade before reaching the cytosol. One way to transport oligonucleotides into cells is by packaging them into hollow containers made of proteins, a method that has been successfully hijacked by viruses for a long time.

Here, we propose to design and engineer an artificial proteinaceous container that (1) selectively encapsulates ribonucleic acids (RNAs) using a known RNA recognition tag and (2) delivers this RNA into the cytosol of mammalian cells. Protein engineering, which embodies both rational design and computational modeling, will be used to create the starting design of this artificial protein container. The initial design will be based on the protein lumazine synthase from the bacterial organism Aquifex aeolicus (AaLS), which forms small but highly symmetrical nanocompartments in bacteria and is very tolerant to genetic changes. To optimize this design, we will use directed evolution to induce an artificial selection pressure on a large population of distinct capsid variants, allowing us to obtain only the best-performing capsid variants: those that can enter and disassemble selectively inside of mammalian cells, thereby releasing the enclosed RNA molecules into the cytosol. New AaLS containers will be thoroughly characterized using cutting-edge technologies, such next-generation sequencing and cryo-electron microscopy.

The ultimate goal of LEVERAGE mRNA is to use the designed and evolved capsids to deliver messenger RNAs (mRNAs) into cells that encode missing or dysfunctional proteins, for example in enzyme replacement therapies. If successful, this action will have lasting positive impacts on human health.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "LEVERAGE MRNA" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "LEVERAGE MRNA" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

NSTree (2020)

Understanding substrate delivery for cell wall biosynthesis in plants

Read More  

BB-SLM (2020)

Polychromatic digital optics for structured light

Read More  

MetEpiC (2020)

P53-dependent Metabolic and Epigenetic Reprogramming in Carcinogenesis

Read More