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.

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

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.)

CREDit (2020)

Chronological REference Datasets and Sites (CREDit) towards improved accuracy and precision in luminescence-based chronologies

Read More  

DEF2DEV (2019)

Identification of the mode of action of plant defensins during root development and plant defense responses.

Read More  

NarrowbandSSL (2019)

Development of Narrow Band Blue and Red Emitting Macromolecules for Solution-Processed Solid State Lighting Devices

Read More