Opendata, web and dolomites

DynaGrow SIGNED

Dynamic Growth and Replication in Coacervate Protocells

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 DynaGrow project word cloud

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

appreciable    right    protocells    modifications    liquid    replicate    proteins    coacervate    membrane    dilution    act    conjugation    functionalized    reactions    modern    biggest    oligopeptides    spontaneous    sequence    sufficiently    dual    destined    instability    lack    coacervation    sequences    degree    peptides    mark    ostwald    found    building    shape    chemical    fragments    darwinian    reached    blocks    concentrates    peptide    complementary    life    fundamental    surrounding    undergo    divide    coacervates    place    compartment    exactly    chains    free    intrinsically    environment    condensed    see    division    disordered    previously    mixtures    science    active    cells    divides    mysteries    minimal    extinct    living    spontaneously    longer    complexity    inside    patterns    molecular    emergence    fuel    replication    ripening    droplets    inspired    template    templates    replicators    rates    rate    predicted    directed    either    never    molecules    evolution    stable    holds    elongation    organelles    class   

Project "DynaGrow" data sheet

The following table provides information about the project.

Coordinator
STICHTING KATHOLIEKE UNIVERSITEIT 

Organization address
address: GEERT GROOTEPLEIN NOORD 9
city: NIJMEGEN
postcode: 6525 EZ
website: www.radboudumc.nl

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 Netherlands [NL]
 Total cost 1˙500˙000 €
 EC max contribution 1˙500˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-STG
 Funding Scheme ERC-STG
 Starting year 2020
 Duration (year-month-day) from 2020-03-01   to  2025-02-28

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    STICHTING KATHOLIEKE UNIVERSITEIT NL (NIJMEGEN) coordinator 1˙500˙000.00

Map

 Project objective

Replication and division are two of the most fundamental properties of living systems. Without replication, Darwinian evolution would not be possible, and life could never have reached the degree of complexity we see today. However, exactly how mixtures of non-living molecules developed the ability to replicate and divide, remains one of the biggest mysteries in modern science. Various molecular replicators have been investigated previously, but they are all destined to become extinct by dilution, since they lack a surrounding compartment that divides spontaneously during replication.

In this proposal, we aim at developing a new class of coacervate-based protocells that are capable of active growth and template-directed replication. The coacervates we propose here are condensed liquid droplets with a unique dual role: they act as a compartment that holds together and concentrates the template molecules and the building blocks, and they provide the right chemical environment for the replication reactions to take place at an appreciable rate. The coacervate-based protocells are composed of oligopeptides with low complexity sequences, inspired by the intrinsically disordered proteins found in membrane-free organelles inside cells. Active growth is achieved through fuel-driven reactions, either by elongation of existing peptides or by specific chemical modifications at the peptide side chains that enhance their coacervation potential. Longer peptides can also act as templates for conjugation of end-functionalized peptide fragments with sequence patterns complementary to the template. Protocells with sufficiently high growth or replication rates are not only stable against Ostwald ripening, but are also predicted to undergo spontaneous division through a shape instability. This would mark a key step in the emergence of minimal cells and open the way for the evolution of more complex life-like systems.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "DYNAGROW" 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 "DYNAGROW" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

KineTic (2020)

New Reagents for Quantifying the Routing and Kinetics of T-cell Activation

Read More  

INSPIRE (2019)

System-wide discovery and analysis of inositol pyrophosphate signaling networks in plants

Read More  

CARBYNE (2020)

New carbon reactivity rules for molecular editing

Read More