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SYNBIO.ECM SIGNED

SYNBIO.ECM: Designer extracellular matrices to program healthy and diseased cardiac morphogenesis

Total Cost €

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EC-Contrib. €

0

Partnership

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 SYNBIO.ECM project word cloud

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

letter    clinical    extracellular    move    manufacturing    successful    synthetic    tissues    effect    model    engineers    modest    traction    tissue    microscopy    maturation    cad    parts    inputs    genetic    recapitulate    phases    programmable    fluorescence    successes    biology    trabeculation    unreliable    biotechnology    hoc    equations    compaction    synbio    transformed    models    ecm    subcellular    computational    human    cell    emerged    sequencing    solution    meet    process    experimental    tremendous    worldwide    aided    2005    medical    progressively    progress    designer    nature    heart    found    differential    situ    quantitative    predictable    stem    ordinary    cardiac    ignored    biological    super    despite    multiscale    expensive    ad    cells    dr    class    resolution    framework    individual    force    leverage    behavior    interactions    pluripotent    assemblies    endy    computationally    functions    platform    computer    largely    tools    libraries    bioprint    matrix    dna    engineering    asked   

Project "SYNBIO.ECM" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITA DEGLI STUDI DI PAVIA 

Organization address
address: STRADA NUOVA 65
city: PAVIA
postcode: 27100
website: www.unipv.it

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 Italy [IT]
 Total cost 1˙999˙375 €
 EC max contribution 1˙999˙375 € (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 2020-07-01   to  2025-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITA DEGLI STUDI DI PAVIA IT (PAVIA) coordinator 1˙999˙375.00

Map

 Project objective

To meet medical needs worldwide, tissue engineering must move from successful pre/clinical products towards an effective process to meet Worldwide medical needs, but this is challenging since a quantitative design framework has not emerged, yet. Synthetic biology (SYNBIO) was the solution that genetic engineers found to the same problem: “Despite tremendous individual successes in genetic engineering and biotechnology […], why is the engineering of useful synthetic biological systems still an expensive, unreliable and ad hoc research process?” asked Dr. Endy in a 2005 letter to Nature. The SYNBIO solution included: i) libraries of DNA parts with well-characterized effect on cells; ii) tools to computationally design system-level assemblies, or designer-DNA; and, iii) bottom-up engineering of cell functions using progressively more complex designer-DNA. Effectively, SYNBIO introduced a computer-aided design and manufacturing (CAD/M) platform that transformed the process of engineering cells. However, since inputs from the extracellular matrix (ECM) have largely been ignored, progress towards programmable tissue-level behavior have been more modest.

Here, we will build on my experience with computational and experimental models in cardiac tissue engineering to develop a CAD/M framework for engineering cardiac tissues with computationally predictable properties, or designer-ECM. To characterize ECM-cell interactions, we will use traction force and super-resolution microscopy with fluorescence in-situ sequencing. To model multiscale ECM-cell interactions, we will use ordinary differential equations and subcellular element models. Finally, we will leverage ECM parts and human induced pluripotent stem cells to bioprint designer-ECM that recapitulate three phases of heart development: trabeculation, compaction, and maturation.

With synthetic matrix biology (SYNBIO.ECM), we will develop a CAD/M-based process and a new class of products for cardiac tissue engineering.

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The information about "SYNBIO.ECM" are provided by the European Opendata Portal: CORDIS opendata.

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