Opendata, web and dolomites

SynBioBrain SIGNED

Building biological computers from bacterial populations

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 SynBioBrain project word cloud

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

temporal    samples    read    create    indicate    architecture    combined    biology    global    device    dollars    output    bioprocess    microbiota    industry    health    cell    chain    fatty    compounds    counting    potentially    automata    cellular    monitoring    environments    biosensors    proof    detection    hydrogel    synthetic    multiple    intestinal    processed    unnecessary    billions    formed    agents    inflammatory    molecules    sensors    detecting    distinguish    alternative    ph    disease    operations    patterning    distinguishes    strain    powerful    communicate    sophisticated    channel    distributed    logic    biomarkers    harmful    digital    populations    treatments    biosensor    perform    sensing    diagnostic    irritable    medically    single    chemical    acids    environmental    computation    biocomputers    biological    memory    stool    bacteria    transduction    bowel    computers    living    structures    move    home    quorum    construct    engineered    inflammation    save    fashion    dimensional    bacterial    physio    engineer    detector    microfluidic    care    inputs    individual    spatial    housed    biocomputer    regular    whilst    syndrome    detect    replaced    arrangements   

Project "SynBioBrain" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY COLLEGE LONDON 

Organization address
address: GOWER STREET
city: LONDON
postcode: WC1E 6BT
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 1˙998˙025 €
 EC max contribution 1˙998˙025 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-COG
 Funding Scheme ERC-COG
 Starting year 2018
 Duration (year-month-day) from 2018-05-01   to  2023-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE LONDON UK (LONDON) coordinator 1˙998˙025.00

Map

 Project objective

Biosensors detect compounds using a biological component combined with a physio-chemical detector. Using synthetic biology, we can now engineer bacteria into whole-cell biosensors where sensing, transduction and output occur within the living cell. Applications include the detection of harmful environmental agents, bioprocess monitoring, and detecting medically relevant biomarkers. As we move towards more sophisticated applications, single channel read-out will be replaced with sensors that have multiple inputs and more complex information processing capabilities. Whilst digital logic within a single strain of bacteria can be implemented, consortia offer a powerful alternative, where information is integrated and processed in a distributed fashion. This proposal sets out a research project that will construct biological computers formed from engineered bacterial populations that communicate using quorum sensing molecules. Information from multiple biosensor inputs will be integrated and processed by the biocomputer, the output of which will be spatial patterning. The architecture will be based on cellular automata, which can perform any computation, including logic and temporal logic operations, memory and counting, all of which can be used to distinguish states in complex biological and chemical environments. Our biocomputers will be housed in microfluidic devices using hydrogel structures to create two and three dimensional regular arrangements. As a proof-of-concept, we will develop a biocomputer for the analysis and monitoring of intestinal and microbiota health through stool samples. Sensors for inflammation, pH and short chain fatty acids will be combined into a device that can indicate whether an individual has inflammatory bowel disease or irritable bowel syndrome. A low-cost device for use at home, which distinguishes between these conditions, could potentially save the global health care industry billions of dollars in unnecessary diagnostic treatments.

 Publications

year authors and title journal last update
List of publications.
2019 Alex J.H. Fedorec, Tanel Ozdemir, Anjali Doshi, Yan-Kay Ho, Luca Rosa, Jack Rutter, Oscar Velazquez, Vitor B. Pinheiro, Tal Danino, Chris P. Barnes
Two New Plasmid Post-segregational Killing Mechanisms for the Implementation of Synthetic Gene Networks in Escherichia coli
published pages: 323-334, ISSN: 2589-0042, DOI: 10.1016/j.isci.2019.03.019
iScience 14 2019-11-08
2018 Philipp Boeing, Miriam Leon, Darren Nesbeth, Anthony Finkelstein, Chris Barnes
Towards an Aspect-Oriented Design and Modelling Framework for Synthetic Biology
published pages: 167, ISSN: 2227-9717, DOI: 10.3390/pr6090167
Processes 6/9 2019-11-08

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

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

AST (2019)

Automatic System Testing

Read More  

QUAMAP (2019)

Quasiconformal Methods in Analysis and Applications

Read More  

CHIPTRANSFORM (2018)

On-chip optical communication with transformation optics

Read More