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ProFF SIGNED

Programming in vitro evolution using molecular fitness functions

Total Cost €

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EC-Contrib. €

0

Partnership

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 ProFF project word cloud

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

sequencing    individual    unlimited    possibly    arduous    revolution    limited    pcr    model    bottleneck    close    genetic    awesome    catalytic    programmable    versatile    programming    efficiency    scouts    knobs    laboratory    integrate    selectivity    compartmentalized    score    programmability    scoring    enzymes    computer    directed    dna    vitro    industrial    tools    chemistry    genotype    biochemical    candidate    compartments    emulsions    perspectives    lacks    programs    breakthroughs    expression    co    tunable    functions    computational    evolution    labor    experimental    droplet    few    introducing    autonomously    faster    extensively    itself    experiments    silico    remove    function    modified    enzymatic    fast    libraries    computers    hoc    intensive    combinatorial    propagate    chemistries    generation    precision    predefined    ad    green    signature    mechanisms    revamped    billions    virtuous    dynamics    quantitative    tuning    natural    micrometric    catalysts    perform    circle    assisted    molecular    fitness    phenotypic    allowed    tool    biopolymer    stages    environments    landscape   

Project "ProFF" data sheet

The following table provides information about the project.

Coordinator
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS 

Organization address
address: RUE MICHEL ANGE 3
city: PARIS
postcode: 75794
website: www.cnrs.fr

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 France [FR]
 Total cost 2˙141˙379 €
 EC max contribution 2˙141˙379 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2014-CoG
 Funding Scheme ERC-COG
 Starting year 2015
 Duration (year-month-day) from 2015-09-01   to  2020-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS FR (PARIS) coordinator 2˙141˙379.00

Map

 Project objective

Natural enzymes are awesome catalysts, in terms of their catalytic efficiency, selectivity, control mechanisms, etc. Revamped as laboratory or industrial tools, they have allowed more than a few breakthroughs, such as PCR, next generation sequencing or green chemistry. The next revolution will be brought by a new generation of extensively modified “enzymatic” catalysts working in non-natural environments, possibly build from non-natural chemistries and targeting an unlimited range of non-natural functions. However, their design is still an arduous process; computational design lacks precision while the combinatorial approach, directed evolution, is limited by labor-intensive or ad hoc selection stages.

We will remove the selection bottleneck in directed evolution by introducing biochemical computers able to perform this step autonomously. Based on recent developments in DNA-based molecular programming, these molecular scouts will be co-compartmentalized with genetic libraries into billions of individual compartments in micrometric emulsions. At each generation and in each droplet, after expression of the genotype, these molecular programs will autonomously: i- evaluate the phenotypic signature of a candidate, ii- integrate this information into a predefined scoring function and iii- propagate the relevant genetic information according to this score.

The programmability of this approach will make directed evolution versatile, faster, and able to address more challenging problems. The evolution dynamics itself become tunable, offering new perspectives on the fitness landscape of biopolymer catalysts. A quantitative in silico model will be built and integrated in a computer-assisted tool for the fast set-up of in vitro experiments and tuning of the various experimental knobs. Overall, we will close a virtuous circle by evolving the molecular tools enabling the programmable selection of the next generation of catalytic tools.

 Publications

year authors and title journal last update
List of publications.
2017 G. Gines, A. S. Zadorin, J.-C. Galas, T. Fujii, A. Estevez-Torres, Y. Rondelez
Microscopic agents programmed by DNA circuits
published pages: 351-359, ISSN: 1748-3387, DOI: 10.1038/nnano.2016.299
Nature Nanotechnology 12/4 2019-05-31
2017 Zadorin, Anton S.; Rondelez, Yannick
Natural selection in compartmentalized environment with reshuffling
published pages: , ISSN: , DOI:
1 2019-04-18
2018 Adèle Dramé-Maigné, Anton Zadorin, Iaroslava Golovkova, Yannick Rondelez
Quantifying the performance of high-throughput directed evolution protocols
published pages: , ISSN: , DOI:
2019-04-18
2017 Anton S. Zadorin, Yannick Rondelez
Selection strategies for randomly distributed replicators
published pages: , ISSN: , DOI:
2019-04-18
2016 Kevin Montagne, Guillaume Gines, Teruo Fujii, Yannick Rondelez
Boosting functionality of synthetic DNA circuits with tailored deactivation
published pages: 13474, ISSN: 2041-1723, DOI: 10.1038/ncomms13474
Nature Communications 7 2019-05-31

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

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