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PolControl SIGNED

Engineering translation machinery to produce light-responsive protein-polymers

Total Cost €

0

EC-Contrib. €

0

Partnership

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 PolControl project word cloud

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

inadequate    protein    biophysical    biology    libraries    overcome    elongation    precludes    function    structures    create    chemical    trna    translation    azobenzenes    interrogation    platform    biological    agents    assembly    saas    synthetase    cells    visible    marrying    biologically    substituted    direct    elucidate    components    generate    sequence    incorporation    chemistry    multiple    technologies    utilize    complexity    temporal    directing    precise    evolution    spatio    generating    machinery    engineering    manipulation    genomic    co    macromolecular    hinders    photochemical    identical    biomaterials    physical    cellular    constitute    site    materials    light    efforts    smart    polypeptide    classes    select    incorporated    formulations    self    synthesis    biomaterial    methodology    limitation    engineer    groups    extra    amino    synthetic    aminoacyl    azobenzene    acids    containing    universal    natural    versatile    demand    responsive    excludes    limits    functional    discovered    deepen    proteins    apparatus   

Project "PolControl" data sheet

The following table provides information about the project.

Coordinator
BEN-GURION UNIVERSITY OF THE NEGEV 

Organization address
address: .
city: BEER SHEVA
postcode: 84105
website: www.bgu.ac.il

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 Israel [IL]
 Total cost 1˙328˙712 €
 EC max contribution 1˙328˙712 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2017
 Duration (year-month-day) from 2017-11-01   to  2022-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    BEN-GURION UNIVERSITY OF THE NEGEV IL (BEER SHEVA) coordinator 1˙328˙712.00

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 Project objective

A general and versatile technology to engineer visible light-responsive biological agents will enable spatio-temporal manipulation and interrogation of proteins, pathways, and cells, and the design of “smart” biomaterials that can direct and respond to biological processes on-demand. Site specific incorporation of multiple visible-light-responsive chemical groups at the polypeptide level will constitute a universal methodology for precise production of light-responsive proteins and protein-based materials. However, inadequate engineering of the protein translation apparatus limits the number and complexity of chemical groups that can be incorporated into proteins as synthetic amino acids (sAAs). This limitation precludes the incorporation of recently discovered visible-light-responsive chemical groups, hinders protein engineering efforts, and excludes production of biomaterials in which multiple identical sAAs provide new physical or biophysical properties. We propose to overcome this challenge by generating a genomic-engineering based platform for co-evolution of multiple components of the translation machinery (the aminoacyl tRNA synthetase, tRNA, and elongation factor) to select for cellular machinery capable of multi-site incorporation of highly substituted azobenzenes with a range of biologically relevant photochemical properties. We will then utilize these translation systems to produce libraries of azobenzene-containing protein-based materials to elucidate the sequence-function requirements for directing light-responsive self-assembly of macromolecular structures, and to generate biomaterial formulations for control of various intra- and extra-cellular processes. By developing and marrying technologies in synthetic biology, chemistry, and biomaterials, this study will enable the synthesis of light-responsive proteins, deepen our understanding of natural and evolved translation systems, and create new classes of functional light-responsive biomaterials.

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

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