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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.

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

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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