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FUNC NGS

Deep screening of proteins with a next generation sequencing platform

Total Cost €

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EC-Contrib. €

0

Partnership

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 FUNC NGS project word cloud

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

dr    protein    spytag    cambridge    readily    variant    units    medimmune    bioinformatics    platform    generation    solving    flow    indispensable    spycatcher    personalized    display    first    drug    intensively    secondment    altered    massively    molecular    bacterial    expertise    science    radically    deep    biology    clusters    paired    screening    oligonucleotide    complementary    hollfelder    homing    group    compatible    opening    excellent    parallel    ivc    modified    genomics    laboratory    vitro    techniques    possibilities    transformative    situ    adhesin    manner    function    tool    sequence    engineering    generalizable    university    creation    describes    links    subsequently    synergistically    medicine    showcase    cell    combined    hybridization    synthetic    monoclonal    technique    pairs    functional    limited    termed    acute    specificity    perfect    free    created    discovery    demanding    snap    func    dna    facilities    hosts    ngs    illumina    next    combines    bind    stage    sequencing    mature    modifying    sequencer    contain    sequences    therapeutic    desired   

Project "FUNC NGS" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.ac.uk

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]
 Project website https://www.bioc.cam.ac.uk/hollfelder
 Total cost 195˙454 €
 EC max contribution 195˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-08-01   to  2017-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 195˙454.00

Map

 Project objective

Next generation sequencing (NGS) has become an indispensable tool for system biology and has recently been adopted in protein engineering science as well. This proposal describes the development of a highly generalizable technique, termed FUNC-NGS, which links in situ functional information of protein activity with the function-determining DNA sequence in a massively parallel manner opening exciting possibilities, e.g., in drug discovery. In this method a cell-free display platform is combined with NGS by modifying protein display units to contain unique homing oligonucleotide sequences. These units are subsequently targeted to bind monoclonal DNA clusters in the flow cell of an Illumina sequencer by complementary DNA hybridization. FUNC-NGS is readily compatible with a paired-end sequencing programme on the Illumina platform and the number of screening units is only limited by the number of DNA clusters on the flow cell. As the first application challenge, a new variant of a modified bacterial adhesin, Spycatcher, will be created with an altered specificity for synthetic biology applications. Novel Spycatcher-SpyTag pairs are intensively desired but their creation is demanding. Solving this problem will be a perfect showcase for this radically novel deep screening technology. At the mature stage FUNC-NGS will be a transformative platform in therapeutic protein development, functional genomics and personalized medicine. The proposed work will be carried out at Dr. Hollfelder´s laboratory at the University of Cambridge with a short secondment at Medimmune. Hollfelder group has developed SNAP display, which is a FUNC-NGS-compatible in vitro protein display system. Furthermore, the University hosts excellent facilities for NGS sequencing and experienced bioinformatics support is available. The planned research programme synergistically combines my expertise in molecular biology method development with the hosts expertise in cell-free display and IVC-techniques.

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