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TS4NC SIGNED

TS4NC: Therapeutic S4N Chelation targeting Alzheimer's Disease.

Total Cost €

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EC-Contrib. €

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Partnership

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 TS4NC project word cloud

Explore the words cloud of the TS4NC project. It provides you a very rough idea of what is the project "TS4NC" about.

forms    consideration    ions    redox    enormous    industry    arrest    inflammatory    pharmaceutical    shed    synergistic    academia    trials    beta    physiological    active    contrary    atcun    alzheimer    neuroglia    circulation    metals    complexes    reduce    mpacs    treatment    oxidative    scientific    career    hypotheses    agents    metal    neuroprotection    releasing    neuronal    fellowship    assisting    carry    redistributing    chelating    significantly    selectivity    homeostasis    conclude    decade    natural    horizons    maturity    helping    clinical    failed    herein    biometal    put    strategy    cu    eliminating    activation    planar    last    discovery    candidate    despite    back    mcsa    greatest    drug    equally    nonregulated    attenuating    terminus    anti    simply    peptides    square    inhibit    aggregates    novelty    linked    cascade    affinity    professional    efforts    prevailing    multifunctional    aggregation    copper    4n    protein    disease    carriers    perform    cells    cycles    discovering    ad    mimics    s4n    compounds    lies    neurons    organism    class    regulation    stress    light    act    peptide    normal    motif    sequester    ts4nc    restoration    amyloid    delivering    boost    brain    s4ns   

Project "TS4NC" data sheet

The following table provides information about the project.

Coordinator
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE 

Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ
website: http://www.imperial.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]
 Total cost 212˙933 €
 EC max contribution 212˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2019
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2020
 Duration (year-month-day) from 2020-09-01   to  2022-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK (LONDON) coordinator 212˙933.00

Map

 Project objective

Despite enormous research efforts across academia and pharmaceutical industry, all clinical trials over the last decade have failed in finding a treatment for Alzheimer’s Disease (AD) which remains one of the greatest challenges in drug discovery. Taking consideration all together three prevailing AD hypotheses: Amyloid Cascade, Metal Ions and Oxidative Stress, researchers conclude that loss of neurons is due to a high level of oxidative stress produced by nonregulated redox active metal ions such as copper linked to different forms/aggregates of amyloid-β (Aβ) peptides. Therefore, the regulation of metal homeostasis is a key target for drug development. Herein, we propose a new class of multifunctional agents – S4Ns, which not only sequester Cu ions from their Aβ complexes and arrest their redox cycles, thus reduce oxidative stress in the neuronal cells, inhibit Aβ aggregation, inhibit neuroglia activation and provide anti-inflammatory effects, delivering overall neuroprotection, but also put Cu back into normal physiological circulation by releasing Cu to natural Cu-carriers. The key novelty of this approach lies in that S4N mimics the N-terminus of Aβ4-x peptide (ATCUN motif), providing 4N square planar Cu(II) coordination with high affinity and selectivity. In general, S4Ns do not act as traditional chelating agents by simply eliminating metals from the organism, on the contrary they perform as Metal–Protein Attenuating Compounds (MPACs) by redistributing and assisting in the restoration of brain biometal homeostasis. This synergistic but novel strategy will allow us to carry out a comprehensive study of the new compounds and shed light into discovering promising drug candidate. Of equally importance, TS4NC MCSA will open new research horizons and significantly boost scientific career of the applicant, by helping her to reach professional maturity during the fellowship.

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