Opendata, web and dolomites

INAME SIGNED

Imaging nucleic acid metabolism in cells

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 INAME project word cloud

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

labelling    modified    synthesis    mechanisms    interplay    chemist    diels    kumar    acid    techniques    fluorescence    acids    team    cytotoxicity    pawan    demand    harsh    deoxyuridine    life    dna    detect    deeper    ligation    slow    quantify    nucleosides    copper    labour    requirement    regulating    azide    subsequent    alkyne    earlier    free    viral    oxford    insights    label    ions    cancer    intact    biology    reaction    transcription    replication    obtain    rna    fluorophores    alternative    pioneer    antibodies    none    thymidine    reactions    nucleic    strain    brown    cells    fluorescent    prepare    effect    3h    derivative    living    university    either    incorporation    intensive    metabolism    isolate    detection    newly    seek    inverse    therapies    tom    cuaac    cycle    alder    stable    ethynyl    toxic    carry    anti    dye    catalyzed    promoted    click    cellular    bromo    professor    synthesized    proliferating    restricts    chemistry    interdisciplinary    electron    salts    cycloaddition    metal    antimetabolites   

Project "INAME" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD 

Organization address
address: WELLINGTON SQUARE UNIVERSITY OFFICES
city: OXFORD
postcode: OX1 2JD
website: www.ox.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 http://www.browngroupnucleicacidsresearch.org.uk
 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 2016
 Duration (year-month-day) from 2016-01-04   to  2018-01-03

 Partnership

Take a look of project's partnership.

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

Map

 Project objective

In this project I, Pawan Kumar, a Nucleic Acid Chemist seek to team up with a pioneer in Nucleic Acid Chemistry and Biology (Professor Tom Brown) to carry out a highly interdisciplinary study at the University of Oxford to obtain deeper insights into DNA and RNA synthesis and metabolism in living cells and its application to cancer research. I propose to detect and quantify nucleic acid synthesis in proliferating cells by fluorescence without the requirement for toxic metal ions or antibodies. Earlier known methods such as [3H]thymidine and 5-bromo-2'-deoxyuridine labelling are either slow and labour intensive or require the use of harsh conditions. Incorporation of 5-ethynyl-2'-deoxyuridine into newly synthesized DNA and its subsequent detection with an azide derivative of a fluorescent dye under copper catalyzed alkyne azide cycloaddition (CuAAC) reaction conditions presents a better alternative. However, cytotoxicity of copper salts restricts its use for living cells. I will use the strain promoted alkyne azide cycloaddition reaction, Diels-Alder reaction, and inverse electron demand Diels-Alder reaction to study cellular DNA and RNA. None of these reactions require the use of toxic metal salts. I will develop the conditions under which both DNA and RNA will be stable, so that it will be possible to isolate intact fluorescent nucleic acids from cells for detailed analysis. I will prepare the modified nucleosides and use them to label newly synthesized DNA and RNA in cells enabling their detection by reaction with fluorophores by using metal free click ligation reactions. The study will provide a better understanding of the mechanisms regulating DNA replication and the interplay between transcription and DNA replication. In the project I will develop techniques to provide information on the toxic effect of antimetabolites used commonly in anti-cancer therapies, and for identifying the mechanisms of viral replication and understanding the viral life cycle.

 Publications

year authors and title journal last update
List of publications.
2017 Pawan Kumar, Afaf H. El-Sagheer, Lynda Truong, Tom Brown
Locked nucleic acid (LNA) enhances binding affinity of triazole-linked DNA towards RNA
published pages: 8910-8913, ISSN: 1359-7345, DOI: 10.1039/C7CC05159J
Chemical Communications 53/63 2019-06-13

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "INAME" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

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

More projects from the same programme (H2020-EU.1.3.2.)

CINEMA (2019)

Creating an Infrastructure for the Numerical Exploration of Metallurgical Alloys

Read More  

GLIOHAB (2019)

Multiparametric imaging of glioblastoma tumour heterogeneity for supporting treatment decisions and accurate prognostic estimation

Read More  

UNITE (2019)

Unification Through Law: The Court of Justice of the European Union as Cultural-Moral Agent

Read More