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.

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

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.)

RAMBEA (2019)

Realistic Assessment of Historical Masonry Bridges under Extreme Environmental Actions

Read More  

PROSPER (2019)

Politics of Rulemaking, Orchestration of Standards, and Private Economic Regulations

Read More  

IRF4 Degradation (2019)

Using a novel protein degradation approach to uncover IRF4-regulated genes in plasma cells

Read More