EVOLNA

Evolution of LNA Aptamers

 Coordinatore SYDDANSK UNIVERSITET 

Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.

 Nazionalità Coordinatore Denmark [DK]
 Totale costo 2˙497˙720 €
 EC contributo 2˙497˙720 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2010-AdG_20100317
 Funding Scheme ERC-AG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-04-01   -   2016-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    SYDDANSK UNIVERSITET

 Organization address address: CAMPUSVEJ 55
city: ODENSE M
postcode: 5230

contact info
Titolo: Mr.
Nome: Per Trolle
Cognome: Jørgensen
Email: send email
Telefono: +45 65502583
Fax: +45 65504385

DK (ODENSE M) hostInstitution 2˙497˙720.00
2    SYDDANSK UNIVERSITET

 Organization address address: CAMPUSVEJ 55
city: ODENSE M
postcode: 5230

contact info
Titolo: Prof.
Nome: Jesper Thagaard
Cognome: Wengel
Email: send email
Telefono: +45 65502510
Fax: +45 65504385

DK (ODENSE M) hostInstitution 2˙497˙720.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

lna    drug    selex    modification    biostability    aptamers    aptamer    evolution    post    size    extensive   

 Obiettivo del progetto (Objective)

'Aptamers are single-stranded oligonucleotides which are able to target peptides, proteins, small molecules or live cells by virtue of their well-defined three-dimensional shapes. Aptamers are typically generated by evolution of specific sequences against a given target by in vitro evolution using the process known as SELEX. Progress of this field with respect to drug development has so far been hampered by the relative large size and poor biostability of evolved aptamers composed of unmodified nucleotides, necessitating tedious and extensive post-SELEX truncation and modification approaches. LNA (locked nucleic acid) is a prominent nucleotide modification which is in the process of revolutionizing gene silencing and RNA detection. LNA however has never been included in de novo aptamer evolution. EVOLNA is an ambitious but coherent research program with the objective of transforming the field of aptamer technology. The vision is to enable evolution of aptamers that per se possess most of the desired properties, thereby alleviating the need for extensive post-SELEX procedures. This will be realized by combining the unique properties of LNA with innovative methods for LNA aptamer evolution. LNA aptamer technology is envisioned to enable evolution of aptamers displaying maximum chemical diversity, minimum size and high biostability. The developed strategies will be applicable not only towards evolution of therapeutic aptamers, which will be the main subject of this program, but also towards evolution of aptamers for biosensing, diagnostic and imaging applications. The program is at the very frontier of biotechnology research and spans the areas of chemistry, molecular biology and drug research.'

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