DODECIN

Construction of a Molecular Crane Based on the Flavoprotein Dodecin

 Coordinatore UNIVERSITAET SIEGEN 

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

 Nazionalità Coordinatore Non specificata
 Totale costo 1˙100˙000 €
 EC contributo 1˙100˙000 €
 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-2009-StG
 Funding Scheme ERC-SG
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-11-01   -   2015-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITAET SIEGEN

 Organization address address: HERRENGARTEN 3
city: SIEGEN
postcode: 57072

contact info
Titolo: Dr.
Nome: Gilbert
Cognome: Nöll
Email: send email
Telefono: +49 271 7404360
Fax: +49 271 7403270

DE (SIEGEN) hostInstitution 1˙100˙000.00
2    UNIVERSITAET SIEGEN

 Organization address address: HERRENGARTEN 3
city: SIEGEN
postcode: 57072

contact info
Titolo: Ms.
Nome: Theresa
Cognome: Stoye
Email: send email
Telefono: +49 271 740 4871
Fax: +49 271 740 14871

DE (SIEGEN) hostInstitution 1˙100˙000.00

Mappa


 Word cloud

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

crane    molecules    wire    tip    flavin    single    force    atomic    release    electrochemically    surfaces    dodecin    flavins    construction    surface    switchable    apododecin    transport    molecular   

 Obiettivo del progetto (Objective)

'The flavoprotein dodecin from the halophilic organism Halobacterium salinarum binds not only native but also artificial flavins with high affinities in their oxidized state. Reduction of the flavins induces the dissociation of the holocomplex into apododecin and free flavin. Based on these unique binding characteristics, a molecular crane shall be developed that is able to pick up and to release molecular objects through a switch of the electric potential. For this purpose, a single flavin has to be linked to the conductive tip of an atomic force microscope via a molecular wire-like subunit (flavin molecular wire AFM tip/electrode). On the basis of such an electrochemically switchable molecular crane, it will be possible to bind and release single molecules of dodecin apoprotein or even larger molecular assemblies attached to apododecin serving as molecular junction. While the construction of a molecular crane for the transport of single molecules is the main goal, the successful realization of this project fundamentally depends on the synthesis and characterization of molecular wire-like subunits, which can be used to attach redox-active proteins to surfaces in an electrochemically switchable state. Thus, functionalized single-walled carbon nanotubes or organic p-electron systems will be examined with respect to their ability to serve as molecular wire. Surface modification protocols have to be developed and modified surfaces will be investigated by a combination of atomic force microscopy, surface plasmon resonance spectroscopy, and electrochemical methods. The results of these studies will be of general interest for the construction of molecular switches, devices, and transport systems, and for the development of amperometric biosensors and biofuel cells.'

Altri progetti dello stesso programma (FP7-IDEAS-ERC)

DSBREPAIR (2008)

Developmental and Genetic Analysis of DNA Double-Strand Break Repair

Read More  

HYRAX (2010)

"Rock Hyrax Middens and Climate Change in Southern Africa during the last 50,000 years"

Read More  

PHARMASECURITY (2013)

Pharmaceuticals and Security: The Role of Public-Private Collaborations in Strengthening Global Health Security

Read More