PASSMEMBRANE

Passive membrane transport of organic compounds

 Coordinatore THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE 

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 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 1˙193˙758 €
 EC contributo 1˙193˙758 €
 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-StG_20091118
 Funding Scheme ERC-SG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-12-01   -   2015-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Dr.
Nome: Ulrich Felix
Cognome: Keyser
Email: send email
Telefono: +44 1223 337272
Fax: +44 1223 337000

UK (CAMBRIDGE) hostInstitution 1˙193˙758.80
2    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Ms.
Nome: Renata
Cognome: Schaeffer
Email: send email
Telefono: +44 1223 333543
Fax: +44 1223 332988

UK (CAMBRIDGE) hostInstitution 1˙193˙758.80

Mappa


 Word cloud

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

biotechnological    passive    protein    tools    fundamental    molecules    model    living    compounds    vesicles    microfluidics    organic    optimized    single    membranes    binding    lipid    holographic    channels    detection    combination    transport    tweezers    membrane    permeation    experiments    biological    optical   

 Obiettivo del progetto (Objective)

'Passive transport through lipid membranes is ubiquitous and fundamental in living systems. The aim of this proposal is to create novel biotechnological tools to study permeation of organic compounds through lipid membranes and protein pores. In particular, I will focus on strategies employed by living organisms to optimize and regulate permeation directly through their membranes. The fundamental principles are probed by creating macroscopic model systems for biological channels and membranes. Simultaneously, new microfluidic tools will allow for a screening of biological relevant organic compounds. Biotechnological experiments investigating permeation of organic molecules into single uni-lamellar vesicles will challenge the dogma of protein controlled membranes transport. Indole, an important signaling molecule for E. coli, is an ideal candidate to demonstrate the feasibility of a novel assay based on a combination of four technologies. Microfluidics provide the controlled environment, holographic optical tweezers confine single vesicles in three dimensions to facilitate ionic current detection and simultaneous auto-fluorescence detection. This unique combination will yield a scalable technology platform to test membrane permeation. However, a deeper understanding of the molecular basis for these passive transport processes is still elusive. Theory predicts that binding potentials for molecules in a protein channel, passive transport can be optimized. Combining microfluidics with holographic optical tweezers provides the optimal means to test this quantitatively. These model experiments will prove that passive transport can be enhanced and optimized by introducing binding sites in protein channels and membranes. Furthermore, the results will guide future design of e.g. antibiotics, DNA vaccines and membrane permeating drugs and fundamentally change our understanding of passive membrane transport.'

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