FRIVIC

FLUORESCENT ROTORS FOR IMAGING VISCOSITY IN CELLS

 Coordinatore IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE 

 Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ

contact info
Titolo: Ms.
Nome: Brooke
Cognome: Alasya
Email: send email
Telefono: +44 207 594 1181
Fax: +44 207 594 1418

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 200˙371 €
 EC contributo 200˙371 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2011-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-09-03   -   2014-09-02

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE

 Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ

contact info
Titolo: Ms.
Nome: Brooke
Cognome: Alasya
Email: send email
Telefono: +44 207 594 1181
Fax: +44 207 594 1418

UK (LONDON) coordinator 200˙371.80

Mappa


 Word cloud

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

rotors    microviscosity    therapy    imaging    domains    unavailable    applicant    cellular    environment    absorption    detection    molecular    fluorescence    biological    cells    viscosity    lifetime   

 Obiettivo del progetto (Objective)

'This project proposes to design and synthesise a series of novel fluorescent molecular rotors able to measure microviscosity of cellular domains based on the fluorescence lifetime. The fluorescence detection is an efficient and direct way to localise the molecules within cells whereas the measurement of the fluorescence lifetime provides a number of additional assets since the fluorescence decay is typically sensitive to the environment of the fluorophore. In molecular rotors the lifetime can be correlated with viscosity of their immediate environment. Besides, fluorescence lifetime is concentration independent and allows to account for the aggregation phenomenon, and other detrimental quenching processes, the data which is unavailable from the simple intensity measurements. As such, lifetime based detection of molecular rotor fluorescence will provide a quick and accurate measure of the microviscosity in individual cell domains, unavailable from other methods. The new molecular rotors, with incorporated substituents to achieve extensive electronic conjugation, will have advantageous spectroscopic properties, such as high two-photon absorption cross sections and red-shifted absorption and emission wavelengths in the tissue therapeutic window, important both for diagnostic and therapy. These new superior dyes will be used for viscosity imaging in cells, with the emphasis on measuring the viscosity of hydrophobic membranes and on the monitoring of the viscosity changes during Photodynamic Therapy (PDT), a light activated cancer treatment of clinical importance. This project has the ideal overlap of experience and expertise between the applicant and the host group. The results will be both of fundamental importance and practical significance, e.g. for the development of future imaging strategies in biological research. This fellowship will enable the applicant to learn new biology-related skills and as such will prove instrumental for her future academic career.'

Introduzione (Teaser)

Viscosity is a highly important parameter in biological systems and profoundly impacts cellular function. EU researchers have designed new systems to monitor viscosity based on molecular rotors.

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