CSRR

Correlative Super Resolution and Real-Time Imaging of Herpes Virus Infection

 Coordinatore FUNDACIO INSTITUT DE CIENCIES FOTONIQUES 

 Organization address address: AVINGUDA CARL FRIEDRICH GAUSS 3
city: Castelldefels
postcode: 8860

contact info
Titolo: Ms.
Nome: Dolors
Cognome: Mateu
Email: send email
Telefono: 34935534053

 Nazionalità Coordinatore Spain [ES]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 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-2010-RG
 Funding Scheme MC-IRG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-03-01   -   2015-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    FUNDACIO INSTITUT DE CIENCIES FOTONIQUES

 Organization address address: AVINGUDA CARL FRIEDRICH GAUSS 3
city: Castelldefels
postcode: 8860

contact info
Titolo: Ms.
Nome: Dolors
Cognome: Mateu
Email: send email
Telefono: 34935534053

ES (Castelldefels) coordinator 100˙000.00

Mappa


 Word cloud

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

biological    time    techniques    imaging    virus    hsv    technique    mechanism    dynamic    sub    fluorescence    limitation    infection    correlative    real    cellular    resolution    super    overcome    dynamics   

 Obiettivo del progetto (Objective)

'Fluorescence imaging is a powerful technique that has transformed our understanding of biology. Recently, a number of techniques have been developed that overcome one of the fundamental limitations of fluorescence imaging, namely the diffraction limit. With these techniques, it is now possible to resolve sub-cellular architecture in multiple colors and 3D with unprecedented detail. However, the main limitation of these techniques has been the slow acquisition times making it difficult to study dynamic processes. Since biological samples are inherently highly dynamic, this limitation is a major hurdle that needs to be overcome. I will develop a correlative fluorescence imaging technique that combines the capabilities of super resolution and real-time imaging. With this correlative technique it will be possible to observe the dynamics of a biological sample in real-time and subsequently “freeze” the dynamics (by fixation or low temperature) at a time of interest to obtain a super resolution image. The dynamics can therefore be correlated with ultrastructural information, combining the capabilities of real-time and super resolution imaging. I will apply this correlative imaging technique to study infection mechanism of Herpes Simplex Virus (HSV). HSV is a medically important virus that infects neurons and epithelial cells. Besides the health hazards that it poses, HSV also has important implications in gene therapy. However, the details of HSV infection mechanism remain poorly understood. Since HSV infection involves dynamic interactions between virus particles and sub-cellular components, both of which are tens of nanometers in length scale, this is an ideal model system in which the correlative super resolution and real-time imaging technique will lead to important insights that were previously unattainable.'

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