The dissection of the molecular circuitries at the base of cell life and the identification of their abnormal transformation during carcinogenesis rely on the characterization of biological phenotypes generated by targeted overexpression or deletion of gene products through genetic manipulation. Fluorescence microscopy provides a wide variety of tools to monitor cell life with minimal perturbations. The observation of living cells requires the selection of a correct balance between temporal, spatial and "statistical" resolution according to the process to be analyzed. In the following paper ad hoc developed optical tools for dynamical tracking from cellular to molecular resolution will be presented. Particular emphasis will be devoted to discuss how to exploit light-matter interaction to selectively target specific molecular species, understanding the relationships between their intracellular compartmentalization and function.

Understanding biological dynamics : following cells and molecules to track functions and mechanisms / A. Palamidessi, I. Testa, E. Frittoli, S. Barozzi, M. Garrè, D. Mazza, P.P. Di Fiore, A. Diaspro, G. Scita, M. Faretta. - In: EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS. - ISSN 0175-7571. - 39:6(2010 May), pp. 947-957. ((Intervento presentato al 19. convegno Meeting of the Italian-Society-of-Pure-and-Applied-Biophysics tenutosi a Roma nel 2008 [10.1007/s00249-009-0461-x].

Understanding biological dynamics : following cells and molecules to track functions and mechanisms

P.P. Di Fiore;G. Scita
Penultimo
;
2010

Abstract

The dissection of the molecular circuitries at the base of cell life and the identification of their abnormal transformation during carcinogenesis rely on the characterization of biological phenotypes generated by targeted overexpression or deletion of gene products through genetic manipulation. Fluorescence microscopy provides a wide variety of tools to monitor cell life with minimal perturbations. The observation of living cells requires the selection of a correct balance between temporal, spatial and "statistical" resolution according to the process to be analyzed. In the following paper ad hoc developed optical tools for dynamical tracking from cellular to molecular resolution will be presented. Particular emphasis will be devoted to discuss how to exploit light-matter interaction to selectively target specific molecular species, understanding the relationships between their intracellular compartmentalization and function.
Cell tracking; Fluorescence microscopy; Fluorescence recovery after photobleaching; Photoactivation; Two-photon microscopy
Settore MED/04 - Patologia Generale
mag-2010
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/150908
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