Photoactivation of pa-GFP in 3D

Optical tools for spatial confinement

I. Testa, M. Garrè, D. Parazzoli, S. Barozzi, I. Ponzanelli, D. Mazza, M. Faretta, A. Diaspro

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Photoactivatable fluorescent proteins represent an innovative tool for the direct observation of time dependent macromolecular events in living systems. The possibility of switching on a selected and confined subset of the expressed target proteins allows to follow biological processes reaching high signal to noise ratios. In particular, use of non-linear interactions to bring the molecules in the activated fluorescent form make it possible to extend the advantages of photoactivation to events that requires 3D spatial localization. In this work, we show the possibility to realize confined activated volumes in living cells, by employing photoactivatable green fluorescent protein (paGFP) in two-photon microscopy. The analysis of the kinetics of two-photon paGFP activation in dependence of the wavelength, the laser intensity and the exposure time is provided. This study allowed to assess the optimal conditions to induce photoactivation in living samples and to track the behaviour of tagged histone H2B during cellular division. Furthermore we investigate paGFP photoactivation under evanescent wave illumination. Total internal reflection set-up has been used to selectively activate subresolved distribution of proteins localized in the basal membrane surroundings. These two photoactivation methods provide a suitable tool for many biological applications, combining subresolved surface and in-depth three-dimensionally confined investigations.

Original languageEnglish
Pages (from-to)1219-1227
Number of pages9
JournalEuropean Biophysics Journal
Volume37
Issue number7
DOIs
Publication statusPublished - Sep 2008

Fingerprint

Green Fluorescent Proteins
Photons
Biological Phenomena
Proteins
Signal-To-Noise Ratio
Lighting
Histones
Microscopy
Lasers
Observation
Membranes

Keywords

  • Fluorescence
  • GFP
  • Photoactivatable proteins
  • Three-dimensional optical microscopy
  • Total internal reflection microscopy
  • Two-photon excitation microscopy

ASJC Scopus subject areas

  • Biophysics

Cite this

Testa, I., Garrè, M., Parazzoli, D., Barozzi, S., Ponzanelli, I., Mazza, D., ... Diaspro, A. (2008). Photoactivation of pa-GFP in 3D: Optical tools for spatial confinement. European Biophysics Journal, 37(7), 1219-1227. https://doi.org/10.1007/s00249-008-0317-9

Photoactivation of pa-GFP in 3D : Optical tools for spatial confinement. / Testa, I.; Garrè, M.; Parazzoli, D.; Barozzi, S.; Ponzanelli, I.; Mazza, D.; Faretta, M.; Diaspro, A.

In: European Biophysics Journal, Vol. 37, No. 7, 09.2008, p. 1219-1227.

Research output: Contribution to journalArticle

Testa, I, Garrè, M, Parazzoli, D, Barozzi, S, Ponzanelli, I, Mazza, D, Faretta, M & Diaspro, A 2008, 'Photoactivation of pa-GFP in 3D: Optical tools for spatial confinement', European Biophysics Journal, vol. 37, no. 7, pp. 1219-1227. https://doi.org/10.1007/s00249-008-0317-9
Testa I, Garrè M, Parazzoli D, Barozzi S, Ponzanelli I, Mazza D et al. Photoactivation of pa-GFP in 3D: Optical tools for spatial confinement. European Biophysics Journal. 2008 Sep;37(7):1219-1227. https://doi.org/10.1007/s00249-008-0317-9
Testa, I. ; Garrè, M. ; Parazzoli, D. ; Barozzi, S. ; Ponzanelli, I. ; Mazza, D. ; Faretta, M. ; Diaspro, A. / Photoactivation of pa-GFP in 3D : Optical tools for spatial confinement. In: European Biophysics Journal. 2008 ; Vol. 37, No. 7. pp. 1219-1227.
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