Abstract
Light-sheet microscopy is a useful tool for performing biological investigations of thick samples and it has recently been demonstrated that it can also act as a suitable architecture for super-resolution imaging of thick biological samples by means of individual molecule localization. However, imaging in depth is still limited since it suffers from a reduction in image quality caused by scattering effects. This paper sets out to investigate the advantages of non-linear photoactivation implemented in a selective plane illumination configuration when imaging scattering samples. In particular, two-photon excitation is proven to improve imaging capabilities in terms of imaging depth and is expected to reduce light-sample interactions and sample photo-damage. Here, two-photon photoactivation is coupled to individual molecule localization methods based on light-sheet illumination (IML-SPIM), allowing super-resolution imaging of nuclear pH2AX in NB4 cells. © 2013 Cella Zanacchi et al.
Cite
CITATION STYLE
Cella Zanacchi, F., Lavagnino, Z., Faretta, M., Furia, L., & Diaspro, A. (2013). Light-Sheet Confined Super-Resolution Using Two-Photon Photoactivation. PLoS ONE, 8(7). https://doi.org/10.1371/journal.pone.0067667
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