| Literature DB >> 22429382 |
Z Schilling1, E Frank, V Magidson, J Wason, J Lončarek, K Boyer, J Wen, A Khodjakov.
Abstract
Due to photobleaching and phototoxicity induced by high-intensity excitation light, the number of fluorescence images that can be obtained in live cells is always limited. This limitation becomes particularly prominent in multidimensional recordings when multiple Z-planes are captured at every time point. Here we present a simple technique, termed predictive-focus illumination (PFI), which helps to minimize cells' exposure to light by decreasing the number of Z-planes that need to be captured in live-cell 3D time-lapse recordings. PFI utilizes computer tracking to predict positions of objects of interest (OOIs) and restricts image acquisition to small dynamic Z-regions centred on each OOI. Importantly, PFI does not require hardware modifications and it can be easily implemented on standard wide-field and spinning-disc confocal microscopes.Entities:
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Year: 2012 PMID: 22429382 PMCID: PMC3582196 DOI: 10.1111/j.1365-2818.2012.03605.x
Source DB: PubMed Journal: J Microsc ISSN: 0022-2720 Impact factor: 1.758