Fast live simultaneous multiwavelength four-dimensional optical microscopy

Abstract : Live fluorescence microscopy has the unique capability to probe dynamic processes, linking molecular components and their localization with function. A key goal of microscopy is to increase spatial and temporal resolution while simultaneously permitting identification of multiple specific components. We demonstrate a new microscope platform, OMX, that enables subsecond, multicolor four-dimensional data acquisition and also provides access to subdiffraction structured illumination imaging. Using this platform to image chromosome movement during a complete yeast cell cycle at one 3D image stack per second reveals an unexpected degree of photosensitivity of fluorophore-containing cells. To avoid perturbation of cell division, excitation levels had to be attenuated between 100 and 10,000× below the level normally used for imaging. We show that an image denoising algorithm that exploits redundancy in the image sequence over space and time allows recovery of biological information from the low light level noisy images while maintaining full cell viability with no fading.
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Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2010, 107 (37), pp.16016-16022. 〈10.1073/pnas.1004037107〉
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Soumis le : lundi 29 novembre 2010 - 15:39:24
Dernière modification le : mercredi 11 avril 2018 - 01:53:21

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Peter M. Carlton, Jérôme Boulanger, Charles Kervrann, Jean-Baptiste Sibarita, Jean Salamero, et al.. Fast live simultaneous multiwavelength four-dimensional optical microscopy. Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2010, 107 (37), pp.16016-16022. 〈10.1073/pnas.1004037107〉. 〈inria-00540978〉

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