Measuring the phase and intensity of the light in microscopy for biological sample characterization at the nanoscale

P. Bon
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Abstract

Conventional optical imaging technique are only sensitive to the light intensity. However, many other optical parameters can be probed to enhance the quantity of information retrieved from a biological sample. I will discuss in this presentation how and why measuring the so-called phase of the light. Applications both in the scope of label-free microscopy and for 3D fluorescence super-resolution will be discussed. In particular, I will show that this quantitative imaging modality allows to identify without labeling many organelles at high frame-rate and for any duration1 in living cells. Then I will move to the application of imaging both the intensity and the phase of fluorescent single emitter and demonstrate that it leads to single molecule 3D localization and 3D super-resolution even at depth in biological tissues2
在显微镜下测量光的相位和强度,用于纳米尺度的生物样品表征
传统的光学成像技术只对光强敏感。然而,可以探测许多其他光学参数来增强从生物样品中检索到的信息量。我将在这次演讲中讨论如何以及为什么测量所谓的光的相位。将讨论在无标记显微镜和3D荧光超分辨率范围内的应用。特别是,我将展示这种定量成像方式允许在高帧率和任何持续时间下识别活细胞中的许多细胞器,而无需标记。然后,我将转向成像荧光单发射器的强度和相位的应用,并证明它导致单分子3D定位和3D超分辨率,甚至在生物组织的深度2
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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