{"title":"Measuring the phase and intensity of the light in microscopy for biological sample characterization at the nanoscale","authors":"P. Bon","doi":"10.1364/DH.2019.TH1A.1","DOIUrl":null,"url":null,"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","PeriodicalId":448778,"journal":{"name":"Digital Holography and Three-Dimensional Imaging 2019","volume":"16 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Digital Holography and Three-Dimensional Imaging 2019","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1364/DH.2019.TH1A.1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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