Motion artefact detection in structured illumination microscopy for live cell imaging

被引:19
|
作者
Foerster, Ronny [1 ,2 ]
Wicker, Kai [3 ]
Mueller, Walter [1 ,2 ]
Jost, Aurelie [1 ,2 ]
Heintzmann, Rainer [1 ,2 ]
机构
[1] Leibniz Inst Photon Technol, Albert Einstein Str 9, D-07745 Jena, Germany
[2] Friedrich Schiller Univ, Abbe Ctr Photon, Inst Phys Chem, Helmholtzweg 4, D-07743 Jena, Germany
[3] Carl Zeiss, Corp Res & Technol, Carl Zeiss Promenade 10, D-07745 Jena, Germany
来源
OPTICS EXPRESS | 2016年 / 24卷 / 19期
关键词
RESOLUTION;
D O I
10.1364/OE.24.022121
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The reconstruction process of structured illumination microscopy (*SIM) creates substantial artefacts if the specimen has moved during the acquisition. This reduces the applicability of SIM for live cell imaging, because these artefacts cannot always be recognized as such in the final image. A movement is not necessarily visible in the raw data, due to the varying excitation patterns and the photon noise. We present a method to detect motion by extracting and comparing two independent 3D wide-field images out of the standard SIM raw data without needing additional images. Their difference reveals moving objects overlaid with noise, which are distinguished by a probability theory-based analysis. Our algorithm tags motion-artefacts in the final high-resolution image for the first time, preventing the end-user from misinterpreting the data. We show and explain different types of artefacts and demonstrate our algorithm on a living cell.
引用
收藏
页码:22121 / 22134
页数:14
相关论文
共 50 条
  • [1] Structured Illumination for Live Cell Microscopy
    Richter, Verena
    Piper, Mathis
    Wagner, Michael
    Schneckenburger, Herbert
    BIOPHOTONICS: PHOTONIC SOLUTIONS FOR BETTER HEALTH CARE VI, 2018, 10685
  • [2] Live-cell imaging of human spermatozoa using structured illumination microscopy
    Opstad, Ida S.
    Popova, Daria A.
    Acharya, Ganesh
    Basnet, Purusotam
    Ahluwalia, Balpreet S.
    BIOMEDICAL OPTICS EXPRESS, 2018, 9 (12): : 5939 - 5945
  • [3] Assessing resolution in live cell structured illumination microscopy
    Pospisil, Jakub
    Fliegel, Karel
    Klima, Milos
    PHOTONICS, DEVICES, AND SYSTEMS VII, 2017, 10603
  • [4] Evaluating resolution in live cell structured illumination microscopy
    Pospisil, Jakub
    Fliegel, Karel
    Svihlik, Jan
    Klima, Milos
    APPLICATIONS OF DIGITAL IMAGE PROCESSING XLII, 2019, 11137
  • [5] Single-frame structured illumination microscopy for fast live-cell imaging
    Wu, Hanmeng
    Li, Yueming
    Sun, Yile
    Yin, Lu
    Sun, Weiyun
    Ye, Zitong
    Yang, Xinxun
    Zhu, Hongfei
    Tang, Mingwei
    Han, Yubing
    Kuang, Cuifang
    Liu, Xu
    APL PHOTONICS, 2024, 9 (03)
  • [6] Recent advancements in structured-illumination microscopy toward live-cell imaging
    Hirano, Yasuhiro
    Matsuda, Atsushi
    Hiraoka, Yasushi
    MICROSCOPY, 2015, 64 (04) : 237 - 249
  • [7] Increasing Resolution in Live Cell Microscopy by Structured Illumination (SIM)
    Richter, Verena
    Piper, Mathis
    Wagner, Michael
    Schneckenburger, Herbert
    APPLIED SCIENCES-BASEL, 2019, 9 (06):
  • [8] Live imaging at 100nm resolution by structured illumination microscopy
    Kner, Peter
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 242
  • [9] Cost-Effective Live Cell Structured Illumination Microscopy with Video-Rate Imaging
    Sandmeyer, Alice
    Lachetta, Mario
    Sandmeyer, Hauke
    Huebner, Wolfgang
    Huser, Thomas
    Mueller, Marcel
    ACS PHOTONICS, 2021, 8 (06) : 1639 - 1648
  • [10] Superresolution live imaging of plant cells using structured illumination microscopy
    Komis, George
    Mistrik, Martin
    Samajova, Olga
    Ovecka, Miroslav
    Bartek, Jiri
    Samaj, Jozef
    NATURE PROTOCOLS, 2015, 10 (08) : 1248 - 1263