Motion artefact detection in structured illumination microscopy for live cell imaging.

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.

[1]  O. Mandula,et al.  Structured illumination microscopy of a living cell , 2009, 2011 International Quantum Electronics Conference (IQEC) and Conference on Lasers and Electro-Optics (CLEO) Pacific Rim incorporating the Australasian Conference on Optics, Lasers and Spectroscopy and the Australian Conference on Optical Fibre Technology.

[2]  X. Fang,et al.  Single-molecule fluorescence imaging in living cells. , 2013, Annual review of physical chemistry.

[3]  Bryant B. Chhun,et al.  Super-Resolution Video Microscopy of Live Cells by Structured Illumination , 2009, Nature Methods.

[4]  W. Michalski,et al.  Correlation between spatial (3D) structure of pea and bean thylakoid membranes and arrangement of chlorophyll-protein complexes , 2012, BMC Plant Biology.

[5]  M. Gustafsson Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy , 2000, Journal of microscopy.

[6]  Jianying Zhou,et al.  Fast structured illumination microscopy using rolling shutter cameras , 2016 .

[7]  Rainer Heintzmann,et al.  Laterally modulated excitation microscopy: improvement of resolution by using a diffraction grating , 1999, European Conference on Biomedical Optics.

[8]  M. Gustafsson,et al.  Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination. , 2008, Biophysical journal.

[9]  Rainer Heintzmann,et al.  Single-shot optical sectioning using polarization-coded structured illumination , 2010 .

[10]  Rainer Heintzmann,et al.  fastSIM: a practical implementation of fast structured illumination microscopy , 2015, Methods and applications in fluorescence.

[11]  Rainer Heintzmann,et al.  Simple structured illumination microscope setup with high acquisition speed by using a spatial light modulator. , 2014, Optics express.