super-resolution in confocal microscopy - fhi · (for deep-tissue imaging) 50 % ronald breedijk...

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13/12/2017 1 New modalities in Re-scan Confocal Microscopy (RCM) Erik Manders Innovative Microscopy Lab Swammerdam Institute for Life Science University of Amsterdam and Confocal.nl BV The historical Brakenhoff-confocal (1989) Prof. Brakenhoff Confocal Microscopy Unit 1: Confocal microscope Unit 2: Pinhole + PMT PMT Standard confocal Pinhole 0.2 AU 1.0 AU 4.0 AU Sectioning Resolution SNR Super-resolution SIM STORM STED Confocal Wide-field Abbe’s limit Optical sectioning Labeling density RCM % Unit 1: Confocal microscope Unit 2: Re-scanner + CCD CCD Re-scan Confocal Microscopy (RCM) Giulia De Luca De Luca, et al. (2013) Biomedical Optics Express, 4(11), 2555–2569

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  • 13/12/2017

    1

    New modalities in Re-scan Confocal Microscopy (RCM)

    Erik Manders

    Innovative Microscopy Lab

    Swammerdam Institute for Life Science

    University of Amsterdam

    and

    Confocal.nl BV

    The historical Brakenhoff-confocal (1989)

    Prof. Brakenhoff

    Confocal Microscopy

    Unit 1: Confocal microscope

    Unit 2: Pinhole + PMT

    PMT

    Standard confocal

    Pinhole

    0.2 AU

    1.0 AU

    4.0 AU

    Sectioning Resolution SNR

    Super-resolution

    SIM

    STORM

    STED Confocal

    Wide-field

    Abbe’s limit

    Optical sectioning

    Labeling density

    RCM

    %

    Unit 1: Confocal microscope

    Unit 2: Re-scanner + CCD

    CC

    D

    Re-scan Confocal Microscopy (RCM)

    Giulia De Luca De Luca, et al. (2013) Biomedical Optics Express, 4(11), 2555–2569

  • 13/12/2017

    2

    Re-scan Confocal Microscopy (RCM)

    RCM Standard

    Super resolution: from 245 ± 15 nm to 170 ± 10 nm

    100 nm beads, 100x objective (CFI Apo TIRF 100X Oil, NA 1.49, Nikon)

    De Luca, et al. (2013) Biomedical Optics Express, 4(11), 2555–2569 Giulia De Luca

    Pinhole

    0.2 AU

    1.0 AU

    4.0 AU

    Sectioning Resolution SNR

    Standard confocal

    Pinhole Sectioning Resolution SNR

    0.2 AU

    1.0 AU

    4.0 AU

    RCM Sensitivity helps to see resolution

    Giulia De Luca

    Pinhole Sectioning Resolution SNR

    0.2 AU

    1.0 AU

    4.0 AU

    RCM Confocal Lateral resolution: 240 nm

    RCM Lateral resolution:

    170 nm

  • 13/12/2017

    3

    Jana Doehrner

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    Zheng Chao

    Alexia Loynton-Ferrand

    Alexia Lo

    ynto

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    d

    Leila Nah

    idi

    Thomas Start

    Ro

    nal

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    Zee

    len

    ber

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    Gert van Cappellen Thomas Start

    Jana Doehrner

    Ger

    t va

    n C

    app

    elle

    n

    Zheng Chao

    Live cell RCM imaging

    Ronald Breedijk, Christiaan Zeelenberg and Giulia De Luca

    FRET-RCM

    T=0 is after ~2 hr after adding Staurosporine (2 μM) to a Tag-GFP Tag-RFP Caspase sensor Sample courtesy: Mark Hink, Linda Joosen, UvA

    00.5

    11.5

    0 50 100 150

    time (min)

    FRET ratio

    Giulia De Luca

    NIR-RCM (for deep-tissue imaging)

    50%

    Ronald Breedijk

    Super-resolution

    SIM

    STORM

    STED Confocal

    Wide-field

    Abbe’s limit

    Optical sectioning

    Labeling density

    RCM RCM

  • 13/12/2017

    4

    Deconvolution 130 nm

    Mika Ruonala

    Raw RCM Deconvolved

    RCM-SIM 110 nm

    Ronald Breedijk

    Confocal RCM-SIM

    Rescan Confocal Microscopy (RCM)

    2013 2014

    2015 2016

    Axial: 600 nm @ 488 nm

    Lateral : 170 nm (FWHM @ 488 nm)

    resolution

    up to 4 lasers

    e.g. 405, 488, 561, 638 nm

    four colours

    typical 1 fps @ 512x512 images.

    Higher speed possible for smaller images.

    scanning speed

    C-mount low cost EMCCD/SCMOS QE: 80-95 %

    camera based

    Innovative Microscopy Lab University of Amsterdam

    Ronald Breedijk Giulia De Luca Christiaan Zeelenberg Venkat Kishnaswami Rick Brandt Irene Stellingwerf Emilie Desclos Erik Manders Fred Brakenhoff

    Department of Cell Bio. and Histology, Academic Medical Center Venkat Krishnaswami Ron Hoebe

    Department of Imaging Science & Technology Delft University of Technology Bernd Rieger Sjoerd Stallinga

    Stichting Technologie en Wetenschap “ Ultra-sensitive Conf. Microscopy”

    STW-perspectief progr:am “Nanoscopy”

    Confocal.nl BV, Amsterdam

    Paula Onrust Ronald Breedijk Irene Stellingwerf Stan Hilt Carla Kalkhoven Erik Manders Peter Drent

    Laboratory of Functional and Structural Tissue Imaging, Nencki Institute, Warsaw, Poland Tytus Bernas