New 2D Superresolution mode for ZEISS Airyscan delivers 120 nanometer lateral resolution

New 2D Superresolution mode for ZEISS Airyscan delivers 120 nanometer lateral resolution


Improved optical sectioning brings higher resolution without acquiring a z-stack

At Neuroscience 2017, a new processing mode for the ZEISS LSM 8 family with Airyscan has been introduced. ZEISS Airyscan allows for the unique combination of superresolution imaging with increased sensitivity and acquisition speed. It works with standard samples and dyes, and captures 3D data even in thicker samples that need a higher penetration depth. The unique 32-channel GaAsP array detector captures more spatial information than traditional confocal microscopes. The new 2D Superresolution mode now uses this additional information to create an optical section of 0.2 Airy units (AU) and resolves structures down to 120 nanometer laterally in a single image.

The benefits for scientists

In the past, researchers had to acquire a stack of z-slices and subsequently deconvolve to get optical sections thinner than one AU and enhance lateral resolution. Temporal resolution was thus limited, and a prolonged light exposure of the sample was inevitable. Scientists can now use the new 2D Superresolution mode to overcome this problem and perform gentle live cell imaging experiments. They profit from very low light exposure, highly resolved structural information and excellent signal-to-noise ratio.

Confocal image (left) / Airyscan image (right). Cells labelled with TOMM20 – Alexa Fluor 488 (green) and TIMM – Alexa Fluor 568

The principle behind

ZEISS Airyscan is an area detector. Unlike traditional confocal microscopes which reject photons from outside of the focal plane at a pinhole, ZEISS Airyscan detects all precious fluorescence emission photons of 1.25 AU. Their information is then used to deliver higher sensitivity, superresolution, and high acquisition speeds. The new 2D Superresolution mode takes advantage of the fact that ZEISS Airyscan captures x, y and z information of the confocal point spread function. A new exclusive processing algorithm uses this inherent spatial information captured in a single image. It specifically distinguishes between photons originating from the focal plane of 0.2 AU and photons from outside of this focal plane. In a traditional confocal microscope, a researcher could only close the pinhole to 0.2 AU to attempt to achieve the same optical sectioning. This would mean sacrificing many photons, even from the focal plane, thus reducing signal-to-noise drastically.
Researchers can process both existing and new ZEISS Airyscan data with the new 2D Superresolution mode.

More information on ZEISS LSM 880 with Airyscan

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Carl Zeiss

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