Affiliation:
1. University Hospital of North Norway
2. UiT The Arctic University of Norway
Abstract
Multifocus microscopy enables recording of entire volumes in a single
camera exposure. In dense samples, multifocus microscopy is severely
hampered by background haze. Here, we introduce a scalable multifocus
method that incorporates optical sectioning and offers improved axial
resolution capabilities. In our method, a dithered oblique light-sheet
scans the sample volume during a single exposure, while fluorescence
from each illuminated plane in the sample is mapped onto a line on the
camera with a multifocus optical element. A synchronized rolling
shutter readout realizes optical sectioning. We describe the technique
theoretically and verify its optical sectioning and resolution
improvement capabilities. We demonstrate a prototype system with a
multifocus beam splitter cascade and record monolayers of endothelial
cells at 35 volumes per second. We furthermore image uncleared
engineered human heart tissue and visualize the distribution of
mitochondria at high axial resolution. Our method manages to capture
sub-diffraction sized mitochondria-derived vesicles up to 30 µm deep
into the tissue.
Funder
Universitetet i
Troms#x00F8;
H2020 European Research
Council
Norges Forskningsråd
Subject
Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials
Cited by
11 articles.
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