Abstract
Fluorescence microscopy is essential to study biological structures and dynamics. However, existing systems suffer from a trade-off between field of view (FOV), resolution, and system complexity, and thus cannot fulfill the emerging need for miniaturized platforms providing micron-scale resolution across centimeter-scale FOVs. To overcome this challenge, we developed a computational miniature mesoscope (
C
M
2
) that exploits a computational imaging strategy to enable single-shot, 3D high-resolution imaging across a wide FOV in a miniaturized platform. Here, we present
C
M
2
V2, which significantly advances both the hardware and computation. We complement the
3
×
3
microlens array with a hybrid emission filter that improves the imaging contrast by
5
×
, and design a 3D-printed free-form collimator for the LED illuminator that improves the excitation efficiency by 3×. To enable high-resolution reconstruction across a large volume, we develop an accurate and efficient 3D linear shift-variant (LSV) model to characterize spatially varying aberrations. We then train a multimodule deep learning model called
C
M
2
N
e
t
, using only the 3D-LSV simulator. We quantify the detection performance and localization accuracy of
C
M
2
N
e
t
to reconstruct fluorescent emitters under different conditions in simulation. We then show that
C
M
2
N
e
t
generalizes well to experiments and achieves accurate 3D reconstruction across a
∼
7
-
m
m
FOV and 800-µm depth, and provides
∼
6
-
µ
m
lateral and
∼
25
-
µ
m
axial resolution. This provides an
∼
8
×
better axial resolution and
∼
1400
×
faster speed compared to the previous model-based algorithm. We anticipate this simple, low-cost computational miniature imaging system will be useful for many large-scale 3D fluorescence imaging applications.
Funder
National Institutes of Health
Subject
Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials
Cited by
33 articles.
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