Related Experiment Video
Updated: Jun 3, 2025

Conducting Multiple Imaging Modes with One Fluorescence Microscope
Published on: October 28, 2018
Increasing the acquisition speed in oblique plane microscopy via Aliasing
Conor McFadden1, James Manton2, Reto Fiolka1
1Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Oblique plane microscopy (OPM) can be accelerated by controlled under-sampling, enabling faster 3D imaging. This technique recovers aliased data without losing resolution, significantly speeding up subcellular imaging of mitochondrial dynamics.
Area of Science:
- Biomedical Imaging
- Microscopy Techniques
- Cell Biology
Background:
- Oblique plane microscopy (OPM), a variant of light-sheet fluorescence microscopy (LSFM), offers rapid volumetric imaging.
- Current OPM methods require small scanning steps to satisfy Nyquist sampling, limiting acquisition speed and increasing sample exposure.
Purpose of the Study:
- To investigate if controlled under-sampling in OPM can accelerate image acquisition without compromising spatial resolution or introducing artifacts.
- To demonstrate the feasibility of leveraging under-sampling for rapid subcellular 3D imaging.
Main Methods:
- Implementation of controlled under-sampling in an OPM system.
- Development of a recovery method to correct aliasing introduced by under-sampling.
- Application of the accelerated OPM technique for imaging mitochondrial dynamics.
Main Results:
- Judicious under-sampling in OPM leads to recoverable aliasing.
- Spatial resolution and image quality are maintained post-recovery.
- Acquisition speed is increased 2-4 fold, depending on optical parameters.
Conclusions:
- Controlled under-sampling is a viable strategy to enhance OPM acquisition speed.
- This method enables rapid subcellular 3D imaging of dynamic biological processes like mitochondrial movement.
Related Concept Videos
Confocal Fluorescence Microscopy
Aliasing
If the sampling frequency is below the Nyquist rate, these replicas overlap, preventing the original...
Imaging Biological Samples with Optical Microscopy
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
Super-resolution Fluorescence Microscopy
Phase Contrast and Differential Interference Contrast Microscopy
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...
Atomic Force Microscopy
The AFM Probe
The probe is regarded as the heart of any AFM setup and comprises the...

