A dual path programmable array microscope (PAM): simultaneous acquisition of conjugate and non‐conjugate images
- 1 November 2001
- journal article
- research article
- Published by Wiley in Journal of Microscopy
- Vol. 204 (2) , 119-135
- https://doi.org/10.1046/j.1365-2818.2001.00945.x
Abstract
A programmable array microscope (PAM) incorporates a spatial light modulator (SLM) placed in the primary image plane of a widefield microscope, where it is used to define patterns of illumination and/or detection. We describe the characteristics of a special type of PAM collecting two images simultaneously. The conjugate image (Ic) is formed by light originating from the object plane and returning along the optical path of the illumination light. The non‐conjugate image (Inc) receives light from only those regions of the SLM that are not used for illuminating the sample. The dual‐signal PAM provides much more time‐efficient excitation than the confocal laser scanning microscope (CLSM) and greater utilization of the available emission light. It has superior noise characteristics in comparison to single‐sided instruments. The axial responses of the system under a variety of conditions were measured and the behaviour of the novel Inc image characterized. As in systems in which only Ic images are collected (Nipkow‐disc microscopes, and previously characterized PAMs), the axial response to thin fluorescent films showed a sharpening of the axial response as the unit cell of the repetitive patterns decreased in size.The dual‐signal PAM can be adapted to a wide range of data analysis and collection strategies. We investigated systematically the effects of patterns and unit cell dimensions on the axial response. Sufficiently sparse patterns lead to an Ic image formed by the superposition of the many parallel beams, each of which is equivalent to the single scanning spot of a CLSM. The sectioning capabilities of the system, as given by its axial responses, were similar for a given scan pattern and for processed pseudorandom sequence (PRS) scans with the same size of the unit cell. For the PRS scans, optical sectioning was achieved by a subtraction of an Inc image or, alternatively, a scaled widefield image from the Ic image. Based on the comparative noise levels of the two methods, the non‐conjugate subtraction was significantly superior. A point spread function for Ic and Inc was simulated and properties of the optical transfer functions (OTFs) were compared. Simulations of the OTF in non‐conjugate imaging did not suffer from the missing cone problem, enabling a high quality deconvolution of the non‐conjugate side alone. We also investigated the properties of images obtained by subjecting the Ic and Inc data to a combined maximum likelihood deconvolution.Keywords
This publication has 25 references indexed in Scilit:
- A His2AvDGFP Fusion Gene Complements a Lethal His2AvD Mutant Allele and Provides an in Vivo Marker for Drosophila Chromosome BehaviorDNA and Cell Biology, 1999
- Equivalence of the Huygens–Fresnel and Debye approach for the calculation of high aperture point‐spread functions in the presence of refractive index mismatchJournal of Microscopy, 1999
- Spectral Imaging in a Programmable Array Microscope by Hadamard Transform Fluorescence SpectroscopyApplied Spectroscopy, 1999
- Optical Sectioning Fluorescence Spectroscopy in a Programmable Array MicroscopeApplied Spectroscopy, 1998
- Image restoration based on Good’s roughness penalty with application to fluorescence microscopyJournal of the Optical Society of America A, 1998
- Theory of confocal fluorescence imaging in the programmable array microscope (PAM)Journal of Microscopy, 1998
- Confocal microscopy by aperture correlationOptics Letters, 1996
- Acceleration of maximum-likelihood image restoration for fluorescence microscopy and other noncoherent imageryJournal of the Optical Society of America A, 1991