Cargando…
Optimal resolution in Fresnel incoherent correlation holographic fluorescence microscopy
Fresnel Incoherent Correlation Holography (FINCH) enables holograms and 3D images to be created from incoherent light with just a camera and spatial light modulator (SLM). We previously described its application to microscopic incoherent fluorescence wherein one complex hologram contains all the 3D...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Optical Society of America
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368318/ https://www.ncbi.nlm.nih.gov/pubmed/21445140 http://dx.doi.org/10.1364/OE.19.005047 |
_version_ | 1782234939117273088 |
---|---|
author | Brooker, Gary Siegel, Nisan Wang, Victor Rosen, Joseph |
author_facet | Brooker, Gary Siegel, Nisan Wang, Victor Rosen, Joseph |
author_sort | Brooker, Gary |
collection | PubMed |
description | Fresnel Incoherent Correlation Holography (FINCH) enables holograms and 3D images to be created from incoherent light with just a camera and spatial light modulator (SLM). We previously described its application to microscopic incoherent fluorescence wherein one complex hologram contains all the 3D information in the microscope field, obviating the need for scanning or serial sectioning. We now report experiments which have led to the optimal optical, electro-optic, and computational conditions necessary to produce holograms which yield high quality 3D images from fluorescent microscopic specimens. An important improvement from our previous FINCH configurations capitalizes on the polarization sensitivity of the SLM so that the same SLM pixels which create the spherical wave simulating the microscope tube lens, also pass the plane waves from the infinity corrected microscope objective, so that interference between the two wave types at the camera creates a hologram. This advance dramatically improves the resolution of the FINCH system. Results from imaging a fluorescent USAF pattern and a pollen grain slide reveal resolution which approaches the Rayleigh limit by this simple method for 3D fluorescent microscopic imaging. |
format | Online Article Text |
id | pubmed-3368318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-33683182012-10-01 Optimal resolution in Fresnel incoherent correlation holographic fluorescence microscopy Brooker, Gary Siegel, Nisan Wang, Victor Rosen, Joseph Opt Express Research-Article Fresnel Incoherent Correlation Holography (FINCH) enables holograms and 3D images to be created from incoherent light with just a camera and spatial light modulator (SLM). We previously described its application to microscopic incoherent fluorescence wherein one complex hologram contains all the 3D information in the microscope field, obviating the need for scanning or serial sectioning. We now report experiments which have led to the optimal optical, electro-optic, and computational conditions necessary to produce holograms which yield high quality 3D images from fluorescent microscopic specimens. An important improvement from our previous FINCH configurations capitalizes on the polarization sensitivity of the SLM so that the same SLM pixels which create the spherical wave simulating the microscope tube lens, also pass the plane waves from the infinity corrected microscope objective, so that interference between the two wave types at the camera creates a hologram. This advance dramatically improves the resolution of the FINCH system. Results from imaging a fluorescent USAF pattern and a pollen grain slide reveal resolution which approaches the Rayleigh limit by this simple method for 3D fluorescent microscopic imaging. Optical Society of America 2011-03-02 /pmc/articles/PMC3368318/ /pubmed/21445140 http://dx.doi.org/10.1364/OE.19.005047 Text en ©2011 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially. |
spellingShingle | Research-Article Brooker, Gary Siegel, Nisan Wang, Victor Rosen, Joseph Optimal resolution in Fresnel incoherent correlation holographic fluorescence microscopy |
title | Optimal resolution in Fresnel incoherent correlation holographic fluorescence microscopy |
title_full | Optimal resolution in Fresnel incoherent correlation holographic fluorescence microscopy |
title_fullStr | Optimal resolution in Fresnel incoherent correlation holographic fluorescence microscopy |
title_full_unstemmed | Optimal resolution in Fresnel incoherent correlation holographic fluorescence microscopy |
title_short | Optimal resolution in Fresnel incoherent correlation holographic fluorescence microscopy |
title_sort | optimal resolution in fresnel incoherent correlation holographic fluorescence microscopy |
topic | Research-Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368318/ https://www.ncbi.nlm.nih.gov/pubmed/21445140 http://dx.doi.org/10.1364/OE.19.005047 |
work_keys_str_mv | AT brookergary optimalresolutioninfresnelincoherentcorrelationholographicfluorescencemicroscopy AT siegelnisan optimalresolutioninfresnelincoherentcorrelationholographicfluorescencemicroscopy AT wangvictor optimalresolutioninfresnelincoherentcorrelationholographicfluorescencemicroscopy AT rosenjoseph optimalresolutioninfresnelincoherentcorrelationholographicfluorescencemicroscopy |