Distinct modulated pupil function system for real-time imaging of living cells.

Optical microscopy is one of the most contributive tools for cell biology in the past decades. Many microscopic techniques with various functions have been developed to date, i.e., phase contrast microscopy, differential interference contrast (DIC) microscopy, confocal microscopy, two photon microsc...

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Main Authors: Tomonobu M Watanabe, Yoshikazu Tsukasaki, Hideaki Fujita, Taro Ichimura, Tatsuya Saitoh, Shizuo Akira, Toshio Yanagida
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3433489?pdf=render
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spelling doaj-b3ffdac109634c939231ff1d6efb3e032020-11-25T01:48:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4402810.1371/journal.pone.0044028Distinct modulated pupil function system for real-time imaging of living cells.Tomonobu M WatanabeYoshikazu TsukasakiHideaki FujitaTaro IchimuraTatsuya SaitohShizuo AkiraToshio YanagidaOptical microscopy is one of the most contributive tools for cell biology in the past decades. Many microscopic techniques with various functions have been developed to date, i.e., phase contrast microscopy, differential interference contrast (DIC) microscopy, confocal microscopy, two photon microscopy, superresolution microscopy, etc. However, person who is in charge of an experiment has to select one of the several microscopic techniques to achieve an experimental goal, which makes the biological assay time-consuming and expensive. To solve this problem, we have developed a microscopic system with various functions in one instrument based on the optical Fourier transformation with a lens system for detection while focusing on applicability and user-friendliness for biology. The present instrument can arbitrarily modulate the pupil function with a micro mirror array on the Fourier plane of the optical pathway for detection. We named the present instrument DiMPS (Distinct optical Modulated Pupil function System). The DiMPS is compatible with conventional fluorescent probes and illumination equipment, and gives us a Fourier-filtered image, a pseudo-relief image, and a deep focus depth. Furthermore, DiMPS achieved a resolution enhancement (pseudo-superresolution) of 110 nm through the subtraction of two images whose pupil functions are independently modulated. In maximum, the spatial and temporal resolution was improved to 120 nm and 2 ms, respectively. Since the DiMPS is based on relay optics, it can be easily combined with another microscopic instrument such as confocal microscope, and provides a method for multi-color pseudo-superresolution. Thus, the DiMPS shows great promise as a flexible optical microscopy technique in biological research fields.http://europepmc.org/articles/PMC3433489?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Tomonobu M Watanabe
Yoshikazu Tsukasaki
Hideaki Fujita
Taro Ichimura
Tatsuya Saitoh
Shizuo Akira
Toshio Yanagida
spellingShingle Tomonobu M Watanabe
Yoshikazu Tsukasaki
Hideaki Fujita
Taro Ichimura
Tatsuya Saitoh
Shizuo Akira
Toshio Yanagida
Distinct modulated pupil function system for real-time imaging of living cells.
PLoS ONE
author_facet Tomonobu M Watanabe
Yoshikazu Tsukasaki
Hideaki Fujita
Taro Ichimura
Tatsuya Saitoh
Shizuo Akira
Toshio Yanagida
author_sort Tomonobu M Watanabe
title Distinct modulated pupil function system for real-time imaging of living cells.
title_short Distinct modulated pupil function system for real-time imaging of living cells.
title_full Distinct modulated pupil function system for real-time imaging of living cells.
title_fullStr Distinct modulated pupil function system for real-time imaging of living cells.
title_full_unstemmed Distinct modulated pupil function system for real-time imaging of living cells.
title_sort distinct modulated pupil function system for real-time imaging of living cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Optical microscopy is one of the most contributive tools for cell biology in the past decades. Many microscopic techniques with various functions have been developed to date, i.e., phase contrast microscopy, differential interference contrast (DIC) microscopy, confocal microscopy, two photon microscopy, superresolution microscopy, etc. However, person who is in charge of an experiment has to select one of the several microscopic techniques to achieve an experimental goal, which makes the biological assay time-consuming and expensive. To solve this problem, we have developed a microscopic system with various functions in one instrument based on the optical Fourier transformation with a lens system for detection while focusing on applicability and user-friendliness for biology. The present instrument can arbitrarily modulate the pupil function with a micro mirror array on the Fourier plane of the optical pathway for detection. We named the present instrument DiMPS (Distinct optical Modulated Pupil function System). The DiMPS is compatible with conventional fluorescent probes and illumination equipment, and gives us a Fourier-filtered image, a pseudo-relief image, and a deep focus depth. Furthermore, DiMPS achieved a resolution enhancement (pseudo-superresolution) of 110 nm through the subtraction of two images whose pupil functions are independently modulated. In maximum, the spatial and temporal resolution was improved to 120 nm and 2 ms, respectively. Since the DiMPS is based on relay optics, it can be easily combined with another microscopic instrument such as confocal microscope, and provides a method for multi-color pseudo-superresolution. Thus, the DiMPS shows great promise as a flexible optical microscopy technique in biological research fields.
url http://europepmc.org/articles/PMC3433489?pdf=render
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